材料科学
阳极
过电位
电极
介电谱
极化(电化学)
电化学
动力学
化学工程
硫化物
降级(电信)
自行车
原位
分析化学(期刊)
电池(电)
电化学电池
硫化钴
电阻抗
放松(心理学)
衰退
电化学动力学
作者
Ruizhuo Zhang,Aleksandr Kondrakov,Jürgen Janek,Torsten Brezesinski
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-12-18
卷期号:20 (1): 1225-1237
被引量:2
标识
DOI:10.1021/acsnano.5c17276
摘要
Solid-state batteries (SSBs) are primarily tested in two-electrode and/or symmetric cell configurations, which may lead to under- or overestimation of degradation and failure. For long-term cycling and under dynamic conditions, the contribution of the counter electrode (anode) to fading may be substantial but is rarely reported due to lack of suitable characterization techniques. Here, we employed an advanced three-electrode cell setup to elucidate the overpotential growth and interface-related kinetic response for commonly used counter electrodes in lab-scale testing, namely, Li4Ti5O12 and In/InLi, as well as for LiNbO3-coated LiNi0.85Co0.10Mn0.05O2 as the working electrode (cathode) in thiophosphate-based SSB cells. This was achieved through continuous monitoring of individual electrode potentials (>1500 h) and by performing electrochemical impedance spectroscopy measurements in situ in combination with distribution of relaxation times analysis. The results reveal distinct differences in polarization and interfacial kinetics between the Li4Ti5O12 and In/InLi anodes in practical application scenarios and how these affect cyclability and the analysis of capacity fading.
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