Journal
ELECTROCHEMISTRY
Volume 80, Issue 10, Pages 740-742Publisher
ELECTROCHEMICAL SOC JAPAN
DOI: 10.5796/electrochemistry.80.740
Keywords
Lithium Secondary Battery; All-Solid-State Battery; Sulfide Solid Electrolyte; Microelectrode
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Funding
- Japan Science and Technology Agency (JST), Core Research for Evolutional Science and Technology (CREST) project
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Charge transfer kinetics at the Li metal electrode/electrolyte interface for three inorganic solid electrolytes and an organic liquid electrolyte were elucidated with two parameters, exchange current density (i(0)) for Li/Li+ couple reactions and ionic conductivity in electrolyte. The former was evaluated by potential step method with a microelectrode, while the latter was done by electrochemical impedance spectroscopy. Both i(0) and ionic conductivity showed Arrhenius type dependence, and activation energies (E-a) for the charge transfer reactions and ionic conduction were evaluated. In the case of the organic liquid electrolyte, E-a for the Li/Li+ couple reactions was higher than that for ionic conduction because of the solvation/desolvation of Li+ ion. However, for the Li2S-P2S5 solid solid electrolytes, the E-a for the Li/Li+ couple reactions was quite close to that for ionic conduction due to the lack of the solvation/desolvation. (C) The Electrochemical Society of Japan, All rights reserved.
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