Interphase formation and degradation of charge transfer kinetics between a lithium metal anode and highly crystalline Li7P3S11 solid electrolyte

被引:401
作者
Wenzel, Sebastian [1 ]
Weber, Dominik A. [1 ]
Leichtweiss, Thomas [1 ]
Busche, Martin R. [1 ]
Sann, Joachim [1 ]
Janek, Juergen [1 ]
机构
[1] Univ Giessen, Inst Phys Chem, Heinrich Buff Ring 17, D-35392 Giessen, Germany
关键词
Li7P3S11; Solid state battery; SEI; Interphase formation; Lithium anode; In situ XPS; STATE LITHIUM; IONIC-CONDUCTIVITY; ELECTROCHEMICAL PROPERTIES; SUPERIONIC CONDUCTOR; BATTERY; LI10GEP2S12; DIFFUSION; CERAMICS; DYNAMICS; LIQUID;
D O I
10.1016/j.ssi.2015.11.034
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The properties of the interface between solid electrolytes and electrode materials are of vital importance for the performance of all solid-state batteries (ASSB). Unwanted reactions between alkali metal electrodes and the solid electrolyte can lead to the formation of compounds that either facilitate or block the ion transfer kinetics. In particular for lithium solid electrolytes in the Li2S-P2S5 system with very high lithium ion conductivity only little is known about interfacial reactions with lithium metal. Here we monitor the formation of an interphase between Li7P3S11 and lithium metal by a combined analytical approach, comprising in situ photoelectron spectroscopy and time-dependent electrochemical impedance spectroscopy. Utilizing a self -developed XPS peak fit model for Li7P3S11, we identify the components of this interphase, discuss its properties and develop a qualitative model, which shows that the reaction between electrolyte and lithium metal, and hence, the interphase growth, is limited to a few nm. The solid electrolyte being used is a highly crystalline form of the superionic conductor Li7P3S11 without any residual glassy phase, and the synthesis of this Li7P3S11 phase is also reported. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:24 / 33
页数:10
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