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Moving battery technology from the laboratory to large-scale production is a necessary step in achieving cost competitiveness for high-energy-density batteries
academic research has focused on the active material of the electrode and little attention has been paid to cell-level design
upscaling high-areal-capacity electrode sheets is proposed as a practical way forward
Here we evaluate the impact of high-areal-capacity electrodes on cell energy densities
energy consumption during electrode fabrication and the cost efficiency of cell production
By examining the integration of scalable roll-to-roll electrode-manufacturing techniques (such as slurry casting and dry coating) with the materials chemistry of the electrode components
electrode structure design and cell performance
we aim to outline the areas of development for high-areal-capacity electrodes and provide a structured pathway for bridging the gap between laboratory innovations and industrial scale-up
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This work was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT (RS-2024-00344021 and RS-2024-00455177) and LG Energy Solution
acknowledges the support from the Center for Mesoscale Transport Properties
an Energy Frontier Research Center supported by the US Department of Energy
as well as from the Welch Foundation F-1861
These authors contributed equally: Jung-Hui Kim
Department of Chemical and Biomolecular Engineering
Materials Science and Engineering Program and Walker Department of Mechanical Engineering
investigated the industrial electrode manufacturing processes
performed the specific energy and cost analyses of the cells
conducted the theoretical calculations of cell performance
conducted the literature studies on slurry-cast electrode processing
carried out the literature studies on dry-coated electrode processing
performed the literature studies on alternative electrode-processing methods
All authors contributed to the writing and revision of the manuscript
The authors declare no competing interests
Matthew Li and Moumita Rana for their contribution to the peer review of this work
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations
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How biological neural networks reliably process information in the presence of spontaneous activity remains controversial
stimulus-evoked and spontaneous activity show orthogonal (dissimilar) patterns
which is advantageous for separating sensory signals from internal noise
have reported high similarity between stimulus-evoked and spontaneous activity
the mechanism of signal-noise separation in the columnar visual cortex may be different from that in rodents
we compared spontaneous and stimulus-evoked activity in marmoset V1 and higher visual areas
spontaneous and stimulus-evoked activity showed similar patterns as expected
spontaneous and stimulus-evoked activity were progressively orthogonalized along the cortical hierarchy
eventually reaching levels comparable to those in mouse V1
These results suggest that orthogonalization of spontaneous and stimulus-evoked activity is a general principle of cortical computation
the fact that both sets of studies were conducted only on V1 makes it difficult to extend these results to general cortical computations
if spontaneous and evoked activities share similar patterns in all the visual areas of carnivores/primates
it would be of great interest to determine how the cortical network could distinguish between stimulus-related information from internally generated noise
To systematically characterize the spatiotemporal patterns of spontaneous activity across the marmoset visual areas
we used a newly developed primate-optimized expression system of genetically encoded calcium indicators (Hashimoto et al.
these results suggest that the patchy activity pattern is a canonical mode of spontaneous activity in the primate neocortex
a Two-photon calcium imaging is conducted in visual areas identified from widefield imaging
spontaneous and visually evoked activity is recorded for the identical set of cells
b Example cell image and cellular orientation map in V1
Experiments were repeated in 12 times and similar results were obtained
The cellular orientation map is calculated using the cells identified from the cell image (left)
c Time courses of spontaneous activity for example cells
Comparison of spontaneous and evoked activity in V1 (d)
Timecourses” shows a correlation between individual spontaneous frames and responses to single orientations or directions
Panel “FOV Activity” shows the average activity of all the cells in the FOV
Resp.” show an example spontaneous frame and a response to a single orientation that is most similar to the spontaneous frame
Two examples are shown for time points indicated by dotted lines in the time courses
g Cumulative plots showing the similarity of spontaneous frames and evoked activity
correlations with all single orientation or direction responses are calculated
a summary table of statistically significant difference [*
p < 0.05 (corrected by Bonferroni’s method)
the correspondence did not apply to downstream area MT
suggesting that the relationship between spontaneous and evoked activity varies across cortical areas
a Overview of the analysis based on cellular-level neural activity data recorded by two-photon imaging
Trial-averaged visual responses are projected to a space spanned by spontaneous activity to obtain activity patterns shared by spontaneous and evoked activity (Shared Activity)
Trial-averaged visual responses are orthogonalized to the space spanned by spontaneous activity to activity patterns specific to stimulus-evoked activity (Stim-Only Activity)
Spontaneous activities were orthogonalized to a space spanned by trial-averaged visual responses to obtain activity patterns specific to spontaneous activity (Sponta-Only Activity)
b Examples of the 1st principal components (PCs; left panels
blue-to-yellow colour) of activity patterns in the three activity-spaces
a single condition visual response that is most similar is also shown (right
Correlation coefficients between pairs of PC and visual response: V1 Shared (0.29)
c Population data on the similarity between PCs and visual responses
Horizontal lines indicate pairs with significant differences (p < 0.05
corrected by Bonferroni’s method for 6 pairwise comparisons)
N numbers indicating number of FOVs are 12(V1)
two-sided) are as follows: 0.339 (Stim-Only
To quantify the contribution of the averaged signals to the total variance in single-trial neural activity, we performed a cross-validated regression of neural activity. In the marmosets V1, V2, MT and mouse V1, the percent of the total variance of single-trial activity explained by the averaged signals ranged between 30 and 50% (Supplementary Fig. 8)
the trial-averaged neural activity explained a substantial fraction of the single-trial stimulus-evoked responses in all tested visual areas
a Variance of cellular-level trial-averaged visual responses projected to the Shared subspace
Horizontal lines indicate pairs with significant difference (p < 0.01
b Same as (a) but projected to individual PCs of Shared Space
c Variance of single trial visual responses (left) and spontaneous activity (right) projected to each subspace
and are same for all subspaces and trial-types
Spontaneous and visually evoked activities in the primate visual cortex are progressively orthogonalized along the hierarchical network
The degree of the orthogonality in the mouse V1 is similar to higher but not lower visual areas of the marmoset
The estimated dimensionality of shared space, as quantified by the number of PCs with large projections of stimulus-related variance, showed a similar tendency to the amount of projected variance; the dimensionality of shared space was larger for marmosets V1 and V2 than for marmoset MT and mouse V1 (Supplementary Fig. 12a)
the overlap between spontaneous and evoked activity progressively decreased along the cortical hierarchy
these results suggest that the marmoset visual network achieves the separation of stimulus-related signal information and internally generated noise through processing in the hierarchical cortical areal network
the presence of patchy spatial patterns may indicate that spontaneous activity propagates along cortico-cortical connections
It is of great interest for future studies to examine whether the relationship between the spontaneous and evoked activity in the mouse V1 and the marmoset MT follows a similar developmental pattern
It is likely that the anaesthetic condition used in the present study strongly attenuated this component of neuronal activity (in fact the variance projected to the 1st PC in our data was 8% whereas that in Stringer et al
Because almost all of the visual areas are accessible for optical recording and manipulation
the marmoset monkey is ideally suited for testing these hypotheses
It is tempting to speculate that the difference in the site of orthogonalization in the marmoset and the mouse is related to the difference in the depth of the hierarchical cortical network in the two species: the marmoset with a deep cortical network may benefit initially parallel spontaneous activity
whereas the mouse with a shallow cortical network benefit more by having orthogonalized spontaneous activity already at V1
despite the species difference in circuit-level implementations
the orthogonalization of activity patterns is likely a common computational goal for separating sensory signals and internal noise in biological neural circuits
A total of 12 adult common marmosets (Callithrix jacchus; 7 males and 5 females; body weight
1–2 years) obtained from Nihon Clea and four Thy1-GCaMP6 mice (4 males; GP 4.3
P50–60) obtained from Jackson Laboratory were used
All animals were housed in a 12:12 h light-dark cycle
had access to water and food ad libitum and were not used for other experiments before the present study
All animal experiments were carried out following the institutional welfare guidelines laid down by the Animal Care and Use Committee of the University of Tokyo
and approved by the Ethical Committee of the University of Tokyo
10 were used to obtain widefield imaging data [Large FOV covering the occipital-parietal cortex
and nine were used to obtain two-photon imaging data [V1
Four mice were used to obtain the two-photon imaging data (12 FOVs in V1)
pAAV-TRE-GCaMP6f-WPRE was used as a template for this plasmid
AAV plasmids were packaged into AAV serotype 9 using the AAV Helper-Free system (Agilent Technologies)
and pHelper plasmids were transfected into HEK293 cells
AAV2/9 particles were purified using the AAV Purification kit (Takara
The AAV solution was concentrated to the optimal volume by centrifugation using an Amicon Ultra-4 100k centrifugal filter unit (Millipore)
The number of genomic copies was quantified with intercalating dyes (Thermo Fisher Scientific
USA) and two sets of primers for WPRE or hGHpA genes
The final titration of the AAV was estimated as relative quantitation according to a calibration curve calculated from the known numbers of copies of AAV plasmids
All surgical procedures were performed under aseptic conditions
Marmosets were anaesthetized with isoflurane (4.0–5.0% for induction and 1.5–3.0% for maintenance in a mixture of 20–50% O2 and air)
percutaneous oxygen saturation (SpO2) and heart rate were monitored and maintained at >96% and <200 bpm
The rectal temperature was maintained at 37 °C using an electric blanket and a feedback-controlled heating pad
s.c.) was administered as an antibiotic prophylaxis
s.c.) was administered to reduce pain and inflammation
The scalp was sterilized with povidone-iodine
All incision sites were pre-treated with local injections of lidocaine HCl (2%) or lidocaine jelly
a custom-made metal head post was attached to the skull using dental acrylic (Shofu Inc.)
Marmosets were then head-fixed on a custom-made metal stage using a head post
1–2 mm apart) were made around the targeted cortical regions
and the dura mater was cut to expose the cortical surface
The brain was washed with gentamycin-mixed artificial cerebrospinal fluid (ACSF)
An AAV cocktail with a 1:1 mixture of AAV2/9-Thy1S-tTA (3.11 × 1013 vg/ml) and AAV2/9-TRE-tandem-GCaMP6s (2.65 × 1013 vg/ml) was loaded into a glass pipette and injected using a Nanoject III (Drummond Scientific Company)
The pipette was inserted 300–500 µm below the cortical surface
and 0.5–1.0 µl AAV was injected at 0.12 µl/min in a single injection site
the craniotomies were covered with Kwik-SilTM (World Precision Instruments)
All wound sites were treated with gentamycin ointment
warmed physiological saline (5 ml) was administered subcutaneously to prevent dehydration
and the animals were returned to their home cage for recovery
meloxicam and/or ampicillin were/was administered for postoperative management
The animals were maintained for 4–5 weeks before the imaging experiments to ensure sufficient GCaMP expression
s.c.) was administered as an anti-inflammatory drug
and the animal was mechanically ventilated
End-tidal CO2 was monitored and kept at 3.4–4.0% throughout the experiment
An intravenous catheter was placed in the femoral vein
and anaesthesia was maintained by constant infusion of remifentanil (6.0–15.0 μg/kg/h
i.v.) mixed in lactated Ringer’s solution (2.0 ml/kg/h) and dexamethasone (0.4 mg/kg/h)
Muscle relaxation was induced by vecuronium bromide (0.1 mg/kg/h
Additional doses of isoflurane (2.0%–3.0%) and N2O (50% in O2 and air) were administered intraoperatively
A custom-made metal head post was attached to the skull
and the animal was mounted on a stereotaxic apparatus
A large cranial window was made over the targeted brain regions (12 mm diameter circle or 8 mm × 16 mm square
A glass coverslip (10 mm in diameter or 8 mm × 16 mm square) attached to a custom-made metal rim was placed on the exposed cortical surface
and the brain was sealed with Kwik-SilTM (World Precision Instruments) and dental cement (Sun Medical)
anaesthesia was maintained by remifentanil (6.0–15.0 μg/kg/h
and doses of isoflurane and N2O were decreased to 0–0.5% and 10–50%
The eyes were covered with contact lenses and frequently moistened with an ophthalmic solution to ensure a clear view throughout the experiment
In vivo wide-field imaging was performed using a macrozoom fluorescence microscope (MVX10
Olympus) equipped with a 2× objective (2x MVX Plan Apochromat Lens
GCaMP was excited by a mercury lamp through a GFP mirror unit (U-MGFPHQ/XL
Fluorescence images were acquired using an sCMOS camera (Zyla 4.2 sCMOS
Andor Technology) controlled by NIS Elements BR (Nikon)
A square region of the cortex (6 × 6 mm to 15 × 15 mm
512 × 512 or 256 × 256 pixels) was imaged at 5 Hz
the animals were moved under a two-photon microscope (A1RMP
Japan) equipped with a water immersion objective (16× or 25× with NA 0.8 or NA 1.1
Nikon) to perform two-photon calcium imaging
GCaMP was excited at a 920-nm wavelength using a Ti:sapphire laser (Mai Tai HP DeepSee
A square region of the cortex (800 μm × 800 μm in 512 × 512 pixels with a 16× objective for marmosets; 500 μm × 500 μm in 512 × 512 pixels with a 25× objective for mice) was imaged at 2 Hz
The position of the FOV was selected from the functional map obtained using widefield imaging
The spatial pattern of blood vessels on the cortical surface was used to guide the FOV
The depth of the imaged plane was carefully adjusted manually between the scans
Image planes from the same cortical location were separated by at least 30 μm in depth to avoid imaging the same neurons twice
Visual stimuli were generated using custom-written programs in PsychoPy72
A 32-inch LCD monitor with a 60-Hz refresh rate (ME32B
Samsung) was positioned 30 cm in front of the marmosets
The stimulus screen spanned −35.6° to 35.6° horizontal and −50.7° to 50.7° vertical of the animal’s visual field
a drifting square-wave grating [100% contrast; 0.5–1 cycle per degree (cpd); 2 Hz] tilted at one of four to eight orientations in equal steps
moving in one of two directions orthogonal to the orientation was presented
we presented a drifting square-wave grating [100% contrast; 0.5–1 cpd; 2 Hz] tilting at one of four to eight orientations in equal steps and moving in one of two directions orthogonal to the orientation
[20 °/s] moving in one of eight or twelve directions in equal steps were used
Each stimulus started with a blank period of uniform grey (4 s) followed by the same period of visual stimulation
Each condition was repeated 20–100 times in pseudorandom orders
In both the widefield and two-photon imaging experiments
spontaneous activity was recorded separately from the visually evoked responses in the dedicated scans
During scans for spontaneous activity recordings
the LCD monitor used for visual stimulation was turned off
we conducted a spontaneous activity scan either before or after the visual stimulus scans
The interval between the two scans was no longer than 30 min
All analyses were performed using custom-written programs in MATLAB (MathWorks
small drifts between the imaging frames were realigned by maximizing the correlation between the images
The relative change in fluorescence (ΔF/F) was computed using the following equation: ΔF/F = (F − F0)/F0
F0 is the average fluorescence during the pre-stimulus period (baseline)
and F is the fluorescence during stimulus presentation
and F is the fluorescence during spontaneous activity
images or time courses were sorted by stimulus conditions and averaged across all repetitions
single-condition maps to the tested orientation (or directions of motion) stimuli were obtained by calculating the relative change in fluorescence (ΔF/F) between the baseline (1 s before stimulus onset) and the stimulus period (4 s)
Each map was high-pass filtered by subtracting the low spatial frequency background
which was obtained by applying 2D median filters three times (kernel size: 0.45 mm by side) to the original map
Direction preference maps (HLS maps) were obtained from single-condition maps
hue (H) represents the preferred orientation or direction calculated by vector averaging
saturation (S) represents the global measure of orientation or direction tuning
which corresponds to 1 − CV (circular variance in orientation or direction preference)
and lightness (L) represents the response to the best direction (ΔF/F)
we first searched for a spontaneous PC that best correlated with the visually evoked activity
We chose to analyse widefield imaging data covering V1 and V2 in the same FOV because these data allowed us to compare the two cortical areas without being affected by differences in animals and/or other experimental conditions
Autocorrelation analysis was performed separately for V1 and V2
and the sizes of the two autocorrelation profiles were compared
Because this analysis used widefield imaging data obtained from one FOV per animal
we did not have sufficient data to perform statistical testing
we set the number of pixels allocated to each cell to 100 for both mice and marmosets
To compare visually evoked and spontaneous activity patterns
we selected FOVs (1) with stable recordings of both visual stimulation scan and spontaneous activity scan and (2) with sufficiently large number of active cells (>100)
we did the same calculation for the position-shuffled control
The clustering index for the plane was defined as the value obtained for the position-shuffled control divided by the value obtained for the real data
we set the number of cells and trials to be equal across all FOVs by randomly selecting 400 cells and 20 trials in each FOV
neural activity was averaged across trials
We treated each frame of the trial-averaged visual evoked response as an individual visual response pattern (frames corresponding to the stimulus-off periods were discarded)
Depending on the number of orientations/directions tested
the total number of trial-averaged visual responses for each set of stimuli ranged from 32 to 64
The frames in which visual stimuli were presented were then collected and denoted as trial-averaged visual responses
producing a matrix \({M}_{{vis}}\) of trial-averaged visually evoked activity with dimension \({N}_{{neuron}}\,\times \,{N}_{{stim}}\)
we used half of the trials to obtain \({M}_{{vis}}\)
and spared the other half of the trials for later calculation of the projected variance of the visually evoked activity
which is a matrix \({N}_{{neuron}}\,\times \,{N}_{{spont}-{frame}},\) was subjected to PCA
and the first 50 PCs were retained (\({{PC}}_{1}^{{spont}},\,{{PC}}_{2}^{{spont}}\ldots \,{{PC}}_{50}^{{spont}}\))
\({N}_{{neuron}}\) was the same for the visually evoked activity and spontaneous activity
The stimulus-only activity \({M}_{{vis}-{only}}\) was obtained by regressing out 50 spontaneous PCs from each column of the trial-averaged visual response
each column \({e}_{i}\) in \({M}_{{vis}-{only}}\) is orthogonal to the spontaneous PCs
The matrix of shared activities \({M}_{{shared}}\) was obtained by projecting each column \({v}_{i}\) of the trial-averaged visual responses \({M}_{{vis}}\) onto 50 spontaneous PCs
each column \({w}_{i}\) of the shared activity \({M}_{{shared}}\) is contained in the space spanned by 50 spontaneous PCs:
The matrix of spontaneous-only activity \({M}_{{spont}-{only}}\) was obtained by regressing out each column \({v}_{i}\) of the trial-averaged visual responses \({M}_{{vis}}\) from each column (i.e.
frame) \({s}_{i}\) of spontaneous activity \({M}_{{spont}}\)
each column \({u}_{i}\) of the spontaneous-only activity \({M}_{{spont}-{only}}\) was orthogonal to each column \({v}_{j}\) of the visually evoked activity \({M}_{{vis}}\):
and the PCs of the shared space were obtained by finding a sequence of orthogonal directions \({a}_{i}\) that maximized the sum of squares of the trial averaged visual response \({M}_{{vis}}\):
Note that the choice of 50 PCs at the initial step for constructing Shared Space could have resulted in underestimation of the number of remaining PCs in each subspace
trial-to-trial variability of single-trial visually evoked responses in our data likely contained both visually related variability and spontaneous activity-related components
We believe that some of the latter components were projected onto the sponta-only PC
Regarding the non-zero projected variance on stim-only PCs in the spontaneous block
we believe that this was because we projected out the top 50 PCs of spontaneous activity
The residual PCs of spontaneous activity that were not used to define stim-only space could have contributed to the projection to the stim-only space
Statistical tests were conducted using Statistics Toolbox in Matlab
Independent group comparisons were performed using two-sample Kolmogorov-Smirnov tests
No statistical methods were used to pre-determine sample sizes
but our sample sizes were similar to those used in previous studies
Allocation in the experimental groups was not randomized
Data collection and analysis were not blinded to experimental conditions
Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article
Minimum dataset that are necessary to interpret, verify and extend the research in the article are available from the corresponding authors. Example data can be downloaded in FigShare (doi:10.6084/m9.figshare.25448167). Source data are provided with this paper
The codes used in this study are available from the corresponding authors. Example codes can be downloaded in GitHub (https://github.com/teppei-matsui/NN_Simulation)
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Task-free MRI predicts individual differences in brain activity during task performance
Distributed network interactions and their emergence in developing neocortex
Spontaneous events outline the realm of possible sensory responses in neocortical populations
Playing the piano with the cortex: Role of neuronal ensembles and pattern completion in perception and behavior
Ongoing physiological processes in the cerebral cortex
Spontaneous behaviors drive multidimensional
Fundamental bounds on the fidelity of sensory cortical coding
Single-trial neural dynamics are dominated by richly varied movements
Small modulation of ongoing cortical dynamics by sensory input during natural vision
Spontaneous cortical activity reveals hallmarks of an optimal internal model of the environment
Shape and arrangement of columns in cat’s striate cortex
Receptive fields and functional architecture of monkey striate cortex
Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex
Homeostatic regulation of eye-specific responses in visual cortex during ocular dominance plasticity
The marmoset monkey as a model for visual neuroscience
A simpler primate brain: The visual system of the marmoset monkey
Long-term two-photon calcium imaging of neuronal populations with subcellular resolution in adult non-human primates
Arm movements induced by noninvasive optogenetic stimulation of the motor cortex in the common marmoset
Chronic multiscale imaging of neuronal activity in the awake common marmoset
Generation of transgenic marmosets expressing genetically encoded calcium indicators
Local homogeneity of tonotopic organization in the primary auditory cortex of marmosets
Optical imaging of functional organization of V1 and V2 in marmoset visual cortex
Paper presented at the Society for Neuroscience
Transient neuronal coactivations embedded in globally propagating waves underlie resting-state functional connectivity
Interhemispheric synchrony of spontaneous cortical states at the cortical column level
Corticocortical connection patterns reveal two distinct visual cortical areas bordering dorsal V2 in marmoset monkey
Spontaneous infra-slow brain activity has unique spatiotemporal dynamics and laminar structure
Columnar specificity of intrinsic horizontal and corticocortical connections in cat visual cortex
Relationship between intrinsic connections and functional architecture revealed by optical imaging and in vivo targeted biocytin injections in primate striate cortex
Orientation selectivity and the arrangement of horizontal connections in tree shrew striate cortex
Organization of horizontal axons in the inferior temporal cortex and primary visual cortex of the macaque monkey
Interdigitation of contralateral and ipsilateral columnar projections to frontal association cortex in primates
Measuring and interpreting neuronal correlations
Mixed functional microarchitectures for orientation selectivity in the mouse primary visual cortex
Orientation selectivity and the functional clustering of synaptic inputs in primary visual cortex
Ultrasensitive fluorescent proteins for imaging neuronal activity
Functional specificity of local synaptic connections in neocortical networks
Stimulus contrast modulates functional connectivity in visual cortex
Dimensionality in recurrent spiking networks: Global trends in activity and local origins in connectivity
The role of population structure in computations through neural dynamics
Spontaneous and evoked activity patterns diverge over development
Population rate dynamics and multineuron firing patterns in sensory cortex
Effects of attention on orientation-tuning functions of single neurons in macaque cortical area V4
A hierarchy of intrinsic timescales across primate cortex
Natural grouping of neural responses reveals spatially segregated clusters in prearcuate cortex
Implications of neuronal diversity on population coding
Correlated neuronal discharge rate and its implications for psychophysical performance
The effect of correlated variability on the accuracy of a population code
The ‘Ideal Homunculus’: decoding neural population signals
The effect of noise correlations in populations of diversely tuned neurons
Population coding in neuronal systems with correlated noise
Population-level neural codes are robust to single-neuron variability from a multidimensional coding perspective
Cortical areas interact through a communication subspace
Reverberation of recent visual experience in spontaneous cortical waves
Computational account of spontaneous activity as a signature of predictive coding
Separate body- and world-referenced representations of visual space in parietal cortex
Transformations of sensory information in the brain reflect a changing definition of optimality
Simultaneous multi-area recordings suggest that attention improves performance by reshaping stimulus representations
Cell-type-specific thalamocortical inputs constrain direction map formation in visual cortex
Generating stimuli for neuroscience using PsychoPy
Similarity of visual selectivity among clonally related neurons in visual cortex
Functional heterogeneity in neighboring neurons of cat primary visual cortex in response to both artificial and natural stimuli
The marmoset brain in stereotaxic coordinates
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We thank members of the Ohki laboratory and Dr
Watakabe for providing pAAV-Thy1S-tTA and pAAV-TRE-GCaMP6f; Drs
Matsuizaki for technical advice; The Genetically-Encoded Neuronal Indicator and Effector (GENIE) Project for providing GCaMP6f/s
This work was supported by Brain/MINDS and Brain/MINDS2.0 from AMED (14533320
Hirai and the Brain/MINDS AAV vector core); Institute for AI and Beyond (to K.O.); CREST-JST (JPMJCR22P1 to K.O.)
Murakami); JSPS Research Fellowship for Young Scientist (20J12796 to T.H.)
Brain/MINDS-beyond from AMED (JP20dm0307031 to T
These authors contributed equally: Teppei Matsui
International Research Center for Neurointelligence (WPI-IRCN)
developed and provided GCaMP expression systems optimized for primates
wrote the manuscript with contributions from all authors
Nature Communications thanks Jorrit Montijn and the other
reviewer(s) for their contribution to the peer review of this work
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DOI: https://doi.org/10.1038/s41467-024-54322-x
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This paper presents a novel method for the measurement of nanometer-scale surfaces
The proposed technique takes advantage of the spin hall effect of light (SHEL)
which occurs as a sub-wavelength beam shift due to the spin-orbit interaction of light when it interacts with non-homogeneous optical media
Governed by the conservation of total angular momentum
the SHEL offers a sensitive approach to detecting the variations of optical properties at an interface
“SHEL Ellipsometry” applies weak measurement principles to observe beam shifts
which analyzes the polarization states of incident and reflected light
a homogeneous sample with surface roughness less than a tenth of the wavelength can be modeled as a thin film characterized by an equivalent thickness and refractive index
By measuring the transverse shifts of the reflected beam and using raster scanning
SHEL Ellipsometry can map the two-dimensional surface roughness distribution
showing significant potential for nanometer-scale surface measurement
Despite the significant progress in fabrication technologies
both in achieving angstrom-scale smoothness and complex nanostructures
the development of nanoscale surface instruments has lagged
Both techniques indirectly infer the surface and material properties of the illuminated area
making them beneficial for fast large-scale measurements of nanoscale surfaces
which are well-suited for industrial applications
it has become easier to study the behavior and the application of this confined beam anomaly
SHEL observation with weak measurement is realized by defining the polarization state of the incident and reflected beam in a way similar to ellipsometry measurement
similar to scatterometry and traditional ellipsometry
the optical properties of an observed surface can influence the measured transverse shift
providing insights into the surface characteristics
By incorporating SHEL with weak measurement and using the effective medium approximation (EMA) as a data analysis tool
SHEL ellipsometry has the potential as an imaging tool that can give nanoscale surface information
This paper offers a novel nanoscale surface characterization using the SHEL ellipsometry
The measurement is done by measuring the SHEL shift of reflected light from the sample in an oblique incidence setup
The SHEL shift is amplified by the weak measurement and recorded using a CCD camera
A two-dimensional reconstruction of the surface was also obtained through raster scanning
which completely avoids errors sourced from the retarder’s rotation or temperature dependence
further offering good stability for long-term measurement
two different interface models are introduced: based on the Fresnel model that returned the parameter as pseudo refractive index and based on the effective medium approximation to obtain equivalent effective thickness
a comparison of pseudo refractive index and known refractive indices of several optics is presented as a result of static single-point measurements
comparative scanning results are also presented to show the potential of SHEL ellipsometry as a novel nanoscale surface measurement
Principle of the spin hall effect of light at an interface, a linearly polarized incident beam will be reflected with different direction of circularly polarized light and transversely shifted at a distance of \(\delta _r\). The 3D image was created using Microsoft PowerPoint version 16.93.2, Microsoft Corporation, (https://www.microsoft.com/powerpoint)
which inherently carries information about the interface
any change in the physical properties at the interface will be reflected as a change in the Fresnel reflection coefficients
a complex weak value amplifies the weak interaction through the predetermined initial and final states
the initial and final states correspond to the selection of the light polarization state upon incidence and reflection
Figure 2 shows the schematic setup for SHEL ellipsometry based on SHEL observation using weak measurement
Polarizer pairs realize the weak measurement through the definition of light polarization as the initial \(|i\rangle\) and final state \(|f\rangle.\)
(inset) polarizer state corresponding to the weak measurement’s requirement
the first-order amplified SHEL shift for a horizontally polarized incident is denoted by:
where \(f_1\) and \(f_2\) correspond to the pair of lenses in Fig. 2 and \(w_{o}\) is the beam diameter at the laser outlet that relates to the propagation factor of the SHEL shift
There are several approaches to improve the model inaccuracy in the vicinity of Brewster’s angle for the \(|H\rangle\) incident
by performing Taylor expansion of the reflection coefficient or by improving the weak measurement model
and the amplified SHEL shift for \(|H\rangle\) incident is denoted by:
once the amplified SHEL shift is observed and the experimental parameters are known
\(\rho\) is used to calculate the physical parameters
The simplest model of an interface in optics is the air-glass interface
where light propagates from air to a more condensed medium
resulting in a change of refractive index along the propagation trajectory
and \(\rho\) is defined using Snell’s Law and the Fresnel formulas as:
The air-glass interface is assumed to be ideal, without any roughness, and \(\rho\) is simply defined as the ratio of Fresnel reflection coefficients p over s, referred here as the Fresnel model. Referring to the sample in Fig. 1
the refractive index of the air is \(n_0\) while the ideally smooth sample’s refractive index is \(n_2\)
which is retrieved from SHEL measurements and is also addressed as the “pseudo” refractive index
Numerical calculation of SHEL shift to incident angle on different refractive index (a) horizontally polarized incident beam and (b) vertically polarized incident beam
Numerical calculation for the horizontally polarized incident on SiO\(_2\) flat windows with various levels of roughness d\(_{EMA}\) (colored lines) compared to Fresnel smooth surface (black line) (a) original SHEL shift and (b) amplified SHEL shift due to weak measurement based on Eq. 5
The experiment procedure is started by setting the sample stage and detection arm to form the desired incident angle
the pair polarizer is set exactly perpendicular to each other or in a cross polarizer state
without the small \(\varepsilon\) angle in P2
This state is essential to observe the splitting beam condition where two symmetrical intensities of SHEL beams appear
The dark fringe between the two intensities is defined as the datum for measuring the SHEL shift
the \(\varepsilon\) is added to the P2 to start the weak measurement
both static measurement and scanning measurement can be performed
The scanning measurement is performed by raster scanning through moving the \(xy\) translation stage
Accuracy check by single point pseudo refractive index measurement of (a) samples consisting of flat windows of different material MgF\(_2\) (\(n = 1.37\))
(b) measurement result of horizontally polarized incident beam
(c) measurement result of vertically polarized incident beam
the results from the \(|H\rangle\) incident measurements are more accurate compared to the known values than those from the \(|V\rangle\) incident measurements
The trend of the measurement results using \(|H\rangle\) also shows agreement with the actual value of the refractive index
the \(|V\rangle\) incident with \(\varepsilon = 0.3^\circ\) and \(0.5^\circ\) shows a false trend and fails to retrieve the correct value of the refractive index
The \(|V\rangle\) incident is more susceptible to error due to the small value of shift
the shift difference due to varying medium properties will be even smaller
Although the \(|V\rangle\) incident is inherently not limited by Brewster’s angle of the sample
the tiny range of shift value in this proposed setup makes it a less favorable option
This experiment demonstrates the potential of SHEL ellipsometry in retrieving the physical properties of samples
as confirmed by comparing the pseudo-refractive index to the known refractive index of the samples
it can be seen that as the post-selected angle increases
the accuracy also improves and becomes closer to the ideal trend line
A static measurement was carried out for varying incident angles to further understand the SHEL observation using weak measurement
both from the perspective of the weak measurement model and from the measurement parameter
The incident angle for the observation was varied by \(1^\circ\) increments from \(40^\circ\) to \(70^\circ\)
Besides the space limitation due to the component size
the focus of the measurement was on incident angles closer to Brewster’s angle
a SiO\(_2\) optical flat with a refractive index of 1.45 (\(\theta _B= 55.5^\circ\)) was used
The post-selected azimuth angles \(\varepsilon\) were \(0.5^\circ\)
Measurement of amplified SHEL shift reflected from SiO\(_2\) (\(n = 1.45\)) compared to different model of weak measurement model
red dash line represents first order weak measurement model
solid blue line represents the second order weak measurement
and black circle represents measured shift at each incident angle from 40\(^\circ\) to 70\(^\circ\) (a) azimuth angle 0.5\(^\circ\)
the incident angle (\(\theta _i\)) and the post-selected azimuth angle (\(\varepsilon\))
One of the main proposals of this work is the reconstruction of the two-dimensional surface profile of the object under observation through raster scanning. As shown in Fig. 5
the sample stage is mounted on a motorized \(xy\)stage
and data are acquired by recording the beam shift at every spot in the X and Y directions by moving the stage
the scanning is conducted with overlapping steps smaller than the focused beam diameter
The focused beam waist in this setup is 101 \(\upmu\)m
and the scanning step for all measurements is 50 \(\upmu\)m in both the \(x\) and \(y\) directions
After obtaining the data from all the spots along the raster scanning trajectories
each data point is processed based on the SHEL ellipsometry model to retrieve the physical parameters
followed by the reconstruction of the 2D distribution
Scanning measurement of optics samples (a) MgF\(_2\) (\(n = 1.37\))
Scanning of different parts of optical flat (a) sample, (b) reconstruction of the central area, (c) reconstruction of edge area.
Scanning of the optical flat four quadrant’s edge shows different levels of roughness on the outer edge circle detected by SHEL ellipsometry: (a) Result on 1\(^{st}\) area
the polished surface and unpolished surface exhibit different roughness levels
while the unpolished part has a higher Sa of 1.25 nm
The AFM measurement confirmed the different roughness levels of the front and rear parts
Comparison of polished and unpolished surface from AFM and SHEL ellipsometry (a) AFM of polished surface
certain angle parameters in SHEL ellipsometry play crucial roles that impact amplification and measurement results
yet compensating for angle error is also challenging
Future studies should be made to assess the accuracy
such as correlation analysis between AFM and SHEL ellipsometry across varying known surface roughness levels
as well as utilizing an arbitrary incidence polarization angle for greater flexibility
The demand for subnanometer areal surface inspection is rapidly increasing with the advancement of materials
This proposed instrument offers a simple hardware setup without sample size constraints while enabling nanoscale surface characterization
Although it does not provide direct measurements
its efficiency competes with established existing methods such as AFM and SEM
the inferred surface information can be flexibly modeled to suit different sample types
allowing SHEL ellipsometry to analyze a broad range of materials
This adaptability makes it valuable for diverse applications
from precision glass polishing to metamaterial development
This paper demonstrates the application of the SHEL ellipsometry for areal surface measurement
the confirmation of the model with the experiment shows a good agreement
the influence of the post-selected azimuth angle on the measurement result is evident from the retrieval of the pseudo-refractive index
the scanning SHEL ellipsometry shows the reconstruction of the nanometer feature of observed samples
Comparative measurement of known polished and unpolished surfaces validate SHEL ellipsometry as a novel roughness measurement technique
with roughness equivalent thickness \(d_{EMA}\) representing different levels of roughness
the roughness parameter can be expressed as either a pseudo refractive index or an equivalent roughness thickness
depending on the sample’s known properties
SHEL’s sensitivity to changes in the medium’s refractive index offers a significant advantage for nanoscale surface inspection
with unlimited sample size and the ability to indirectly infer the properties of the illuminated area
SHEL ellipsometry enables rapid assessment over large area measurements
Validating the absolute measured value of surface roughness from SHEL ellipsometry presents a challenge
much like other nanometer-scale instruments
Future assessment methods could include correlation analysis or the development of calibration procedures and techniques
The data sets generated during the current study are available from the corresponding authors on reasonable request
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This work was supported by Japan Society for the Promotion of Science (JSPS) KAKENHI Grant Numbers JP19H02154 and JP23K22769
conducted the investigations and prepared the original draft of the manuscript
also contributed to supervision and secured funding for the study
provided supervision throughout the project
All authors discussed and approved the manuscript
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DOI: https://doi.org/10.1038/s41598-025-95988-7
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High areal capacity and low-temperature ability are critical for lithium-ion batteries (LIBs)
the practical operation is seriously impeded by the sluggish rates of mass and charge transfer
the active electronic states of TiNb2O7 material is modulated by dopant and O-vacancies for enhanced low-temperature dynamics
Femtosecond laser-based transient absorption spectroscopy is employed to depict carrier dynamics of TiNb2O7
which verifies the localized structure polarization accounting for reduced transport overpotential
At high-mass loading of 10 mg cm−2 and −30 °C
TNO-x@N microflowers exhibit stable cycling performance with 92.9% capacity retention over 250 cycles at 1 C (1.0-3.0 V
a competitive areal capacity of 1.32 mAh cm−2 can be achieved
Such a fundamental understanding of the intrinsic structure-function put forward a rational viewpoint for designing high-areal-capacity batteries in cold regions
exploiting a practical route to enhance the charge-transfer kinetics of micron-sized TiNb2O7 for high-areal-capacity batteries under low temperatures is urgently desired
the Li-storage behavior of the high-mass-loading TixNbyOz-based electrodes below −30 °C has not yet been reported; and also
the correlation between the intrinsic electronic structure and low-temperature properties remains unclear
The diagram reveal the different lithation kinetics mechanisms between TNO and TNO-x@N
sluggish apparent Li+ diffusion rate and poor intrinsic electronic conductivity are obstacles for high-energy-density batteries in cold regions
the synergistic effect of N-incorporation and O-vacancies can induce localized structure polarization
and promoting Li+ adsorption at low-temperature conditions
a Schematic diagram of the synthesis process of TNO-x@N
d TEM image of TNO-x@N (the inset demonstrates the 3D image of TNO-x@N by Nano-CT technology)
f Aberration-corrected STEM-HADDF image of the TNO-x@N
g Oxygen defect analysis with ABF image of the TNO-x@N
h Atomic-resolution EDS mappings of the TNO-x@N
j Finite element simulation models of Li+ concentration of solid sphere (I) and microflowers (j) for different lithiation states at the current density of 5 C
I Evolution of Li+ concentration in the solid sphere (k) and microflowers (l)
TNO-x@N shows a distinct EPR signal peaks at g = 2.003
This result strongly proves that the thermal reduction process due to the ammonia annealing treatment leads to the appearance of bulk-phase oxygen vacancies in TNO-x@N in addition to surface vacancies
enabling abundant Li+ storage sites and excellent transport ability in the TNO-x@N sample
the bottom layer (near the current collector) of the solid sphere electrode is not lithiated fully
the microflowers electrode allows for a uniform lithiation state
These simulation results highlight the tremendous ion diffusion and storage capability in the compact nanostructure
which is expected to achieve superior low-temperature performance
b The dependent relationship of the formation energy of O-vacancy with concentration and position in TNO-x@N structure
c The corresponding ELF plots of TNO-x@N and TNO
e The electronic conductivities of TNO and TNO-x@N
f PDOS values of the O p orbitals of TNO-x@N and TNO
g Interfacial Li+ adsorption energy (the yellow
i The migration energy barriers in the TNO
the electrical conductivity of TNO-x@N is 1.47 × 10–3 S cm−1
nearly 5 orders of magnitude higher than that of TNO (4.29 × 10–8 S cm−1)
As another key evaluation index reflecting the mass transport, Li+ transport pathways (Fig. 3h) and the corresponding diffusion energy barriers (Fig. 3i) are also calculated
It can be seen that the relatively low diffusion barriers of TNO@N manifests the positive role of N-incorporation for Li+ migration
Li+ diffusion energy barriers decrease with the increase in oxygen deficiency in Ti18Nb36N12O114-x
further indicating the beneficial effects of rational O-vacancies in promoting diffusion kinetics
confirm that the synergistic effect of N-incorporation and O-vacancies can induce localized structural polarization
enhance Li+ adsorption and facilitate electron/ion mobility
a Schematic illustration of principles for femtosecond transient absorption spectroscopy
c The pseudo color TA spectra plots of TNO (b) and TNO-x@N (c) measured after excitation at 3.55 eV
The black lines represent the position of positive and negative boundaries of the TA signal
e TA spectra at different time delays between pump and probe pulse of TNO (d) and TNO-x@N (e)
f Comparison of extracted dynamics at 625 nm probe and bi-exponential function fit curve
g The energy-band structure diagram and recombination processes of excited-state carriers in TNO-x@N
h Schematic diagram of polaron hopping between two identical metal ions with potential energy landscapes
The dark and orange dashed curves indicate adiabatic surfaces of TNO and TNO-x@N
Ea and Ea’ represent the polaron hopping activation energy of TNO and TNO-x@N
i Schematic illustration of Li+ migration accompanies with polaron hopping process (the yellow
a lower ∆Epol has a suppressive effect on polaron formation
which is consistent with the increased trend in the time constant τ1 of the polaron formation process inferentially
resulting in almost 5 orders of magnitude higher measured electrical conductivity of TNO-x@N
we believe that electric delocalization plays an important effect on the formation and transport of polarons
and is one of the main reasons that may contribute to the enhanced electric conductivity and reduced Li ion transport barrier
a Cyclability and b rate capability of the three electrodes with the loading mass of about 1.5 mg cm-2
(1 C = 300 mA g−1) c Comparison of rate performance of TNO-x@N-based batteries with previously reported Nb-based electrodes
d Long-term cycling stability of the TNO-x@N electrode with the mass loading of 1.5 mg cm−2 and 10 mg cm−2 after an activation process of 1 cycle at 0.2 C
e Cross-sectional images of the electrodes with mass loading of 1.5 mg cm−2 and 10 mg cm−2
f Cyclability of the TNO-x@N electrode with the mass loading of 10 mg cm−2 operated at 1 C and −30 °C after an activation process of 3 cycles at 0.2 C
g Temperature-dependent areal capacity and discharge capacity of the TNO-x@N electrode operated from 25 °C to −40 °C
h Rate capability and i cyclability of TNO-x@N | |LiNi0.8Co0.1Mn0.1O2 pouch cell at 25 °C after an activation process of 3 cycles at 0.2 C
(1 C = 250 mA g−1) j Infrared temperature images of TNO-x@N | |LiNi0.8Co0.1Mn0.1O2 pouch cell at 0.5 C and 1.0 C
A high reversible capability of 184.4 mAh g−1 of TNO-x@N after 1000 cycles can be achieved
much better than that of the TNO and solid TNO counterpart
The TNO-x@N electrode exhibits the initial areal capacity of 3.14 mAh cm−2 and 2.36 mAh cm−2 at the current density of 0.1 C
the areal capacity of 2.57 mAh cm−2 and 1.86 mAh cm−2 are obtained
a Cross-section view slice of an original TNO-x@N electrode
b Synchrotron X-ray tomography reconstruction with volume rendering shows the 3D microstructure of the active particles
and pore connectivity network diagram (color indicates local pore center)
d CV curve of half cells at various sweep rates of TNO-x@N at 25 °C
e Capacitive contribution to the total capacity of TNO-x@N with the different mass loading
g The calculated Li+ diffusion coefficients
i Schematic illustration of how TNO-x@N realizes superwettability
and solid TNO with the electrolyte at room temperature
which is highly related with the electron transfer at the solid-liquid interface
the slope angles of the low-frequency region are larger than 45o
implying the existence of capacitive-like behavior during the Li-storage process
Such high capacitive contribution are ascribed to the fast Li-storage at the high working current induced by the synergistic effect between N-incorporation and O-vacancies
the nanosheet-assembled compact structure can provide available extra sites for interfacial storage
which explains why TNO-x@N owns superior rate capability even at low temperatures
and TNO-x@N with the electrolyte at room temperature are 24.3°
further revealing that the TNO-x@N electrode is beneficial for the rapid migration of Li+ between the electrode and the electrolyte
b In situ 2D contour of XRD plots of TNO-x@N (a) and TNO (b)
d Selected 3D surface maps and corresponding contour maps TNO-x@N (c) and TNO (d)
f Lattice-constant variations and corresponding discharge/charge curves of TNO-x@N (e) and TNO (f)
g Nb 3d XPS spectra recorded at different potentials
h–k Ex situ TEM and HRTEM images of the TNO-x@N at the discharge to 1.0 V (h
l Elemental mapping images of the TNO-x@N at the discharged state of 1.0 V
which is attributed to the fact that anion engineering can effectively increase the interlayer spacings
thereby alleviating the repetitive strains induced by the volumetric expansion and contraction during lithiation and delithiation
a charge-transfer-enhanced TiNb2O7-x@N electrode with a unique delocalized electronic structure has been constructed for high-areal-capacity batteries at low temperatures
Time-resolved optical spectroscopy reveals that the heterogeneous adjustment of the electronic structure of TiNb2O7 induces an impurity energy band at the Fermi energy level
lowering polaron hopping activation energy and increasing the free carrier and polaron concentration for improved electronic conductivity
The results are in strong agreement with the theoretical calculations
Such regulation provides an inclination for Li+ adsorption and decreases the energy barriers for ion diffusion
which in turn accelerates electrochemical reaction kinetics
the TNO-x@N electrode exhibits large reversible capacity
It can even deliver an areal capacity of 1.32 mAh cm−2 at −40 °C
a dramatically decreased lattice volume expansion of TNO-x@N electrode is achieved during the lithiated/delithiated process
This work sheds light on the design concept of localized structure polarization
inspiring a pathway of structural engineering strategy toward practical applications of low-temperature batteries
3 mmol niobium pentachloride and 18 mmol oxalic acid were dissolved in 50 mL distilled water and labeled as Solution A
1.5 mmol tetrabutyl titanate and 6 mmol oxalic acid were further dispersed in 20 mL anhydrous ethanol and labeled as Solution B
Solution A was dropped into Solution B to form Solution C
12 mmol ammonium fluoride was added into Solution C by stirring for 100 min to a transparent solution
Solution C was transferred into a 100 mL Teflon-lined autoclave and heated at 180 °C for 12 h
the product was washed repeatedly with alcohol before drying it at 80 °C for 10 h to achieve TNO precursor
The TNO precursor was annealed at 750 °C for 4 h with a heating rate of 5 °C min-1 in a tube furnace to obtain TNO composite
the obtained TNO powder was heated under a mixed Ar/NH3 atmosphere to 700 °C for 1 h to obtain nitrided TNO microflowers (abbreviated as TNO-x@N)
The solid TNO material was obtained by homogeneous mixing of Nb2O5 and TiO2 with a certain ratio in an ethanol solution
followed by heating in a muffle furnace at 1225 °C for 20 h
Crystal structures of samples were investigated by X-ray diffraction (XRD
Bruker D8 Advance) and Raman spectra (Jobin-Yvon Lab RAM HR-800)
Surface chemistry was analyzed with X-ray photoelectron spectra using the PHI 5700-ECSA system
Helios Nanolab 600i) and transmission electron microscopy (TEM
FEI Talos 200 S) were employed to determine the structure and morphologies of the samples
The high-angle annular-dark-field and annular-bright-field images were performed with a spherical-aberration-corrected scanning transmission electron microscope (Titan Cubed Themis G2 300)
Contact angles were acquired on a Cam-plus Micro meter using the sessile-drop technique
and polyvinylidene fluoride (PVDF) was 8:1:1 to fabricate the regular working electrode slurry
which was coated on Cu foils and dried in a vacuum at 100 °C for 10 h
The average loading of active materials in the regular anode was about 1.5 mg cm-2
and the 1C-rate was defined as 300 mA g-1 at the voltage range of 1.0-3.0 V
The electrolyte was a mixture of ethyl carbonate
diethyl carbonate and dimethyl carbonate with a volume ratio of 1:1:1 containing 1 mol L−1 LiPF6
The diameter of the regular electrode was 14 mm
and the diameter of the separator was 16.5 mm
The separator of all half-cells and pouch cells is the Celgard 2500 polypropylene membrane
dimensions and capacity of Li foils were 15.6 mm
and PVDF were homogeneously mixed with a mass ratio of 9:0.5:0.5
The diameter of the high-loading electrode was 12 or 10 mm
the 1C-rate was defined as 250 mA g-1 at the voltage range of 1.0–3.0 V
Lithium metal and LiNi0.8Co0.1Mn0.1O2 were used as electrode materials to assemble half-cells and pouch cell
the slurries consisting of LiNi0.8Co0.1Mn0.1O2 as the active materials
Kejten black & carbon nanotube as the conducting agent
and polyvinylidene fluoride (PVDF) binder in a weight ratio of 95.2:3:1.8 were prepared
The cathode electrode had a mass loading of approximately 6.4 mg cm-2 and a compaction density of 3.45 g cm-3
the pastes consisting of TNO-x@N as the active materials
and PVDF binder in a weight ratio of 92:5:3 were fabricated
The anode electrode had a mass loading of approximately 4.8 mg cm-2 and a compaction density of 2.30 g cm-3
The dimensions of the electrode are 4.3 × 4.2 cm
The N/P ratio of the pouch cell was set to 1.0
the average mass loading of the single-sided anode and cathode electrodes was about 15.4 and 16.1 mg cm-2
The dimensions of the electrode are 4.6 × 8.0 cm
and the cathode and anode electrodes were assembled by stacking the pieces
The 1C-rate is defined as 3.5 A at the voltage range of 1.0–3.0 V
The mass energy density of TNO-x@N-based pouch cell can be quantified by the equation of mass energy density = cell capacity × average voltage/electrode weight
The volumetric energy density of TNO-x@N-based pouch cell can be calculated by the equation of volumetric energy density = cell capacity × average voltage/electrode (thickness × width × length)
Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) were performed on a CHI760 electrochemical workstation
The galvanostatic charge/discharge tests were conducted on the Neware-CT3008 system
According to Fick’s second law of diffusion
TNO and solid TNO electrodes can be computed by:
∆ES and ∆Eτ stand for the change in the steady-state potential and the change in potential after the pulse
The implement of electrochemical simulation was carried out on the surface of the solid sphere and microflowers electrode using the cubic current distribution physical field interface in the COMSOL Multiphsics software
The model is based on the calculation of currents in the electrolyte and electrodes using the “cubic current distribution” interface
the electrolyte current is resolved according to Ohm’s law
and the other is set to the battery potential to meet the total current condition
the electric field follows the continuity equation using the current density:
where \(i\) is the current density vector; zi is the ion charge; mi is the mobility
and ci represents the concentration of the ion
it is consistent with the conservation of current density
Expressions of the Butler-Volmer form are utilized in the simulations to describe the electrode kinetics occurring at the electrode surface inserted in the electrolyte
and the exchange current density for the oxidation reaction is considered to be concentration-dependent
The electrode surface current density is referred to as the Butler-Volmer equation:
The initial value of the electrolyte potential is set to be comparable to the potential of the cell at an open circuit (the open circuit voltage)
ϕl is the electrolyte potential and Eeq is the equilibrium potential
The transport of dissolved Li+ in the electrolyte and electrode during charging and discharging is modeled by transient simulations of the “rare-mass transfer” interface
which assumes that the transport of ions can be described by diffusion according to Fick’s law
mass transfer induced by the diffusion and migration is considered
in which \(c\) represents the concentration of the ions
\({{\mbox{F}}}\) and ϕl stand for the Faraday’s constant and ionic potential
The ionic concentration in the electrode material meets the depletion reaction process
which is modeled using the PDE module of the software:
where ks is the rate of consumption reaction
we set the bottom reference potential as zero potential
and the top as the average current density boundary 2.5 mA/cm2
the conductivity of the electrolyte is set as 4.5 S/m
The diffusion coefficient of the ions as 5 × 10-10 m2/s
and the environmental concentration of the Li ions boundary as 1 mol/L
The femtosecond transient absorption (fs-TA) setup is based on a regenerative amplified Ti: sapphire laser system from a Coherent and Helios pump-probe system (Ultrafast Systems)
The regenerative amplified Ti: sapphire laser system (Legend Elite-1K-HE
and 1 kHz) was seeded with a mode-locked Ti: sapphire laser system (Vitara) and pumped with a Nd: YLF laser (Evolution 30)
the 800 nm output pulse from the regenerative amplifier was split into two parts with a 50% beam splitter
The transmitted part was used to pump a TOPAS Optical Parametric Amplifier (OPA) which generates a wavelength-tunable laser pulse of 350 nm as a pump beam and is chopped by a mechanical chopper operating at a frequency of 500 Hz
Another reflected part of the fundamental beam was introduced into the TA spectrometer to generate the probe light
After passing through a motorized optical delay line
the fundamental beam was focused on a sapphire crystal
which was used to generate the white-light continuum (WLC) probe pulses with wavelengths of 430–820 nm
The optical path difference between the pump light and the probe light
which is controlled by the motorized optical delay line
was used to monitor the transient states at different pump-probe delays
A reference beam was split from the WLC to correct the pulse-to-pulse fluctuation of the WLC
The pump was spatially and temporally overlapped with the probe beam on the sample
two samples of TNO and TNO-x@N were prepared by following steps
TNO and TNO-x@N were added to ethanol in the weight ratio of 10:1 (ethanol: TNO/TNO-x@N)
through ultrasonic dispersion in a water bath for 2 hour
to obtain the TNO and TNO-x@N mixture suspension
the TNO and TNO-x@N films were deposited on cleaned SiO2 substrates by spin coating at 1200 rpm for 30 s
they were sealed with thin SiO2 substrates and epoxy resin to isolate the air
All these steps were conducted in a nitrogen environment at room temperature
in situ cells were assembled in glovebox with Li metal as counter electrode
and 1 mol L−1 LiPF6 in a mixture of the ethyl carbonate
diethyl carbonate and dimethyl carbonate (1:1:1 volume ratio) as the electrolyte
Each XRD curve is collected with a time frame of around 15 min
and the total time for the first cycle of charge and discharge at the current density of 0.25 C is approximately 7.2 h
the coin cells were transferred to a glove box after a certain number of cycles
and dismantled to remove the test electrodes
The removed electrodes were soaked in dimethyl carbonate solution for 12 h and dried and sealed in a glass bottle for subsequent testing
This process always avoids contact with air
The Vienna Ab Initio Simulation Package (VASP) for all the spin-polarized DFT calculations within the generalized gradient approximation (GGA) using the PBE functional formulation was implemented
Projected augmented wave (PAW) pseudopotentials were employed to describe the electron-ion interaction
The valence electronic states were expanded in plane wave basis sets with the energy cutoff of 450 eV
The electronic energy is considered self-consistent when the energy change is smaller than 10−6 eV
while a force change smaller than 0.03 eV/Å is used to determine the convergence of the geometry optimization
Oxygen vacancy formation and lithium-ion migration were calculated using the TiNb2O7 supercell bulk model of 1 × 3 × 1
while the adsorption/desorption of EC-Li was calculated using the TiNb2O7 (001) slab model with a p(1 × 3) supercell
The climbing-image nudged elastic band (CI-NEB) method was applied to obtain the diffusion barriers
The data that support the plots within this paper and other findings of this study are available from the corresponding author upon request. Source data are provided in this paper
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This work was supported by the National Key Research and Development Program of China (2022YFE0138900
the National Natural Science Foundation of China (Grant No
the Shanghai Aerospace Science and Technology Innovation Fund (No
the Young Elite Scientist Sponsorship Program by CAST (No
and the Fundamental Research Funds for the Central Universities (Grant No
Biao Deng of the beamline BL13W1 and BL18B at Shanghai Synchrotron Radiation Facility (SSRF) for SR-CT measurements
These authors contributed equally: Yan Zhang
State Key Laboratory of Space Power-Sources
conceived the project and designed the experiments
contributed to part of the preparation and characterization of the material and the electrode
wrote the manuscript with support from all authors
Nature Communications thanks the anonymous reviewers for their contribution to the peer review of this work
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DOI: https://doi.org/10.1038/s41467-024-50455-1
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Empathy enables understanding and sharing of others’ feelings
Human neuroimaging studies have identified critical brain regions supporting empathy for pain
the precise spatio-temporal profiles of empathic neural responses and inter-regional communications remain elusive
we investigated electrophysiological signatures of vicarious pain perception
Others’ pain perception induced early increases in high-gamma activity in IFG
but decreased beta power in AI and amygdala
Vicarious pain perception also altered the beta-band-coordinated coupling between ACC
as well as increased modulation of IFG high-gamma amplitudes by beta phases of amygdala/AI/ACC
We identified a necessary combination of neural features for decoding vicarious pain perception
These spatio-temporally specific regional activities and inter-regional interactions within the empathy network suggest a neurodynamic model of human pain empathy
it is crucial to assess the spatio-temporal dynamics of neural oscillations and inter-regional communication modes in empathy-related regions to understand how functionally diverse processes dynamically merge into empathic responses towards others’ feelings
(i) the temporal order and spectral patterns of neural activity in different empathy-related brain regions
(ii) the rapid functional interactions between different brain regions remains elusive
(iii) it is also unclear whether and how vicarious pain perception can be decoded from multiple features of the neural activity and inter-regional communications
The current study aimed to address these questions by recording intracranial electroencephalography (iEEG) signals during the perception of others’ pain
This helps us understand how the brain gives rise to empathic responses to vicarious pain
reveal the dynamic organization of the empathy network
and construct a neurodynamic model of empathy
these studies focused exclusively on a single empathy-related region
it remains elusive how the anatomically distributed and functionally distinct neural activity within the empathy network are temporally and spatially organized during perception of others’ pain
The current study sought to reveal the region-specific spectral patterns and the temporal order of empathic neural responses by recording neuronal population activities in four key empathy-related nodes—the ACC
and IFG—in 22 epilepsy patients while they viewed pictures depicting painful stimulation applied to others’ hands
Thus we examined both low-frequency coupling and phase-amplitude coupling to assess how the ACC
and IFG interacted when observing other’s suffering
Leveraging the strengths of iEEG and advanced analysis of neurophysiological signals
we provided a spectral-temporal-spatial map of neuronal population activity and inter-regional interaction dynamics that subserved empathic pain experience in humans
In an effort to delineate the specific contributions of these spectral-temporal-spatial specific patterns to vicarious pain perception and identify important neural features
we further investigated how these neural features jointly contributed to the perception of others’ pain
to assess the associations between empathic responses and critical neural features within the pain empathy network
we tested how these critical neural features were linked to empathy-related behavioral measures
including the strength of overall empathic responses and empathy-related subprocesses (i.e.
evaluation of perceived pain intensity and one’s own unpleasantness) during perception of other’s pain
This investigation was potentially important for empathy research as it would help assess the importance of different types of neural features for vicarious pain perception and identify tailored targets for interventions of empathy-related deficits
providing evidence for empathic responses to other’s pain in our patients
patient and healthy individuals showed similar response patterns in differentiating painful and non-painful stimuli
patients’ empathic responses to vicarious pain were comparable with those of healthy individuals
showing evidence for early and sustained involvement of high-gamma IFG activity in the processing of vicarious pain
we calculated power correlations in the overlapping frequency bands of the respective intra-regional power effects for each pair of regions (alpha and beta bands for ACC-AI; beta band for ACC-amygdala and AI-amygdala)
power correlation was computed as the Fisher-z-transformed correlation coefficient across the stimulus-presentation window (i.e.
We then compared the power correlation coefficients between painful and non-painful conditions (two-tailed paired t-tests for each frequency
using cluster-based permutation tests to correct for multiple comparisons)
from AI to amygdala and from the amygdala to AI) across the stimulus-presentation time window
We averaged TE values across frequency ranges of the corresponding power correlation effect and submitted them to repeated-measures analyses of variance (ANOVAs) with Pain (painful vs
non-painful stimuli) and Direction as within-subjects factors
For the interactions between the ACC and amygdala at 25–30 Hz
no significant results were found for the main effect of pain or the interaction effect (Main effect of pain: F1
We thus tested whether the phase of low-frequency oscillations in the AI/ACC/amygdala modulated high-gamma amplitudes of the IFG during empathic responses by performing inter-regional phase-amplitude coupling (PAC) analysis
The phase and amplitude time series were obtained for frequencies in the frequency bands of the respective intra-regional power effect (phase frequency bands: alpha/beta bands in the ACC
and beta band in the amygdala; amplitude frequency: 70–150 Hz in the IFG)
PAC values were indexed by circular-linear correlation coefficients between the phase time series and the amplitude time series
We then compared the Fisher-z-transformed PAC values across channel pairs between the painful and non-painful conditions (two-tailed paired t-tests for each frequency pair
We tested how the neural activity and neural synchronization in the ACC
and IFG contributed to the detection of other’s pain
we employed a support vector machine to construct a decoder to discriminate perception of painful and non-painful stimuli from power
we split our dataset into two parts at the channel or channel-pair levels (detailed in Methods)
One feature-selection dataset where we performed time-frequency decomposition of iEEG signals for each region and calculated inter-regional correlations of low-frequency power and PAC value for channel pairs
was used to select relevant features (see Methods)
The other decoding dataset was used to construct and validate the classification model
As a validity check of our classification model before further analyses
we assessed its classification performance and found that our classification model significantly differentiated labels of painful and non-painful stimuli (classification accuracy = 76.28%
indicating that this eight-feature combination is necessary for discriminating between painful and non-painful stimuli
the removal of this eight-feature combination led to significantly lower decoding accuracy compared to randomly removing an equal number of features (p < 0.001)
further supporting the importance of this eight-feature combination in vicarious pain perception
This suggested that stronger empathic responses were linked to greater suppression of ACC alpha oscillations and AI low-frequency oscillations
These findings further suggested that suppressed ACC alpha power and AI low-frequency power not only facilitated qualitative differentiation between others’ pain and non-pain (signaling the presence of other’s pain) but also quantitatively tracked the strength of empathic responses
These results showed that stronger suppression of AI low-frequency power was related to higher intensity of perceived pain in others but a lower level of self-related unpleasantness
the observed neural effects cannot be attributed to potential differences in arousal levels between painful and non-painful stimuli
Our iEEG results revealed the precise spectro-temporal characteristics of neural responses in the key regions of the empathy network (i.e.
and IFG) and the electrophysiological basis of the inter-regional communications among these regions during perception of others’ pain
The oscillatory patterns and inter-regional functional interactions provide insights into our understanding of how different processes dynamically coordinate and merge into empathy for pain
It would be valuable for future research to directly test this possibility
it remains unclear how rapid communications between empathy-relevant brain regions support empathic responses in humans
Our iEEG results provided electrophysiological evidence for the engagement of these two circuits in human empathy
suggesting the ACC/AI-amygdala circuit as an evolutionarily conserved mechanism of empathy
we identified a different mode of inter-regional communication related to empathy — cross-frequency coupling between high-gamma IFG and beta ACC/AI/amygdala — which points towards new directions for future investigations into empathy-related circuits
The current study provided evidence for both increased functional interactions (e.g.
enhanced coupling between ACC beta phase and IFG gamma amplitude) and decreased inter-regional communications (e.g.
attenuated beta coupling between ACC and AI) within the empathy network
These patterns highlighted rapid information flow among different brain regions to coordinate diverse processes of empathy
the brain needs to not only enhance functional interactions between specific empathy-related regions (e.g.
potentially facilitating their coordination and information integration but also appropriately suppress certain inter-regional communications in order to reduce mutual distractions and increase functional specialization of relevant brain regions (e.g.
These findings on empathy-related inter-regional communication aid in understanding how the brain generates empathic responses towards others’ pain
The behavioral and neural data in the current work were collected from epilepsy patients
the disease or treatments might impact our findings to a minimum extent
Patients in our study indeed perceived others in stronger pain
and reported stronger empathic responses when seeing others in painful (relative to non-painful) situations
patients and healthy controls showed comparable behavioral performances during judgments of others’ pain and subjective ratings of each stimulus
patients’ neural responses were predictive of the strength of empathic responses
as well as their own ratings of perceived pain intensity and unpleasant feelings of vicarious pain
These results provide consistent evidence for the engagement of empathic response to painful stimuli in patients and the behavioral and neural patterns observed here reflect response profiles of perceived pain in others
It would be interesting for future studies with larger sample size and trial number to further investigate if and how the experimental task modulates spectral patterns within different subregions of the insula as well as other empathy-related regions during processing others’ pain
our iEEG results revealed frequency-specific patterns in the key nodes of the empathy network and identified two inter-regional communication modes as crucial neurophysiological mechanisms underlying empathy for pain
our findings of the beta-band-coordinated synchronization between the AI
as well as the cross-frequency coupling between the AI/ACC/amygdala (low-frequency) and IFG (high-gamma)
provide insights into how functionally diverse and spatially distributed brain regions communicate and coordinate when perceiving others in pain
These findings contribute to a sophisticated understanding of the neural dynamics of empathy
which may help with the prediction of empathy-motivated prosocial behaviors and the development of therapeutic interventions targeting empathy-related deficits commonly observed across various neuropsychiatric disorders
electrode localizations were exclusively determined by clinical needs
We prioritized and maintained the integrity of clinical care during conducting the current study
All patients provided informed consent after the experimental procedure had been fully explained
and were acknowledged their right to withdraw at any time during the study
The experimental design and procedures adhered to the standards set by the Declaration of Helsinki and were approved by the local Institutional Review Board of each hospital where the patients were tested (i.e.
the Chinese PLA General Hospital: S2021-394-02
Beijing Xuanwu Hospital: ClinRes No.2022018
and Beijing Tiantan Hospital: KY 2020-080-02)
Data were recorded from 29 epilepsy patients who were implanted with intracranial depth electrodes and were undergoing intracranial EEG monitoring to localize the seizure onset zone for potential surgical resection
All participants recruited in the current study had no history of psychiatric disorders
Patients did not take pain medication several hours prior to the iEEG recording of the pain judgment task and were not experiencing any physical pain during the iEEG recording
The patient selection was based on two inclusion criteria: (i) having electrodes in the ACC
or IFG contralateral to or outside of the epileptogenic zone; and (ii) achieving a response accuracy above 50% in the pain judgment task
one patient was excluded due to a low response accuracy (45%) in the pain judgment task
and six patients were excluded because no electrodes were implanted in the regions of interest
The remaining 22 patients were included in the behavioral and neural analysis of the pain judgment task (13 males
alpha error = 5%) confirmed that we had sufficient power (86.94%) to detect medium effect sizes (d = 0.5) even with the minimum number of channels (n = 40)
We employed stringent thresholds and the main findings are highly significant statistically
and survived correction for multiple comparisons
and color of the painful and non-painful stimuli were matched
Each stimulus was presented on a gray background of a 21.5-inch color monitor during iEEG recording
subtending a visual angle of 11.33° × 8.51° at a viewing distance of 80 cm
Participants were then presented with a painful or non-painful picture with a duration of 500 ms and were instructed to understand and empathize with the emotional states of the person depicted in the pictures
To motivate and monitor engagement in the task
participants were asked to indicate whether the person in each picture experienced pain or not (as specified by Chinese instruction: “请您判断图片中的人是否感到疼痛”) by pressing the left (index finger) or right (middle finger) button using their dominant hands after the picture disappeared
Participants made these responses on a self-paced basis and were encouraged to respond as accurately as possible
the picture viewing phase and response phase were separated in order to isolate vicarious pain perception from any potential biasing effects of motor responses on neural responses to others’ pain
painful and non-painful pictures were presented once in a random order
These results suggested that the observed neural effects were not due to potential differences in arousal levels between painful and non-painful stimuli
To demonstrate that patients were not impaired in their responses to vicarious pain
and showed empathy-related behavioral patterns similar to that in healthy controls
we recruited a healthy participant sample whose gender and age distributions were comparable to those of the patient sample (n = 22; 9 males
age = 23.18 ± 2.38 years old) (age: t42 = −0.81
two-sided two-sample t-test; gender: χ2(1) = 0.82
two-sided Pearson’s Chi-square test of independence)
Healthy participants were asked to complete the same pain judgment tasks and provide subjective ratings of the strength of empathic response
and their own unpleasantness for each stimulus
We then compared subjective ratings between painful and non-painful stimuli to check empathic responses to others’ pain in our patients (two-tailed paired t-tests)
We then examined whether patients and healthy participants showed different responses and subjective feelings to vicarious pain
Data were averaged across trials in each condition for the response accuracy and time in the pain judgment task and subjective ratings
we examined group differences between patients and healthy participants by constructing linear mixed-effect models with participants as a random effect to control for individual variations
the aggregated data were then entered into separate linear mixed-effect models to compare between two groups
which included fixed-effects of pain (painful vs
We then performed F-tests on the fixed effects estimates (two-tailed)
The null distribution was generated by randomly flipping the sign of Fisher-z-transformed patient-normative correlations or healthy-normative correlations
we examined the difference between the patient-normative and healthy-normative correlation coefficients (two-tailed permutation tests) by creating a null distribution via randomly shuffling membership between patient group and the healthy participant group
iEEG data were recorded using amplifiers from a Nicolet electroencephalogram system (256 channel amplifier
the Chinese PLA General Hospital) or a Nihon Koheden system (256 channel amplifier
or a Micromed system (128 channel amplifier
Each electrode was 0.8 mm in diameter and contained 5 to 18 contact leads 2 mm wide and 1.5 mm apart
iEEG data for the pain judgment task were collected when no subclinical or clinical seizures occurred during or immediately before the task
All the remaining channels were also visually inspected to ensure that all bad channels had been removed
we visually screened all channels for epileptic charges and removed those with too many remaining artifacts
All visual inspections were performed while blinded to the experimental conditions
and then conducted paired-t tests to examine the conditional power differences among the random channels
This procedure was repeated for 1000 times
resulting in 1000 t values to construct the null distribution
The observed conditional power difference was then compared with this null distribution
We found that the observed conditional effects of all these clusters were significantly stronger than those calculated based on random channels (ACC alpha cluster: p = 0.011
ACC beta cluster: p < 0.001; AI low-frequency cluster: p < 0.001; amygdala beta cluster: p < 0.001; IFG high-gamma cluster: p < 0.001)
we investigated the power correlations between each region pair of the AI
and amygdala in overlapping frequency bands that significantly differentiated between painful and non-painful stimuli (including the alpha and beta bands for ACC-AI and the beta band for ACC-amygdala and AI-amygdala)
To eliminate the potential influence of individual differences
we only considered pairs of channels within each participant (i.e.
the two channels of each pair from the same participant) and included participants with at least one channel pair
the inter-regional PAC values were computed as the circular-linear correlation coefficient between the phase time series of the amygdala/AI/ACC and the amplitude time series of the IFG (across the post-stimulus time window
0–500 ms) and Fisher-z-transformed and averaged across all epochs in each condition
we performed feature selection and model construction using separate datasets
we randomly split our data into two independent sub-datasets at the channel (or channel pair) level
with 70% of the data as the feature-selection dataset to identify informative features
and the remaining 30% of the data as the decoding dataset to construct the classification model to decode stimulus types
we linearly scaled each feature to the range [0
the classification performance of the SVM classifier was evaluated by a five-fold cross-validation procedure
We randomly divided all trials into 5 folds
the classifier was trained on the remaining 4 folds and then tested on the held-out testing fold
The decoding accuracy of the confusion matrix (i.e.
(true positive + true negative)/total observation) was calculated based on the average of five iterations
we calculated the average accuracy across all iterations and resamples as a result
We assessed the statistical significance of the decoding accuracy using a permutation test104
we randomly shuffled the class labels and the entire decoding procedure detailed above was repeated
we obtained the null distribution of decoding accuracy
which can well-capture the variability of decoding accuracy corresponding to the current sample size
We controlled for the influence of limited sample size on the variations of decoding accuracy by comparing the true decoding accuracy with this null distribution (one-tailed
the operations to respectively remove each feature from the model resembled the scenarios when a specific feature was disrupted
As none of the neural features can individually determine the success of the decoding
we further searched for feature combinations which were necessary for successful decoding
We performed stepwise classification by removing features sequentially and evaluating the classification performance of the remaining features until the decoding accuracy was reduced to the chance level
Those removed features consisted of a necessary feature combination for successful decoding
To lend further evidence to strengthen the importance of the detected feature combination
we took into account the influence of feature numbers and compared the decoding accuracy when removing this feature combination to that when randomly removing an equal number of features (random removing for 1000 times
For each feature encoding empathic strength
we conducted similar analyses to explore whether and how this feature was associated with perceived pain intensity in others and one’s own unpleasantness when witnessing others in pain
All the independent and dependent variables were standardized before entering in the model and all the two-tailed p-thresholds were adjusted via FDR-correction based on the number of statistical tests
Given the limited number of patients who completed post-iEEG ratings
we applied a less stringent threshold of FDR corrected p < 0.05 for all these analyses to reduce risk of false negatives
we also checked the associations between the neural features encoding empathy strength and arousal ratings to further demonstrate their specificity in the encoding of empathy-related behavioral responses
Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article
The raw and preprocessed iEEG data generated in this study have been deposited in a local database. The iEEG data are available under restricted access as they contain personally identifiable information and patients have not consented to data distribution. Access can be obtained from the corresponding author upon request. Source data are provided with this paper
The code to perform wavelet transform and compute power correlations and phase-amplitude coupling is publicly available (https://github.com/Huixin-Tan/iEEG_empathy)
The access of other codes is available from the corresponding author upon request
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Yuan for their assistance in data collection
This work was supported by the National Natural Science Foundation of China (Projects 32125019 to Y.M.; 32230043 to S.H.); STI 2030—Major Projects 2022ZD0211000 to Y.M.; the Fundamental Research Funds for the Central Universities (2233300002 to Y.M.); and the start-up funding from the State Key Laboratory of Cognitive Neuroscience and Learning
State Key Laboratory of Cognitive Neuroscience and Learning Beijing Normal University
Beijing Key Laboratory of Brain Imaging and Connectomics
School of Psychological and Cognitive Sciences
PKU-IDG/McGovern Institute for Brain Research
conceived of the project and designed the experiments; X.Z.
and F.M performed the experiments and collected data; H.T.
analyzed the data under the supervision of Y.M.; H.T
All authors approved the final version of the manuscript for submission
Nature Communications thanks Efe Soyman and the other
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DOI: https://doi.org/10.1038/s41467-024-49541-1
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Volume 8 - 2020 | https://doi.org/10.3389/feart.2020.607049
Geomagnetic jerks are sudden changes in the geomagnetic field secular variation related to changes in outer core flow patterns
Finding geophysical phenomena related to geomagnetic jerks provides a vital contribution to better understand the geomagnetic field behavior
we link the geomagnetic jerks occurrence with one of the most relevant features of the geomagnetic field nowadays
which is due to the presence of reversed flux patches (RFPs) at the Core-Mantle Boundary (CMB)
Our results show that minima of acceleration of the areal extent of SAA calculated using the CHAOS-7 model (CHAOS-7.2 release) coincide with the occurrence of geomagnetic jerks for the last 2 decades
a new pulse in the secular acceleration of the radial component of the geomagnetic field has been observed at the CMB
with a maximum in 2016.2 and a minimum in 2017.5
along with the minimum observed in 2017.8 in the acceleration of the areal extent of SAA
We have also analyzed the acceleration of the areal extent of South American and African RFPs at the CMB related to the presence of the SAA at surface and have registered minima in the same periods when they are observed in the SAA at surface
This reinforces the link found and would indicate that physical processes that produce the RFPs
contribute to the core dynamics at the origin of jerks
The secular variation of the core geomagnetic field is generally characterized by smooth variations in time. However, since the end of the 1970s with the works of Courtillot et al. (1978) and Malin et al. (1983), the geomagnetic community has been interested in the occurrence of abrupt changes, not globally simultaneous (Brown et al., 2013)
observed in the trend of the first derivative of the field elements
They used between six and four geomagnetic observatories to estimate the occurrence times of the most recent geomagnetic jerks
they found alternated sign of the acceleration at some regions that
when associated with large spatial scale structures
could cause geomagnetic jerks at the Earth’s surface
By using global geomagnetic field models based on paleomagnetic data, Terra-Nova et al. (2016) observed that the reversed flux patches (RFPs) present at the CMB
regions with an opposite polarity to that expected for an axial dipole
were mostly located in the Southern Hemisphere
especially in the South Atlantic and Indian regions
FIGURE 1. Geomagnetic field on January 1, 2020. (A) Intensity at the surface and (B) radial component (Br) of the geomagnetic field at the CMB on January 1, 2020, from CHAOS-7.2 model (Finlay et al., 2020). The white line in (A) marks the contour line of 32,000 nT to highlight the area of the SAA defined following De Santis et al. (2012)
In (B) the two RFPs related to the presence of the SAA at the surface are observed in red colors in the Southern Hemisphere
We use CHAOS-7.2 model until degree 13 to calculate the intensity at the surface and until degree six for Br at the CMB
In the search for understanding geomagnetic jerks, an important element is to investigate possible correlations between these events and some other geophysical phenomena (see Mandea et al., 2010 for a review on some of the up-to-date suggested links)
we suggest that the minima of the acceleration of the areal extent of SAA could be a reliable indicator of the occurrence of geomagnetic jerks
being able to register all of the well-defined geomagnetic jerks for the last 2 decades
and then provide a discussion about the dynamic processes at the CMB that could be involved in this link and the possible identification of future geomagnetic jerks occurrence from this result
This study has been carried out using the CHAOS-7.2 model, the release of the CHAOS-7 model (Finlay et al., 2020) that uses the Swarm preliminary baseline 0603 data up to the end of March 2020 and ground observatory data as available in February 2020. The Swarm satellite mission (Olsen and Haagmans, 2006 and references therein) was launched by ESA in November 2013
based on a constellation of three identical satellites (Alpha
provides high quality measurements of the geomagnetic field in three different orbital planes
with Alpha and Charlie flying almost in parallel and Bravo orbiting alone at a higher altitude
along with those given by other previous satellite missions (Cryosat-2
and Ørsted) and the global network of magnetic observatories at ground level
provide the possibility of obtaining high-resolution time-dependent geomagnetic field models such as the CHAOS-7 model and later releases
we use the finite differences between successive times
with ti+1/2 = ti + 3 months and ti+1 = ti + 6 months
and (C) second derivative S ̈ of the areal extent of the SAA for the last 2 decades calculated from CHAOS-7.2 model monthly from January 1998 to March 2020
The fit of the areal extent of the SAA by using cubic splines is plotted in orange in (A)
the mean occurrence times of the well-defined geomagnetic jerks for the last 2 decades are marked
Shaded bands mark the uncertainty of the occurrence times given by one standard deviation
With green arrows some interesting features are indicated (see Discussion in the main text for more details)
For the second derivative, S⋅⋅, we use the finite differences method of second order following Tozzi et al. (2009)
with ti+1 = ti + 6 months and ti−1 = ti−6 months for the same period
Prior to the estimation of these derivatives, we smooth the areal extent of the SAA series by fitting the data using a cubic splines basis with knot points every year from 1998 to 2020.2 in order to avoid subsequent mathematical artifacts from the derivatives (orange line in Figure 2A)
As expected, the S˙ values are positive (Figure 2B); that is, the areal extent of the SAA is increasing in the analyzed time interval with an average rate of 4.4 ∙ 105 km2/yr. In Figure 2C it is observed that this increase of the SAA is not continuously accelerated (see also Pavón-Carrasco and De Santis, 2016)
alternating periods of accelerations (beginning –1999.0
and 2017.8–2019.6) and decelerations (1999.0–1999.9
The time intervals when the S⋅⋅ reaches positive values (2000.7–2001.1
2014.8– end) are characterized by longer displacements of the areal extent of the SAA
These intervals present a duration from 1 to 3 years
being the longest period of positive S⋅⋅
the maximum increase of areal extent of the SAA for the last 2 decades
the longest period with positive S⋅⋅ would be from 2014.8 up to now
but this result must be considered carefully because it could be affected by edge problems of the CHAOS-7.2 model
These edge problems could also be present at the beginning of the model
the borders being the periods most subject to change
in the minima of S⋅⋅ (1999.9
and 2017.8) the areal extent of the SAA is slowing down its advancement
- The 1999 geomagnetic jerk occurrence time: occurrence dates of the 1999 geomagnetic jerk were given in Supplementary Table A4 by Pinheiro et al. (2011). They are 54 occurrence dates calculated from the annual means of the geomagnetic components X, Y, and Z in 42 observatories. The mean (and standard deviation) of these 54 occurrence dates provides the value of 1999.0 (±0.9) plotted in Figure 2C
- The 2003 geomagnetic jerk occurrence time: the 2003 geomagnetic jerk is identified by a relative peak in number of global jerk identifications between 2002 and 2003 (see Figure 15 in Brown et al., 2013). This interval can be rewritten as 2002.5 (±0.5) and plotted in Figure 2C
It is important to note that these observatories are not evenly distributed geographically
More space and time extended studies of magnetic observatories could result in more accurate estimations of the occurrence times of these jerks
As we can observe, the minima of the acceleration (S⋅⋅) of the areal extent of the SAA (Figure 2C) coincide quite well with the geomagnetic jerks occurrence for the last 2 decades
The main differences are found in the earlier times but within the uncertainty shown by shaded bands
where the edge effects could be more significant by the effect of the smoothing of the splines basis used to represent the temporal variations during the modeling process
Despite some discrepancies mainly due to edge effects
these tests confirm the results obtained with CHAOS-7.2
Secular acceleration of the areal extent of the RFPs at the CMB
Time evolution of the second derivative of the areal extent of the South American (blue line) and African (red line) RFPs and (green line) the sum of both areal extents at the CMB
The areal extent is calculated as the area within the contour line of −32,000 nT of Br (shown in the map in the figure) using CHAOS-7.2 model until degree 6
With green arrows other interesting features are indicated (see Discussion in the main text for more details)
This lack of synchronization between RFPs makes it difficult to provide an accurate estimation of the time occurrence of the minima when both RFPs are considered together
and it reveals the complexity of the mechanisms involved
This means that in the minima of the second derivative of the areal extent of the RFPs
which seem to be associated with the occurrence of the geomagnetic jerks
there is a decrease in the rate of evolution of the areal extent of the RFPs: the African RFP slows down its extent (slow reinforcement of Br) and the South American RFP vanishes slower (slow weakening of Br)
This behavior could be due to a weakening and later reinforcing of the upwelling of toroidal field from the core in the case of the African RFP and vice versa for the South American RFP
This is also observed when the average is calculated on the region where the RFPs associated with the SAA are located
which reinforces the link between SAA and jerks
it is worth to mention that observed SA might be a time average of the true instantaneous SA
especially when using geomagnetic field models with temporal damping
This could be a limitation to correlate on a very accurate way some features of the SA in time
Averaged secular acceleration of the geomagnetic field at the CMB
Time variation of the averaged squared secular acceleration of the Br calculated using maximum spherical harmonic degree six at the CMB
we consider only positive lobes of the SA of Br for average
we consider only negative lobes of the SA of Br
we consider the SA of Br in the region where the RFPs associated with the SAA at surface are located at the CMB (between 20°S and 70°S in latitude and between 90°W and 70°E in longitude)
the analysis of the second derivative of the areal extent of SAA demonstrates to be a promising instrument to identify this kind of poor-defined jerks
Further investigations will be needed in order to confirm these possibilities
Whether the trend of the SAA areal extent does not change, the detection of a relative maximum of S⋅⋅ of the SAA could indicate coming geomagnetic jerks with around 1.5 years in advance, according to Figure 2C. This is within the mean time of 6–7 years after which no reliable prediction for the field can be made following Qamili et al. (2013)
where a longer period of around 5–10 years is also identified
Wavelet analysis with Morlet basis functions of (upper panel) the global averaged squared secular acceleration of the radial component (Br) of the geomagnetic field at the CMB
(middle panel) second derivative (acceleration) of the areal extent of the South American and African RFPs
and (bottom panel) the second derivative (acceleration) of the areal extent of SAA for the last 2 decades
The shaded plot indicates the nonsignificant part of the analysis and the black lines mark the common period found
The relation between geomagnetic jerks and pulses of the global averaged squared SA of the Br at the CMB seems clear from Figure 4 (see also Chulliat et al., 2010; Chulliat and Maus, 2014; Kloss and Finlay, 2019) but also with the SAA (even if with lower amplitudes between 2006 and 2014) as shown by the blue curve of the same figure
This means that possibly the particular core dynamics associated with the SAA
is related to the detection of jerks at surface; that is
the SAA area is a region especially sensitive for the identification of geomagnetic jerks
Chulliat and Maus (2014) carried out a Principal Component Analysis to determine the variability modes (Empirical Orthogonal Functions
EOF) of the SA of the geomagnetic field at the CMB associated with the occurrence of geomagnetic jerks
Three principal modes were obtained: EOF #1 and EOF #2 presented maxima and minima lobes of the SA located in low and middle latitudes of the Atlantic sector (where the SAA is located nowadays); EOF #3 was characterized by maxima and minima of the SA in the Indian sector
Secular acceleration of the Br of the geomagnetic field at the CMB
Maps of the secular acceleration of the Br at CMB for January 1 for every year during the last 2 decades
We use CHAOS-7.2 model until degree six to calculate the Br
this could mean that when the upwelling of toroidal field presents a change associated with a minimum in the second derivative of the areal extent of the RFPs and
We suggest a previously unreported link between the minima of the second derivative of the areal extent of SAA at surface and the occurrence of geomagnetic jerks for the last 2 decades
by studying the areal extent of the RFPs associated with the presence of the SAA at surface
We have seen that global SA pulses at the CMB related to the occurrence of the geomagnetic jerks are also detected locally on the area at the CMB affected by the RFPs associated with the presence of the SAA at surface
We have seen that the areal extent of SAA is able to detect through its relative minima all impulses of the geomagnetic field at surface (and
This fact is of particular interest because it could shed light on geomagnetic jerks identified in some
the occurrence of the 2005.0 geomagnetic jerk is discussed
detected as a minimum of the second derivative of the areal extent of SAA
could be an impulse of the geomagnetic field associated with the asymmetry of the positive and negative lobes of the SA of the geomagnetic field at the CMB
It could be considered as a new kind of impulse of the geomagnetic field but also as a poor-defined jerk
It is also important to take into account that the jerks can be poorly defined particularly when we have to distinguish between successive events in disparate regions of the globe that overlap in time
this work is encouraging because it aims to give links to effects at the CMB that help to simplify the view of the surface expressions
it could be possible that the relation between the arrival of quasi-geostrophic Alfvén waves at the CMB and the presence of nonzonal azimuthal flow accelerations of alternating sign could affect the upwelling of toroidal field present in higher latitudes
When a rapid change of the sign of these flow accelerations is produced
this would coincide with a change of the upwelling regime
observed as a minimum in the second derivative of the areal extent of the RFPs at CMB and of the SAA at surface
This could provide an important hint about the dynamic processes that link the RFPs and
with the geomagnetic jerks at the interior of the Earth
The original contributions presented in the study are included in the article/Supplementary Material
further inquiries can be directed to the corresponding author
SAC developed the project and performed the calculations with the help of FJPC
The interpretation of the results and writing were led by SAC with the help of FJPC
and EQ discussed the results and commented on the manuscript
The Living Planet Fellowship (TEMPO project) from ESA
is the main financial support to this research
ASI Limadou-Science Project has supported this work partially
Grant FPU17/03635 from the Spanish Ministry of Education was funding AGL PhD thesis
FJPC was partially supported by the Spanish research project PGC2018-099103-A-I00
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest
The authors are very grateful to Editor and two reviewers for their useful comments that have helped to improve the quality of this manuscript
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/feart.2020.607049/full#supplementary-material
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González-López A and Qamili E (2021) South Atlantic Anomaly Areal Extent as a Possible Indicator of Geomagnetic Jerks in the Satellite Era
Received: 16 September 2020; Accepted: 27 October 2020;Published: 14 January 2021
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GRINDAVIK, Iceland (AP) — A volcano in southwestern Iceland that has erupted repeatedly for more than a year again belched lava and smoke into the air on Tuesday
just hours after authorities evacuated the few remaining residents of a nearby fishing village
triggering warning sirens in the town of Grindavik where webcams showed molten rock spewing toward the community
Police and civil defense officials evacuated Grindavik and the Blue Lagoon geothermal spa
one of Iceland’s biggest tourist attractions
after an early morning earthquake swarm suggested an eruption was imminent
The community, located on the Reykjanes Peninsula, was largely evacuated in November 2023 when the volcano came to life after lying dormant for some 800 years
though police reported that some residents refused to leave their homes
“Those individuals who choose to remain in the town don't seem to consider that I have 50 people involved in this operation
some of whom are volunteers,” Úlfar Lúðvíksson
“I would ask that more consideration be shown towards civil defense.”
Iceland sits above a volcanic hot spot in the North Atlantic. The most disruptive incident in recent times was the 2010 eruption of the Eyjafjallajokull volcano, which spewed clouds of ash into the atmosphere and disrupted trans-Atlantic air travel for months.
Flights were not affected by Tuesday's eruption.
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Volume 13 - 2019 | https://doi.org/10.3389/fnana.2019.00039
Subplate (SP) neurons are among the earliest-born neurons in the cerebral cortex and heterogeneous in terms of gene expression
SP neurons consist mainly of projection neurons
which begin to extend their axons to specific target areas very early during development
the relationships between axon projection and gene expression patterns of the SP neurons
we analyzed the corticocortical projections of L6b/SP neurons in the mouse cortex and searched for a marker gene expressed in L6b/SP neurons that have ipsilateral inter-areal projections
Retrograde tracing experiments demonstrated that L6b/SP neurons in the primary somatosensory cortex (S1) projected to the primary motor cortex (M1) within the same cortical hemisphere at postnatal day (PD) 2 but did not show any callosal projection
This unilateral projection pattern persisted into adulthood
Our microarray analysis identified the gene encoding a β subunit of voltage-gated potassium channel (Kcnab1) as being expressed in L6b/SP
Double labeling with retrograde tracing and in situ hybridization demonstrated that Kcnab1 was expressed in the unilaterally-projecting neurons in L6b/SP
Embryonic expression was specifically detected in the SP as early as embryonic day (E) 14.5
Double immunostaining experiments revealed different degrees of co-expression of the protein product Kvβ1 with L6b/SP markers Ctgf (88%)
suggesting molecular subdivision of unilaterally-projecting L6b/SP neurons
scattered expression of Kcnab1 was observed during postnatal stages without layer specificity
Among splicing variants with three alternative first exons
the variant 1.1 explained all the cortical expression mentioned in this study
our data suggest that L6b/SP neurons have corticocortical projections and Kcnab1 expression defines a subpopulation of L6b/SP neurons with a unilateral inter-areal projection
expression of SP-specific genes at a critical period during development almost certainly underlies the fine orchestration of SP axon projection pattern and regulates cortical maturation
the relationship between molecular identity and axon projection target specificity remains largely elusive
We found a proportion of L6b/SP neurons that project unilaterally from S1 to M1 can be molecularly identified by a specific splice variant of the voltage-gated potassium channel Kcnab1
This discrete group of neurons was present at different stages of development
although the expression pattern of Kcnab1 changed as the brain matured
There was also a considerable overlap between the Kvβ1-positive neurons in L6b/SP with known L6b/SP molecular markers
our results suggested that this molecularly distinctive group of neurons is most likely a L6b/SP subpopulation that survives as the cortex develops and may underlie inter-areal circuit establishment in the cortex
Wild-type ICR mice were used in this study
and the animals were purchased from SLC Japan and housed under standard conditions with food and water ad libitum and maintained on a 12-h light/dark cycle
Embryonic day (E) 0.5 was defined as 12:00 noon on the day when the vaginal plug was found
animals were deeply anesthetized by intraperitoneal injection of a combination anesthetic (MMB: 0.3 mg/kg of medetomidine
and 5.0 mg/kg of butorphanol) and intracardially perfused with ice-cold phosphate buffered saline (PBS) followed by 4% paraformaldehyde (PFA)
Whole brains were carefully dissected after perfusion and post-fixed in 4% PFA overnight at 4°C
then transferred to 30% sucrose solution (≥24 h or until brain sinks to the bottom of the tube at 4°C)
the embryos were collected from pregnant dams (wild-type ICR) and the brains were immediately dissected from the embryos and post-fixed in 4% PFA overnight at 4°C
The dams were sacrificed with cervical dislocation after administration of five doses of MMB
All animal experiments were approved by the Animal Research Committee of University of Fukui and the Animal Experimentation Committee of Osaka University
and performed in accordance with the Regulations for Animal Research at the University of Fukui and the Regulations on Animal Experimentation at Osaka University
Postnatal day (PD) 2 and 3-week-old (PW3) mice were used in the retrograde tracing experiments. PW3 mice were anesthetized and fixed on a stereotaxic frame, and tracer was injected into the cortex according to coordinates determined based on the mouse brain atlas (Paxinos and Franklin, 2008)
Tracer used in this study was 2% Fluoro-Gold (Fluorochrome) in distilled water; 0.5% Cholera Toxin Subunit B conjugated with AlexaFluor 488 (Thermo Fisher Scientific) in PBS; or 2% Green RetroBeadsTM IX (Lumaflour) in PBS
and all tracer mixtures were added with 0.1 μg/ml Fast Green
the anterior/posterior (AP) coordinates were referenced from Bregma
the medial/lateral (ML) coordinates were the distance from the midline at Bregma
and the dorsal/ventral (DV) coordinates were measured from the pial surface of the brain
All measurement units were in mm and are referred to in the following description as [anterior/posterior (AP)
Three and six injection sites were selected for both M1 and S1
0.8); whereas the stereotaxic coordinates for injection into S1 were (0.0
Each animal received pressure injection (approximately 40 nl/site) of a tracer delivered via a glass needle (pulled and broken at the tip with forceps to make an opening with a diameter of 40–60 μm) attached to a Hamilton syringe
animals were transcardially perfused and the brains were processed as mentioned above
Images of the whole FG-injected brains were taken with a fluorescence stereomicroscope (MZ 10F
and only the brains that appeared to have sufficient injection were subsequently sectioned
The selected brains were embedded in O.C.T
compound (Sakura) and stored at −80°C
then cut into 14–16 μm sections on a coronal plane using a freezing microtome (Leica model CM3050S)
Sections were imaged with BZ-X700 (Keyence) using an appropriate filter cube for FG (ET DAPI/FluoroGold
the animals were anesthetized by hypothermia and tracer was injected by using a Picospritzer® II microinjector (Parker Hannifin
The injection targets (M1 and S1) were estimated based on parallel experiments whereby the injected mouse was raised to adulthood and injection sites in M1 and S1 were traced to confirm the point of injection
injection in M1 and S1 were estimated as referral points from the midline (x) and the most rostral edge of the cortex (y)
y: 2.0 mm; and S1 was x: 2.5–2.8 mm and y: 3.0–3.5 mm
The mice were let to recover on heated pads and returned to the dams for survival
The mice were perfused 2 days post-injection at PD4 and the brains were processed and imaged as mentioned above
The genes preferentially expressed in association neurons (projecting from S1 to ipsilateral M1) compared to those in callosal neurons [projecting from S1 to contralateral S1 (cS1)] were identified with DNA microarray screening
cortical layer 2/3 neurons were transfected with pCAGGS-tdTomato by performing in utero electroporation at E15.5
and the mice that had tdTomato labeling of cell bodies in S1 were used in the subsequent procedure
The retrograde tracer Green RetrobeadsTM IX was injected at PD21 into either M1 or cS1 with the help of red fluorescence of tdTomato in these areas (in axon terminals projecting from S1)
Mice were transcardially perfused with ice-cold PBS and the brains were dissected out
Fresh-frozen sections were cut at 10 μm
thaw-mounted onto glass slides covered with polyphenylene sulfide membrane and air-dried immediately
The labeled association neurons in layers 2/3
and labeled callosal neurons in layers 2/3 and 5 were collected from S1 (more than 1,000 cells each) using a laser-captured microdissection system (AS-LMD
Total RNAs were prepared using NucleoSpin RNA XS kit (Macherey-Nagel)
Biotin-labeled and fragmented using OvationTM Pico WTA System
Labeled cDNAs were hybridized to the GeneChip Mouse Gene 1.0 ST Array (Affymetrix
washing and scanning were performed with a GeneChip 3,000 7G system (Affymetrix
Raw signals were subjected to Log-transformation
and centering in order to obtain processed signals for cross-sample comparison
The candidate genes preferentially expressed in L6b were selected using Subio Platform (version 1.14
The microarray data were deposited at Gene Expression Omnibus (GEO) under the accession number GSE123351
cDNA fragments of Kcnab1 and Ctgf were PCR-amplified from mouse brain cDNA with the following primer pairs
Kcnab1-fwd.: 5′ GAAATGGGGTGCCAGAAA 3′; rev.: 5′ ATTGTACAGGGCCAGGCA 3′; Ctgf-fwd.: 5′ AGAGTGGAGCGCCTGTTCTA 3′; and rev.: 5′ ACTGGCAGAGTGGTGGTTCT 3′
In order to examine the expression pattern of Kcnab1 splicing variants Kcnab1.1
in situ probes were generated to specifically recognize each of the subunits
The primer sets used were as follows: Kcnab1.1-fwd.: 5′ CAGCCGAGATCACAGCCTG… 3′; rev.: 5′ CTGCTTTGCGGTGGACTCTT… 3′; Kcnab1.2-fwd.: 5′ ATAAACCTGCCTGTGCAGA… 3′; rev.: 5′ CATGCCTGTCTTTGCCTTG… 3′; Kcnab1.3-fwd.: 5′ AGGCAGATAGGAACTTCCAG… 3′; rev.: 5′ GCTCGCAGAGCTTTAGGT… 3′
Amplified fragments were cloned into pGEM-T vector (Promega)
In vitro transcription of cRNA probes was performed with T7 or SP6 RNA polymerase (Roche) using the template plasmids linearized with an appropriate restriction enzyme and RNA DIG labeling mix (Roche) according to the manufacturer’s instructions
In situ hybridization histochemistry (ISHH) was performed as described before (Yagi et al., 2016) using cryosections (14–16 μm) prepared from mice at E12.5
The cryosections were air dried for 1 h and fixed in 4% PFA in PBS for 10 min at room temperature
The sections were then incubated in 0.2 M HCl for 10 mins
followed by permeabilization with Proteinase K (7.9 μg/ml; Roche) digestion for 10 min at 37°C
Concentration and treatment duration of Proteinase K were halved for the brain samples younger than PD4
the sections were treated with acetic anhydride in 0.1 M triethanolamine for 10 min
The slides were rinsed with PBS in between each step
the sections were transferred to 5× saline sodium citrate (SSC) for 10 min or longer
Hybridization was carried out with the generated probes in hybridization buffer (50% formamide
200 μg/ml yeast tRNA) overnight for at least 16 h at 55°C
High-stringency washes were carried out in the following steps: 5× SSC
20 min at room temperature; 2× SSC
20 min at 65°C; two washes with 0.2× SSC
20 min at 65°C and lastly the slides were transferred to PBS at room temperature
Detection of specific hybridization was performed using anti-Digoxigenin coupled with alkaline phosphatase
and subsequently visualized using nitro blue tetrazolium chloride/5-bromo-4-chloro-3-indolyl-phosphate (NBT/BCIP)
Sense probes were used as negative controls and no signals were observed with the sense probes
Bright field images of the stained sections were taken with BZ-X700
Brain cryosections were prepared from adult mice (PW8–PW24) and the sections were processed accordingly for double immunofluorescence labeling
After air-drying for an hour at room temperature
the sections were treated with Tris EDTA buffer (pH 8.5) for 1 min at 105°C in the autoclave or for 30 min at 85°C in the water bath
three rinses) in PBS before blocking the sections with 5% normal donkey serum
The sections were then incubated in primary antibodies (diluted in blocking solution) overnight at 4°C
The primary antibodies used in this study were as follows: CaMKIIα (1:100; rabbit; GeneTex
This was followed by incubation in species-specific fluorescent secondary antibodies (Donkey anti-mouse IgG Alexa Fluor 568 and either Donkey anti-rabbit IgG Alexa Fluor 488 or Donkey anti-goat IgG Alexa Fluor 488
All secondary antibodies were diluted at 1:200 in PBS
Nuclear staining was performed using 4′,6-diamidino-2-phenylindole (DAPI)
Fluorescence signals were imaged with a laser scanning confocal microscope (LSM 880 with Airyscan
Immunohistochemistry against Fluoro-Gold was combined with ISHH
sections were incubated with anti-Fluoro-Gold (FG; 1:500; rabbit; Millipore
Immunoperoxidase labeling was performed using a Vectastain Elite ABC Kit (Vector) and a DAB detection kit (Vector) was used for detection
according to the manufacturer’s protocol
Mouse homologues for exons 1.2 and 1.3 of the human Kcnab1 gene were identified by T-BLAST-N search in Ensembl genome database (GRCm38.p6) with the human sequences as queries. The genomic regions encompassing the hit sequences and exon 2 were then subjected to exon/intron prediction with GeneWise
The identified sequences were deposited at the DNA Data Bank of Japan (DDBJ) under the accession numbers LC437679 for exon 1.2 and LC437680 for exon 1.3
The TPM (Transcripts per million) data for Kcnab1, Ctgf, Cplx3, and Nurr1 (Nr4a2) genes across 1809 individual cells isolated from the mouse primary visual cortex (V1) were obtained from the GEO (accession, GSE 71585; Tasic et al., 2016)
Genes were considered as being expressed in a cell when the TPM value in the cell was 10 or larger
The percentage of cells expressing Kcnab1 at two different expression levels (TPM ≥ 10 and TPM ≥ 100) was calculated for each of the eight broad types of cortical cells (astrocytes
The percentages were also calculated for glutamatergic neurons in different layers and seven classes of GABAergic neurons by combining the numbers of cells for primary cell types in each layer or class
The percentages of cells expressing each of the four genes were calculated for two primary cell types for L6b (Rgs12 and Sepinb11)
To specifically examine if Kcnab1 is expressed in GABAergic neurons in L6b
the percentages of cells expressing Kcnab1 among 41 cells (containing 33 glutamatergic neurons and eight GABAergic neurons) dissected from L6b of V1 were also calculated
Similar analyses were performed using other RNAseq data for the four genes across 3,005 individual cells isolated from mouse S1 and hippocampal CA1 (Zeisel et al., 2015). The annotated expression data (equivalent to the raw data in GEO with the accession GSE60361 except for the cell type annotations) were obtained from the website of Linnarsson lab
The percentages of Kcnab1-expressing cells (expression score ≥ 1) were calculated for Level-1 classes of cell types and for Level-2 classes of interneurons and pyramidal neurons
Those of cells expressing each of the four genes were calculated for L6b cells
The retrograde labeling experiments showed the same results when repeated with two other tracers; fluorescence conjugated-cholera toxin B (CTB) and Green RetroBeadsTM (data not shown)
Retrograde tracer injection in M1 of PW3 mouse brain labeled unilaterally-projecting Layer 6b (L6b)/SP neurons in primary somatosensory cortex (S1)
(A,D) Whole mount brain images in a bright field (left) and a fluorescent (right) views showing Fluoro-Gold (FG) injections into primary motor cortex (M1; A) and contralateral S1 (cS1; D) at PW3
(B) Coronal sections of the brain shown in (A) at the level of M1 (left) and S1 (right)
(C) Higher magnification view of the boxed area in (B)
(E) A coronal section of the brain shown in (D) at the level of S1
(F) Higher magnification view of the boxed area in (E)
(G,J) Whole mount brain images in a bright field (left) and a fluorescent (right) views showing FG injection into M1 (G) and cS1 (J) at PD2
(H) Coronal sections of the brain shown in (G) at the level of M1 (left) and S1 (right)
(I) Higher magnification views of the boxed area in (H)
(K) A coronal section of the brain shown in (J) at the level of S1
(L) Higher magnification views of the boxed area in (K)
and (L) indicate borders of cortical layers
We next asked if this projection pattern is consistent throughout postnatal development. When FG was injected at PD2, we found FG-labeled SP neurons at PD4 for tracing from M1 (Figures 1G–I), but not for tracing from cS1 (Figures 1J–L)
similar to the results in L6b neurons in PW3 animals
L6b/SP neurons in the S1 area projected their axons unilaterally to the M1 area
As we found that its expression was specific to SP in the embryonic stages (see below)
we focused on the analysis of Kcnab1 in this article
Microarray screening identified Kcnab1 and Ctgf as expressed in L6b
(A) Green RetroBeadsTM was injected into M1 (left panel) or cS1 (right panel) of the brains at PD21 that had been electroporated with pCAGGS-tdTomato at E15.5
Green and red fluorescent images were overlaid onto the bright field image
(B) Relative expression levels of Kcnab1 (blue) and Ctgf (orange) among association neurons in L2/3
and L6b and callosal neurons in L2/3 and L5 compared by microarray analysis
(C,D) In situ hybridization histochemistry (ISHH) for Kcnab1 (C) and Ctgf (D) was carried out on coronal sections of mouse brain at PD21
Higher magnification view of the boxed area is shown on the right of each panel
Dashed lines in these high magnification images indicate borders of cortical layers
500 μm and 100 μm for low and high magnifications
From our retrograde tracing experiments and microarray gene analysis
we were inclined to hypothesize that association neurons in L6b/SP were molecularly distinctive
brains that were injected with retrograde tracer were processed for ISHH and immunohistochemistry to confirm this hypothesis
at the neonatal stage (injection at PD2 and brains fixed at PD4)
a proportion of association neurons in L6b/SP expressed Kcnab1 (data not shown)
Since L6b/SP neurons with a unilateral projection expressed Kcnab1 at both the neonatal and postnatal stages, we set out to examine the onset of Kcnab1 expression in the mouse cortex and whether the expression pattern was maintained throughout development. First, we carried out ISHH for Kcnab1 on coronal sections of the mouse brain at different embryonic stages. Kcnab1 expression was observed in the SP as early as E14.5 (Figure 4)
Kcnab1 expression was consistently restricted to the SP
and not detected in other layers throughout embryonic development
Kcnab1 has an earlier onset in comparison to the established L6b/SP marker Ctgf
of which the earliest expression was detected at E16.5 among the stages tested
Kcnab1 expression in developing mouse cortex was detected as early as E14.5
(A) ISHH for Kcnab1 (a–d) and Ctgf (e–h) was carried out on coronal sections of the mouse brain at different embryonic stages (E12.5
Kcnab1 expression was observed starting at E14.5 and it began earlier when compared to Ctgf expression
(B) Higher magnification of boxed regions in (A)
Kcnab1 expression was restricted to the SP during the embryonic stage (b′–d′)
Together with the expression during the embryonic stage
these data showed that Kcnab1 is expressed in a bipartite manner: a stable expression in the L6b/SP throughout the cortical development and a dynamic expression in other layers that appears postnatally
Kcnab1 expression pattern changed during postnatal development
(A) ISHH for Kcnab1 was carried out on coronal sections of the mouse brain at selected postnatal stages (PD3
(B) Higher magnification view of boxed regions in (A)
Weak Kcnab1 expression was detected in deep layers above L6b at PD3 (a,a′)
Kcnab1 expression gradually spread to the more superficial layers and some cells with higher expression appeared (b,b′)
becoming evidently scattered in the upper layers at PD25 (c,c′)
Ctgf was limited to L6b throughout postnatal development (d–f; d′–f′)
Dashed lines in (c′) and (f′) indicate borders of cortical layers
Kcnab1-expressing neurons constitute a distinct subpopulation of L6b/SP neurons
This held true also for early postnatal stage PD3 (data not shown)
the expression pattern of Kcnab1 described in this study was explained by that of the variant 1.1 alone
Kcnab1 splice variant Kcnab1.1 was expressed in the mouse cortex
(A) Genomic structure of 5′ part of the Kcnab1 gene locus showing three alternative first exons (exons 1.1–1.3)
Filled and open bars indicate coding and non-coding part of the exons
(B) Amino acid sequence alignments of the three alternative N-terminals of the mouse (m) and human (h) Kvβ1 protein encoded by three alternative first exons
The residues in mKvβ1 different from those in hKvβ1 are shown in white letters on black background
(C) ISHH for Kcnab1 splice variants was carried out on PD25 mouse brain sections using the probes specific for exons 1.1–1.3
Only Kcnab1.1 expression was observed in the cortex (a)
Neither Kcnab1.2 nor Kcnab1.3 was present in any layers of any cortical areas (b,c)
Higher magnification of boxed regions in (a–c) is shown in (a′–c′)
Dashed lines indicate borders of cortical layers
500 μm (a–c); 100 μm (a′–c′)
The main findings of this study are: (1) that a discrete population of L6b/SP neurons project unilaterally from S1 to M1
and no callosal projection was observed; (2) that Kcnab1 identifies a proportion of this subclass of L6b/SP neurons with an inter-areal projection; (3) that Kcnab1 is co-expressed with known L6b/SP markers Ctgf
and Nurr1 to different degrees at postnatal stage; and (4) that Kcnab1 expression is restricted to L6b/SP during the early developmental stage but scattered Kcnab1-positive neurons were observed in the upper layers of postnatal cortices
it would be most ideal if the tracing experiment is repeated with transgenic reporter line that would allow further characterization of the association neuron subclass
the axon trajectory that originates from this area
and their targets that may include other cortical regions
we have identified a group of L6b/SP association neurons that expressed a specific splice variant of Kcnab1
and the expression in L6b/SP was maintained at all developmental stages
This molecular authenticity that spans development could be a plausible mechanism that modulates L6b/SP neuron specification during cortical maturation
and this would add to the increasing efforts to characterize L6b/SP neurons
thus elucidating the role of L6b/SP neurons in SP development
and subsequent brain network establishment
All animal experiments were approved by Animal Research Committee of University of Fukui and Animal Experimentation Committee of Osaka University
and performed in accordance with Regulations for Animal Research at University of Fukui and Regulations on Animal Experimentation at Osaka University
This work was supported by grants from Takeda Science Foundation
NOVARTIS Foundation (Japan) for the Promotion of Science
and Japan Society for the Promotion of Science (JSPS) KAKENHI [Grant numbers JP23800027
JP26830027 and JP17K07076 (to YO) and JP15K15015
ST was supported by The Ministry of Education
Malaysia (University of Malaya HLCB/PK 2015)
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest
The microarray screening was supported by the Division of Bioresearch of Life Science Research Laboratory
Animal experiments were supported by both the Division Laboratory Animal Resources of Life Science Research Laboratory
University of Fukui and The Institute of Experimental Animal Science
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fnana.2019.00039/full#supplementary-material
a transient neocortical structure: its role in the development of connections between thalamus and cortex
Glutamatergic nonpyramidal neurons from neocortical layer VI and their comparison with pyramidal and spiny stellate neurons
Relation between putative transmitter phenotypes and connectivity of subplate neurons during cerebral cortical development
Organization and development of corticocortical associative neurons expressing the orphan nuclear receptor Nurr1
Development of layer I and the subplate in the rat neocortex
A transcriptomic atlas of mouse neocortical layers
Contrasting patterns in the localization of glutamic acid decarboxylase and Ca2+/calmodulin protein kinase gene expression in the rat central nervous system
Long-range projections from sparse populations of GABAergic neurons in murine subplate
doi: 10.1002/cne.24592 [Epub ahead of print]
reciprocal pathway between the lateral geniculate nucleus and visual cortex in the macaque monkey
Morphological heterogeneity of layer VI neurons in mouse barrel cortex
axonal projection and position define the transcriptional identity of individual neocortical projection neurons
Transient cells of the developing mammalian telencephalon are peptide-immunoreactive neurons
Interstitial cells of the adult neocortical white matter are the remnant of the early generated subplate neuron population
Widespread projections from subgriseal neurons (layer VII) to layer I in adult rat cortex
doi: 10.1002/(SICI)1096-9861(19990503)407:2<275::AID-CNE8>3.0.CO;2-0
Layer-specific programs of development in neocortical projection neurons
Inward and delayed outward membrane currents in isolated neural somata under voltage clamp
Growth and targeting of subplate axons and establishment of major cortical pathways
Del Río
Developmental history of the subplate and developing white matter in the murine neocortex
neuronal organization and relationship with the main afferent systems at embryonic and perinatal stages
Distinct translaminar glutamatergic circuits to GABAergic interneurons in the neonatal auditory cortex
Rapid developmental switch in the mechanisms driving early cortical columnar networks
A novel K+ channel β-subunit (hKvβ1.3) is produced via alternative mRNA splicing
Major glutamatergic projection from subplate into visual cortex during development
doi: 10.1002/(SICI)1096-9861(19980817)398:1<105::AID-CNE7>3.0.CO;2-5
Functional synaptic circuits in the subplate during fetal and early postnatal development of cat visual cortex
Changing patterns of synaptic input to subplate and cortical plate during development of visual cortex
The changing roles of neurons in the cortical subplate
Requirement for subplate neurons in the formation of thalamocortical connections
A role for subplate neurons in the patterning of connections from thalamus to neocortex
PubMed Abstract | Google Scholar
spike broadening and after-hyperpolarization in Kvbeta1.1-deficient mice with impaired learning
Functional synaptic projections onto subplate neurons in neonatal rat somatosensory cortex
Connective tissue growth factor: a novel marker of layer vii neurons in the rat cerebral cortex
Hoerder-Suabedissen
Subset of cortical layer 6b neurons selectively innervates higher order thalamic nuclei in mice
Hoerder-Suabedissen
Morphology of mouse subplate cells with identified projection targets changes with age
Hoerder-Suabedissen
Molecular diversity of early-born subplate neurons
Hoerder-Suabedissen
evolution and pathology of neocortical subplate neurons
Hoerder-Suabedissen
Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophrenia
Hoerder-Suabedissen
Novel markers reveal subpopulations of subplate neurons in the murine cerebral cortex
Alpha calcium/calmodulin-dependent protein kinase II selectively expressed in a subpopulation of excitatory neurons in monkey sensory-motor cortex: comparison with GAD-67 expression
Subplate neurons: crucial regulators of cortical development and plasticity
Role of subplate neurons in functional maturation of visual cortical columns
Subplate neurons regulate maturation of cortical inhibition and outcome of ocular dominance plasticity
Corticothalamic projections from the rat primary somatosensory cortex
Developmental history of the transient subplate zone in the visual and somatosensory cortex of the macaque monkey and human brain
Inter- and intralaminar subcircuits of excitatory and inhibitory neurons in layer 6a of the rat barrel cortex
Subplate neuron ablation alters neurotrophin expression and ocular dominance column formation
Activity-dependent Nurr1 and NGFI-B gene expression in adult mouse olfactory bulb
Subplate cells: amplifiers of neuronal activity in the developing cerebral cortex
The superior function of the subplate in early neocortical development
Cellular physiology of the neonatal rat cerebral cortex: intrinsic membrane properties
doi: 10.1002/1097-4547(20001115)62:4<574::aid-jnr12>3.0.co;2-0
Gli3 controls subplate formation and growth of cortical axons
Morphology and physiology of excitatory neurons in layer 6b of the somatosensory rat barrel cortex
Neocortical layer 6B as a remnant of the subplate—a morphological comparison
Subplate neurons pioneer the first axon pathway from the cerebral cortex
Alternative splicing of the human Shaker K+channel β1 gene and functional expression of the β2 gene product
Synaptogenesis in purified cortical subplate neurons
Transcriptional landscape of the prenatal human brain
Large-scale maintenance of dual projections by callosal and frontal cortical projection neurons in adult mice
Mechanisms underlying the early establishment of thalamocortical connections in the rat
synaptic plasticity and learning in aged Kvβ1.1 knockout mice
Gene expression analysis of the embryonic subplate
Gene expression profiling of preplate neurons destined for the subplate: genes involved in transcription
steroid hormone signaling and neuronal survival
hPSC modeling reveals that fate selection of cortical deep projection neurons occurs in the subplate
Timing and origin of the first cortical axons to project through the corpus callosum and the subsequent emergence of callosal projection cells in mouse
doi: 10.1002/(sici)1096-9861(19981019)400:2<197::aid-cne3>3.0.co;2-4
The Mouse Brain in Stereotaxic Coordinates
Google Scholar
Extracortical origin of some murine subplate cell populations
Intracortical connectivity of layer VI pyramidal neurons in the somatosensory cortex of normal and barrelless mice
Dynamic integration of subplate neurons into the cortical barrel field circuitry during postnatal development in the Golli-tau-eGFP (GTE) mouse
Cell-type-specific activity in prefrontal cortex during goal-directed behavior
Cortical layer VII and persistent subplate cells in mammalian brains
Do subplate neurons comprise a transient population of cells in developing neocortex of rats
doi: 10.1002/1096-9861(20001030)426:4<632::AID-CNE10>3.0.CO;2-4
Thalamic nuclei convey diverse contextual information to layer 1 of visual cortex
Kvβ1 subunit binding specific for Shaker-related potassium channel α subunits
Correlated gene expression and target specificity demonstrate excitatory projection neuron diversity
Adult mouse cortical cell taxonomy revealed by single cell transcriptomics
PubMed Abstract | CrossRef Full Text | Google Scholar
Subplate neurons promote spindle bursts and thalamocortical patterning in the neonatal rat somatosensory cortex
Specificity in the axonal connections of layer VI neurons in tree shrew striate cortex: evidence for distinct granular and supragranular systems
Persistence of early-generated neurons in the rodent subplate: assessment of cell death in neocortex during the early postnatal period
Vélez-Fort
The stimulus selectivity and connectivity of layer six principal cells reveals cortical microcircuits underlying visual processing
Molecularly defined subplate neurons project both to thalamocortical recipient layers and thalamus
Comparative aspects of subplate zone studied with gene expression in sauropsids and mammals
Distribution of CaMKIIα expression in the brain in vivo
Filamin A interacting protein plays a role in proper positioning of callosal projection neurons in the cortex
Spindle bursts in neonatal rat cerebral cortex
Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq
Intracortical axonal projections of lamina VI cells of the primary somatosensory cortex in the rat: a single-cell labeling study
Novel interneuronal network in the mouse posterior piriform cortex
Functional excitatory microcircuits in neonatal cortex connect thalamus and layer 4
Akiyama H and Sato M (2019) Kcnab1 Is Expressed in Subplate Neurons With Unilateral Long-Range Inter-Areal Projections
Received: 10 December 2018; Accepted: 20 March 2019; Published: 03 May 2019
Copyright © 2019 Tiong, Oka, Sasaki, Taniguchi, Doi, Akiyama and Sato. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY)
*Correspondence: Makoto Sato, bWFrb3NhdG9AYW5hdDIubWVkLm9zYWthLXUuYWMuanA=
† These authors have contributed equally to this work
senior vice-president for marketing in products and markets at Seagate
to look at how spinning disk can get to 40TB and 50TB
We talk about hard disk drive technologies such as heat-assisted magnetic recording (HAMR) that can boost areal density and pack more data onto disk platters
Feist also talks about the future of hard disk drives (HDDs) and the use cases suited to them
Great question. Thanks for the time this morning. It’s just an amazing time to be part of the hard drive industry
and with all of the markets starting to rebound
it’s a great time to innovate and provide the ability to have data storage devices at scale
The innovations that are underway right now are driven by a lot of contributions across many different disciplines
We have great engineers working in our supply chain to allow us to have mechanical innovations
to have recording physics innovations with magnetic recording
and to put more information on every disk inside a hard drive
And we have amazing wafer and media metrology underway to continue to improve our process control
our repeatability and our ability to extract more areal density out of every drive
Areal density is really what’s at the forefront of development for hard drives
• Download this podcast •
It has been for years and will continue to be for years to come
and there’s a number of new techniques and new processes that we have access to
with technologies that are now becoming more readily available
[These include] better simulation, more use of GPUs [graphics processing units] to do things with artificial intelligence [AI] to allow us to find design spaces that we didn’t have access to before with speed
and all that creates a recipe that our engineers are taking advantage of and allowing us to bring larger and larger capacity drives to our customers
We’ve seen the hard drive industry bring forth 28TB hard drives and we’ve seen Seagate deliver 3TB per platter samples to the industry
and I think as an industry we’ll continue to drive that areal density in that terabyte per disk increase
We’ll see delivery of 4TB per disk and 5TB per disk in the not too distant future
All of that served on a 10-disk hard disk drive itself, so delivering 40TB and 50TB disk drives in the near future. Really, really exciting. The basis for those capacity increases are really driven by heat-assisted magnetic recording (HAMR) innovation
investment and development over the last 15 to 20 years
Just as perpendicular recording had served the hard drive industry for the last 20 years
we believe that HAMR will serve the industry for years to come
All of this really comes at the right time
in the sense that cloud storage demand is growing and the use of cloud continues to grow
the demand curve really helps us continue to stay focused on that innovation and make sure we’re delivering larger hard drives to meet that use case
This is a question that we get asked routinely
It’s one that we have a lot of fun answering in the sense that we work very closely with the largest customers in the world and we have a diverse set of customers
We have a video and information and analytics business
All of these routes to market are slightly different and they all have the need for increasing data storage
It’s exciting and the new use cases that you hear a lot about
It shows the importance and the relevance of data on making decisions and creating a society that’s informed and has data at their fingertips
The innovation is underway now and you’re going to see a significant transformation in how large capacity drives are used and how clouds take advantage of those economies of scale
You can see new businesses depending on hard drives for their ecosystem development
social media companies and the growth of video are all very well suited to what hard drives provide: very large capacity
efficient sustainable storage architectures
scalable architectures that allow us to have presence in multiple geographies around the globe
[And] there are new use cases with all of these video applications for prosumers and content creators
which are now taking advantage of tools with generative AI to do text-to-video and creating larger
All those things are good for data storage and HDDs have been
the backbone of data storage needs at exabyte scale
Organizations must take steps to ensure compliance with emerging rules targeting foreign adversaries' access to U.S
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landowner face off over removal of barbed wire fencing in tenanted field; posse of policemen
and MLA rush to avert law and order situation; Police seek ownership documents from tenant
Tension rent the air at Sao Jose de Areal after local residents protested over the damage to a barbed wire fencing in a tenanted land apparently to make way to the statue of Shivaji Maharaj
The barbed wire fencing and stones damaged
MARGAOAhead of the Shiv Jayanti celebrations on February 19
tension rent the air at Sao Jose de Areal on Monday
bringing face to face the local residents and the landowner Mehboob Makandar over the damage and removal of barbed wire fencing in a tenanted field apparently to pave way for an access to the adjoining property playing host to the statue
A team of Maina-Curtorim police led by PI Arun Desai rushed to Areal with a posse of policemen to avert a law and order situation
The police were later joined by Salcete Mamlatdar Vimod Dalal to work out a solution
Velim MLA Cruz Silva also made his presence at the site later in the evening
The area had witnessed tension and violence last year around the same time after a group of persons carried Shivaji’s statue for installation on a hilly land
Local residents maintained they are neither against Shivaji Maharaj nor his statue
they insisted the core issue facing Benabhat is not Shivaji’s statue
Tension started on Monday noon after local residents rushed to Benabhat following reports that the owner of the adjoining plot
where a statue of Shivaji Maharaj was installed in his property last year
allegedly started clearing the fencing in a tenanted field ahead of his plot
Landowner Makandar told the media that he had come to his property in view of the Shiv Jayanti celebrations scheduled on Wednesday
only to find barricading and fencing of the plot in question
the local residents came in large numbers and stopped us
They also blocked my car by placing stones near the tyres,” he said
who claimed to be the tenant of the plot in question
said he had fenced his plot as he had cultivated paddy and had drawn up plans to go for the second crop
He alleged that the fencing and barricading was dismantled and damaged and demanded restoration of his barbed wire fencing
Local residents questioned PI Arun Desai when he asked the tenant Cruz Tereza to produce his document
claiming tenancy or land ownership to the barricade plot in question
insisting that the police officer should first ask Mehboob Makandar to produce documents or any order authorising him to enter the tenanted plot and remove the fencing
Another property owner grants consent for alternate access to Shivaji statue
MARGAO: After discussions between the authorities and the local residents and the Shiv Premis
it was finally agreed to use an alternate access to go to the statue of Shivaji Maharaj on Shiv Jayanti celebration on February 19
Bajrang Dal leader Viraj Desai and Salcete Mamlatdar Vimod Dalal later told the media that the issue over the access to the Shivaji statue has been resolved after an owner of an alternate property has consented to provide access to the statue from his property
Bajrang Dal leader Viraj Desai said the organisation has agreed to the alternate access to the Shivaji statue
even though he said nothing would have prevented its members from going to the statue through the other property
Out of respect for law and the advice of the authorities
we have accepted the alternate route,” he said
He added: “The Shivaji statue at Sao Jose de Areal would have been a perfect example of community harmony in Goa
the land to install Shivaji statue has been provided by a Muslim owner and the village is inhabited by the Christian population
Shiv Jayanti is a victory celebration and an important event for the Hindus
We do not know why the people are creating issues over the statue and land access,” he said
This includes the following streams and drainages… Dodd Creek
– Some locations that will experience flooding include…Floyd
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HOLOPLOT’s X1 system was chosen to provide the sound for The Atmosphere stage at Tomorrowland
a custom-made circus-top tent featuring DJs
The system utilised two main arrays consisting of six X1 modules each
The key challenges to overcome were the highly reflective surfaces causing echoes in the listening area
preventing an even sweet spot to fully benefit from the immersive content played at the stage
Sound Engineer at Noizboyz and Co-Founder of stereo upmixing solution Areal
is responsible for the sound design of all 16 stages at Tomorrowland and chose the HOLOPLOT system for the audio experience at Atmosphere
“I was really shocked with the sound quality that was achievable because I expected beamforming to decrease it,” he said
It’s amazing how the quality rises when you just focus audio on the people and don’t create any reflections
and that improves the immersive experience
In the spirit of technological advancement
had already developed a new piece of software
allowing them to upmix stereo signals into multi-channel content in real time
This had been used at Atmosphere for a couple of years already
but the size of the tent and the required distributed system had still proven challenging for the designers in the past
with the additional loudspeakers needed to achieve the surround sound effects causing increased reflections and confusion in the diffuse field
delivering the results of the upmixed content via Areal to the crowd without echos
Enabling this are the two core pillars of HOLOPLOT technology
3D Audio-Beamforming and Wave Field Synthesis
“Both allow us to control sound in the 3D space,” stated Sebastian Boeldt
“We can precisely shape the coverage areas in the audience zone
but also avoid certain shapes of the venue
minimising reflections and improving the clarity of the performance.”
also allows the precise gain and delay alignment between them
“This means we can increase the immersive sweet spot and minimize the delay spread
a key parameter when designing immersive systems,” Boeldt explained
“The combination of sound control via avoidance of the tent surfaces and division of the crowd into time aligned coverage zones create a perfect base canvas for the Areal technology to shine
It’s a really flexible piece of software that paired beautifully with the X1 system.”
“The widespread misconception that loud is always better doesn’t apply here
and thanks to the isolated yet aligned zones X1 created and the multi-channel content from the Areal engine we achieved great results
giving that small immersive club feeling,” concluded Doms
holoplot.com
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Volume 7 - 2019 | https://doi.org/10.3389/fchem.2019.00869
This article is part of the Research TopicNext-generation Electrochemical Energy Storage DevicesView all 13 articles
Self-supported electrodes represent a novel architecture for better performing lithium ion batteries
lower areal capacity restricts their commercial application
we explore a facial strategy to increase the areal capacity without sacrificing the lithium storage performance
A hierarchical CuO–Ge hybrid film electrode will not only provide high areal capacity but also outstanding lithium storage performance for lithium ion battery anode
Benefiting from the favorable structural advance as well as the synergic effect of the Ge film and CuO NWs array
the hybrid electrode exhibits a high areal capacity up to 3.81 mA h cm−2
good cycling stability (a capacity retention of 90.5% after 150 cycles)
and superior rate performance (77.4% capacity remains even when the current density increased to 10 times higher)
There is an increasing concern about fabricating self-supporting electrodes with high areal capacity as well as good electrochemical performance
Usually, the self-supporting electrodes cannot maintain good electrochemical performance at very high areal capacity. Herein, we report a hierarchical CuO–Ge hybrid film on CF as a self-supporting electrode with ultrahigh areal capacity for LIB application. As shown in Figure 1
the integrated film was formed by physical vapor deposition of Ge film on CuO NWs array
which were grown directly on the CF via a facial and scalable solution approach
CuO NWs array with well-defined nanostructure serves as both the active materials and conductive connection for Ge film
The porous feature will not only alleviate the drastic volume change during the Li insertion and extraction process but also facilitate the diffusion of electrolyte into the electrode
Benefiting from the favorable nanostructures as well as the synergic effect of the Ge film and CuO NWs array
the integrated electrode delivers ultrahigh areal capacity
this is the first time that CuO NWs combined with Ge film hybrid anode achieved a high areal capacity
It could deliver an ultrahigh charge areal capacity up to 3.45 mA h cm−2 after 150 cycles at a current density of 0.8 mA cm−2 and a capacity ~2.98 mA h cm−2 at a current density as high as 4 mA cm−2
Schematic illustration of the fabrication processes of the CuO–Ge hybrid film on Cu foam (CF)
The CuO NWs array on CF was placed into an radio frequency (RF) sputtering system (Verios G4 UC
Shenyang Lining Co.) using 99.999% pure Ge target
The base pressure was 7.8 × 10−4 Pa
The mass loading of CuO NWs supported Ge (typically ~0.67 mg cm−2)
CuO NWs array (typically ~3.64 mg cm−2) and Ge on pristine CF (typically ~0.45 mg cm−2) were weighed before and after sputtering using a microbalance (OHAUS
the Ge film was also deposited on pristine CF under the same deposition parameters
The samples were characterized using X-ray diffraction (Rigaku Ultima IV) and Raman spectroscopy (WITEC alpha300 R Confocal Raman system)
and the structure and morphology characterization of them were carried out by field-emission scanning electron microscopy (SEM
FEI Inspect F50) with accelerating voltage of 5.00 kV and transmission electron microscopy (TEM
CR 2032-type coin cells was used to test electrochemical characterizations
test cells were assembled in a high-purity argon filled glove box (Mikrouna Technology) with oxygen and moisture level <0.5 ppm
The fabricated self-supporting electrodes were used as the working electrode and a Li foil as the counter and reference electrode
Lithium hexafluorophosphate (LiPF6) (1 M) in a mixture of ethylene carbonate and diethyl carbonate (1:1 in volume) was used as the electrolyte
All the cells were aged for 12 h so that the electrolyte can fully infiltrate the whole cell before measurement
Lithium storage performance were evaluated by a multichannel battery tester (Neware
BTS-610) in the voltage range of 3.0–0.01 V (Li/Li+)
Shanghai Chenhua Co.) was used to evaluate the cyclic voltammetry (CV) at scan rate of 0.1 mV s−1
All the tests were carried out in the thermotank at fixed temperature of 25°C
One can note that the strong diffraction peaks of 43.3
which could be indexed to the CF with JCPDS card no
There are two weak but identifiable peaks located at 35.5 and 38.8°
corresponding to the (−111) and (111) planes of the monoclinic CuO
and CuO–Ge hybrid film; (B) X-ray diffraction (XRD) pattern of the CuO–Ge hybrid film
(A,B) The top and (C) side view SEM images of CuO NWs array; (D,E) The top and (F) side view SEM images of the CuO–Ge hybrid film
We also present the TEM images of the CuO–Ge hybrid film in Figure 4A. The obtained distributions of Cu and Ge are shown in Figure 4B
the energy dispersive spectroscopy mapping profile obviously pictures that the outer sheath consists of Ge
whereas Cu is perfectly populated in the inner part of the CuO–Ge hybrid film
and the Ge films were grown uniformly and was deposited onto the whole CuO NWs
(A) Annual dark-field TEM image of the CuO–Ge hybrid film; (B) elemental mapping of CuO–Ge hybrid film: the corresponding Cu
the Coulombic efficiency of the battery was all above 99.2%
the first discharge and charge capacities are 3.34 and 2.50 mA h cm−2 for CuO NWs array and 0.71 and 0.59 mA h cm−2 for Ge film
The CuO–Ge hybrid film electrode exhibits much higher initial charging areal capacity when compared with the sum of the Ge film and CuO NWs array electrode
This is because the mass loading of the Ge film on CuO NWs array is higher than that on CF attribute to the larger surface area of the CuO NWs array
demonstrating the structural advantages of the CuO NWs array
(A) The initial voltage profiles of the CuO–Ge hybrid film
and Ge film; (B) the cycle performance of the CuO–Ge hybrid film
and Ge film; (C) the initial five cyclic voltammetry (CV) curves of the CuO–Ge hybrid film; (D) rate performance of CuO–Ge hybrid film
Figure 5B compares the cycle performance of the CuO–Ge hybrid film
CuO NWs array and Ge film for subsequent 150 cycles at a high current density of 0.8 mA cm−2
For the CuO–Ge synthesized film electrode
a reversible discharge capacity of 3.81 mA h cm−2 was achieved at the second cycle
corresponding to a specific capacity of 883 mA h g−1
The electrode could still deliver a high areal capacity of ~3.45 mA h cm−2 with a capacity retention of 90.5% after 150 cycles (the corresponding specific capacity contribution from Ge was 1,462 mA h g−1
the CuO NWs array electrode could deliver a capacity of 2.47 mA h cm−2 after 150 cycles
which corresponds to the 90.0% of the original one
While Ge film can only obtain a reversible capacity of 0.2 mA h cm−2 after 150 cycles with a much lower capacity retention of 59.3%
The CuO–Ge hybrid film electrode exhibits a superior improvement in Li storage performance compared to the other electrodes
which may be attribute to the novel structure design using a hierarchical 3D nanostructure to combine two high theoretical capacity materials
The well-separated CuO NW arrays will not only provide large area for larger mass loading of Ge but also the large void space to overcome the large volume change during charge and discharge
The CV curves were well-overlapped with each other from the second cycle afterwards
suggesting that the electrode has a good reversibility
The rate capability is further tested for the CuO–Ge hybrid film electrode, which is of significant importance for high power energy storage. The rate performance was evaluated by charging–discharging at varied current densities varying from 0.4 to 4 mA cm−2. As shown in Figure 5D
after the first five cycles at the current density of 0.4 mA cm−2
the obtained electrode showed a high discharge areal capacity of 3.85 m A h cm−2; then
it slightly reduced to 3.68 and 3.45 m A h cm−2 at current rates of 0.8 and 1.6 mA cm−2
Even at a rate as high as 4 mA cm−2
the CuO–Ge hybrid film could still deliver a reversible capacity of ~2.98 m A h cm−2
corresponding to the 77.4% capacity of the capacity at 0.4 mA cm−2
After the rate returned back to the initial value of 0.4 mA cm−2 for five cycles
94.5% of the initial charge capacity was regained
and eventually obtained a capacity of 2.59 m A h cm−2
Indicating the benefit from the favorable nanostructures as well as the synergic effect of the Ge film and CuO NWs array
the hybrid electrode hybrid film electrode has wonderful rate capability far beyond the CuO NWs and Ge film electrode
(A,B) SEM images of the CuO–Ge hybrid film after 50 cycles
an efficient strategy to prepare self-supporting electrode with ultrahigh areal capacity for LIB application has been introduced
The obtained CuO–Ge hybrid film electrode exhibits excellent lithium storage performance
It can deliver a high areal capacity of 3.81 mA h cm−2 after 150 cycles
corresponding to 90.5% of the original one
the electrode could deliver high areal capacities of 2.98 mA h cm−2 even at ultrahigh current density of 4 mA cm−2
The hierarchical CuO–Ge hybrid film grown directly on CF could be a novel substitute of graphite for LIBs
and the facial and efficiency synthesis strategy sheds light on improving the areal capacity of the self-supporting electrodes
which can be applicable for preparation of other high capacity hybrid electrode for energy storage application
All datasets generated for this study are included in the article/supplementary material
All authors have contributed in various degrees to the analytical methods used
or to revise it critically for important intellectual content
This work was supported by the National Natural Science Foundation of China (grant number 11704071)
the Excellent Youth Foundation of Fujian Scientific Committee (grant number 2019J06008)
the Natural Science Foundation of Fujian Province
and the Award Program for Fujian Minjiang Scholar Professorship
Construction of carbon nanoflakes shell on CuO nanowires core as enhanced core/shell arrays anode of lithium ion batteries
High capacity Li ion battery anodes using ge nanowires
Lithium-ion battery anodes of stacked nanowire laminate for ultrahigh areal capacities
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Copper germanate nanowire/reduced graphene oxide anode materials for high energy lithium-ion batteries
In-situ oxidized copper-based hybrid film on carbon cloth as flexible anode for high performance lithium-ion batteries
Solution-grown germanium nanowire anodes for lithium-ion batteries
Hierarchical structures based on two-dimensional nanomaterials for rechargeable lithium batteries
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Facile fabrication of MOF-derived octahedral CuO wrapped 3D graphene network as binder-free anode for high performance lithium-ion batteries
Multi-layer CuO@NiO hollow spheres: microwave-assisted metal-organic-framework derivation and highly reversible structure-matched stepwise lithium storage
Flexible 3D porous CuO nanowire arrays for enzymeless glucose sensing: in situ engineered versus ex situ piled
Surface-stabilized amorphous germanium nanoparticles for lithium-storage material
Electrodeposited germanium/carbon composite as an anode material for lithium ion batteries
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In situ synthesis of Cu2O–CuO–C supported on copper foam as a superior binder-free anode for long-cycle lithium-ion batteries
Nanoporous germanium as high-capacity lithium-ion battery anode
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Cu3Ge/Ge@C nanocomposites crosslinked by the in situ formed carbon nanotubes for high-rate lithium storage
Germanium nanoparticles supported by 3D ordered macroporous nickel frameworks as high-performance free-standing anodes for Li-ion batteries
Flexible dimensional control of high-capacity Li-ion-battery anodes: from 0D hollow to 3D porous germanium nanoparticle assemblies
Gaining cycling stability of Si- and Ge-based negative Li-ion high areal capacity electrodes by using carbon nanowall scaffolds
Synthesis of tin catalyzed silicon and germanium nanowires in a solvent–vapor system and optimization of the seed/nanowire interface for dual lithium cycling
Germanium-graphene composite anode for high-energy lithium batteries with long cycle life
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High electrochemical performance based on ultrathin porous CuO nanobelts grown on Cu substrate as integrated electrode
Vertically aligned CNT-supported thick Ge films as high-performance 3D anodes for lithium ion batteries
Facile synthesis of CuO mesocrystal/MWCNT composites as anode materials for high areal capacity lithium ion batteries
doi: 10.1002/(SICI)1097-4555(199905)30:5<413::AID-JRS387>3.0.CO;2-N
Stabilizing Si/graphite composites with Cu and in situ synthesized carbon nanotubes for high-performance Li-ion battery anodes
Dendrite-free Li metal plating/stripping onto three-dimensional vertical-graphene@carbon-cloth host
Mesoporous germanium as anode material of high capacity and good cycling prepared by a mechanochemical reaction
Germanium anode with lithiated-copper-oxide nanorods as an electronic-conductor for high-performance lithium-ion batteries
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Wang X and Cheng S (2020) A Hierarchical Copper Oxide–Germanium Hybrid Film for High Areal Capacity Lithium Ion Batteries
Received: 16 October 2019; Accepted: 03 December 2019; Published: 08 January 2020
Copyright © 2020 Deng, Li, Li, Cai, Wang, Zhang, Jia, Wang and Cheng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY)
*Correspondence: Xinghui Wang, c2VhcGh5MjNAZnp1LmVkdS5jbg==; Shuying Cheng, c3ljaGVuZ0BmenUuZWR1LmNu
research in the humanities and social sciences is constrained or even prevented
and the people with whom researchers come into contact for their work are sometimes threatened or endangered
there are a growing number of exogenous constraints (security
political and economic) which place both the right to investigate and the rights of those being investigated in tension: by preventing or restricting access to the research field upstream
by putting researchers and their respondents in difficulty
and by also exposing them to risks on their return
particularly in the restitution and valorization of their work
an initial Inalco survey entitled "Research
training and expertise in "prevented" or "hindered" fields: practices
methods and new resources" was launched in February 2024
Its results are based on the responses of over 400 researchers and young researchers in areal studies
They made it possible to objectify knowledge of their research and data collection practices in "impeded"
"hindered" or more broadly "constrained" terrains
and their expectations in terms of training
institutional support and knowledge sharing
The first results, published in December 2024
highlight the entrenchment of constraints (political-administrative
situational) and their impact on research practices: whether in terms of the conditions (notably financial and institutional) in which it is carried out
the environment in which it is embedded (creating
new forms of interaction with local partners)
or the cross-fertilized methodologies it presupposes
The second part of this investigation is now underway, in the form of workshops conducted with the Études aréales unit (UAR 2999) as part of the "Terrains contraints" mission
2024 by CNRS SHS to its aréaux networks in collaboration with Inalco
This mission intends to reflect on the best ways to support researchers in their practices
and propose concrete recommendations in this area to the entire scientific community
aimed at clarifying and completing the results of the survey
Locals question police action despite agreement over alternate route for Shiv Jayanti celebrations
Residents of Sao Jose de Areal and police come face to face at Benabhat after the cops stopped the tenant from re-erecting his fencing which was damaged on Monday
MARGAOTension rent the air at Sao Jose de Areal again on Tuesday evening after the police and other authorities prevented the tenant from re-erecting fencing on his tenanted field at Benabhat
despite a solution worked out by the authorities on Monday that visitors to the statue of Shivaji Maharaj would use an alternate access
Areal residents rushed to the site in support of the tenant
suspecting that the police were stopping the fencing work to pave the way for visitors to go to the Shivaji statue through the tenanted field
and Salcete Mamlatdar Vimod Dalal rushed to Benabhat-Areal
and villagers also descended at the site and questioned the police and other authorities for obstructing the tenant from completing the fencing work
The Velim MLA reminded the police that the authorities and the parties had all agreed on Monday that an alternate access would be used to go to Shivaji’s statue at Benabhat
He wondered why the police were preventing the tenant from erecting the barbed wire fencing in his tenanted field
raising fears about whether there was any plan to use the tenanted field to go to the statue on Wednesday during Shiv Jayanti celebrations
The police team were heard requesting the tenant Cruz Tereza to keep the barbed wire fencing work on hold for a day or two
only fuelling suspicions among the locals about whether there was any hidden agenda by the authorities to allow visitors to use the tenanted field to make it to the Shivaji statue on Wednesday to celebrate Shiv Jayanti
Velim MLA Cruz Silva told the media that the District Collector Egna Cleetus had later told the police to allow visitors to the Shivaji statue only through the alternate access
Collector directs cops to stick to alternate route arrangementMARGAO: South Goa District Collector
visited Benabhat in Areal village on Tuesday evening to take stock of the ground situation
before directing the police and other authorities to stick to the alternate access for visitors to the statue of Shivaji Maharaj as agreed upon by the parties on Monday
After walking to the hilly terrain along with Additional Collector Srinet Kothwale and Velim MLA Cruz Silva
from the main road where the statue of Shivaji Maharaj was installed last year
the district collector went into a huddle with DySP Sidhant Shirodkar
and Salcete Mamlatdar Vimod Dalal to discuss the situation
She later told DySP Shirodkar that visitors who wanted to celebrate Shiv Jayanti on Wednesday should take the alternate access to the Shivaji statue
She assured the locals that the private property would not be used by the visitors to go to the statue
the collector further told DySP Shirodkar to deploy police at the site on Wednesday as a precautionary measure
Locals allege developer ‘stoking’ up tension for own gainsMARGAO: Sao Jose de Areal residents on Tuesday said they are neither against the statue of Shivaji Maharaj nor any religion and attributed the root of the tension to the development of plots in the area
Saying the people would never hurt the sentiments of anyone
who has been trying to develop the orchard land into plots since 2012
has stoked the controversy by giving a portion of this land to install the Shivaji statue last year
hoping it would provide road access to his developed plots
Peter Viegas told the media that for 10 years
the land developer Mehboob Makandkar has been trying to develop plots at Benabhat
has no access to his property due to the fields between his property and the main road
Tenant Milages Tereza told the media that he had issued an NOC to a party over a year ago to carry material to his tenanted field through misrepresentation
“The party had asked for an NOC to allow him to take material to his property
He misused the NOC to put the statue of Shivaji Maharaj
We are not against Shivaji Maharaj or any religion,” he added.