Microelectrode Studies on Kinetics of Charge Transfer at an Interface of Li Metal and Li2S-P2S5 Solid Electrolytes

被引:21
作者
Chiku, Masanobu [1 ]
Tsujiwaki, Wataru [1 ]
Higuchi, Eiji [1 ]
Inoue, Hiroshi [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Sakai, Osaka 5998531, Japan
基金
日本科学技术振兴机构;
关键词
Lithium Secondary Battery; All-Solid-State Battery; Sulfide Solid Electrolyte; Microelectrode; LITHIUM; BATTERY; ANODE;
D O I
10.5796/electrochemistry.80.740
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
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.
引用
收藏
页码:740 / 742
页数:3
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