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Space Science Digital > Blog > Technology > 3D internal structure of rechargeable batteries revealed for the first time
Technology

3D internal structure of rechargeable batteries revealed for the first time

By Aimee Daly March 13, 2023 4 Min Read
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Graphite crystal model sample and SEI formation on the edge section vs basal plane. a Optical image of a cross-section HOPG model sample. b Raman spectra at polished section and basal plane of as-prepared model sample. c First two cyclic voltammetry (CV) curves of model sample. (0.5 mV/s scan rate, 1 M LiPF6 salt in the EC/DMC = 1:1 vol% electrolyte) (d) G band of operando Raman spectra at section area upon the first lithium intercalation. e–h Dynamic topography evolutions during the 1st CV scan in ethylene carbonate (EC) based electrolyte, high magnification atomic force microscopy (AFM) images of SEI formation on sample (g) edge planes and h basal planes. i, j Cross-section profiles and schematics of the graphite atomic step wrapping in (h) at different voltage ranges 1 and 6, correspondingly. Credit: Nature Communications (2023). DOI: 10.1038/s41467-023-37033-7

Lancaster University researchers have pioneered a technique to observe the 3D internal structure of rechargeable batteries for the first time.

The research, published in Nature Communications, is led by Professor Oleg Kolosov from Lancaster’s Physics Department in collaboration with University College London and NEXGENNA Faraday Institution Consortium.

The team used a novel 3D Nano-Rheology Microscopy (3DNRM) -based technique to visualize the 3D nanostructure inside rechargeable batteries, from the molecular scale electrical double-layer to the nanoscale-thick electrochemical surface layer on the graphite anode surface in a lithium-ion battery.

For the first time, this enabled the direct observation of the progression of the whole three dimensional structure of the solid electric interface (SEI), a nanoscale passivation layer formed on the battery electrode-electrolyte interface, that predetermines key battery properties.

The authors were able to reveal key predictors of SEI layer formation in a complex interplay of molecular dimension electrical double layer structures, surface properties of carbon layers and solvent—Li ions interaction in the electrolyte.

The nanoarchitecture of solid-liquid interfaces are critical for high performance batteries, but it has been difficult to characterize reaction interfaces within batteries due to their inherent inaccessibility.

Dr. Yue Chen of Lancaster University, who is the lead author, said, “So far, understanding the SEI formation mechanism is still a most challenging and least explored area due to the lack of an interfacial characterization technique capable of both nanoscale resolution and operation in the working battery environment.”

The dynamics of interfacial reactions define energy flow and conversion and govern chemical species transfer in important physical, chemical and biological processes, from catalytic reactions, energy storage and release in batteries, to antigen-antibody interactions and information transmission across neural cells.

This opens up a wide range of areas for the new technique from energy storage and chemical engineering to biomedical applications.

More information:
Chen, Y. et al, Nanoarchitecture factors of solid electrolyte interphase formation via 3D nano-rheology microscopy and surface force-distance spectroscopy, Nature Communications (2023). DOI: 10.1038/s41467-023-37033-7. www.nature.com/articles/s41467-023-37033-7

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Lancaster University


Citation:
3D internal structure of rechargeable batteries revealed for the first time (2023, March 13)
retrieved 13 March 2023
from https://phys.org/news/2023-03-3d-internal-rechargeable-batteries-revealed.html

This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
part may be reproduced without the written permission. The content is provided for information purposes only.



TAGGED: batteries, internal, rechargeable, revealed, structure, time

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