电解质
X射线光电子能谱
阳极
离子电导率
电化学
电化学窗口
材料科学
锂(药物)
快离子导体
离子键合
电导率
化学工程
相间
离子
分析化学(期刊)
电极
化学
无机化学
物理化学
医学
有机化学
内分泌学
生物
工程类
遗传学
色谱法
作者
Sebastian Wenzel,Simon Randau,Thomas Leichtweiß,Dominik A. Weber,Joachim Sann,Wolfgang G. Zeier,Jürgen Janek
标识
DOI:10.1021/acs.chemmater.6b00610
摘要
The very high ionic conductivity of Li10GeP2S12 (LGPS) makes it a potential solid electrolyte for lithium all-solid-state batteries. Besides the high ionic conductivity, another key requirement is the stability of the solid electrolyte against degradation reactions with the electrodes; here, we analyze the reaction of LGPS with lithium metal. In situ X-ray photoelectron spectroscopy (XPS), in combination with time-resolved electrochemical measurements offers detailed information on the chemical reactions at the Li/LGPS interface. The decomposition of Li10GeP2S12 leads to the formation of an interphase composed of Li3P, Li2S, and Li–Ge alloy, which is in perfect agreement with theoretical predictions, and an increase of the interfacial resistance. These results highlight the necessity to perform long-term, time-resolved electrochemical measurements when evaluating potential new solid electrolytes for solid-state batteries. The kinetics of this interphase growth—comparable to SEI formation on lithium anodes in liquid electrolytes—seems to be governed by diffusion across the interphase, as a square root time dependence is observed.
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