Electrochemistry
Online ISSN : 2186-2451
Print ISSN : 1344-3542
ISSN-L : 1344-3542
Articles
Kinetics of Interfacial Lithium-ion Transfer between a Graphite Negative Electrode and a Li2S-P2S5 Glassy Solid Electrolyte
Danni YUMeiqi HUANGYuto MIYAHARAKohei MIYAZAKI Akitoshi HAYASHIMasahiro TATSUMISAGOTakeshi ABETomokazu FUKUTSUKA
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2022 Volume 90 Issue 3 Pages 037003

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Abstract

All-solid-state lithium-ion batteries that use sulfide solid electrolytes have attracted much attention due to their high safety and wide electrochemical window. In this study, highly oriented pyrolytic graphite (HOPG) and 75Li2S-25P2S5 (mol%) glass were used as a model graphite negative electrode and a sulfide solid electrolyte, respectively. Interfacial lithium-ion transfer between 75Li2S-25P2S5 glass and the HOPG electrode was studied by AC impedance spectroscopy measurements. The activation energy of the interfacial lithium-ion transfer was estimated to be around 37 kJ mol−1, which was much smaller than that at the interface between organic liquid electrolytes and HOPG electrode, indicating that the lithium-ion transfer at the interface between 75Li2S-25P2S5 glass and HOPG electrode proceeded quite rapidly. Furthermore, surface deposition of TiO2 and surface oxidation on HOPG electrodes were performed using the atomic layer deposition (ALD) method. Interfacial lithium-ion transfer between 75Li2S-25P2S5 glass and ALD-modified-HOPG electrodes was also investigated. The activation energies of the interfacial lithium-ion transfer were slightly higher than that of HOPG, but the resistance of the charge-transfer process was lower, indicating that the affinity of the HOPG electrode for the glass electrolyte was improved by surface modification.

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© The Author(s) 2021. Published by ECSJ.

This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium provided the original work is properly cited. [DOI: 10.5796/electrochemistry.21-00127].
http://creativecommons.org/licenses/by/4.0/
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