电化学
电解质
阴极
固态
材料科学
接口(物质)
纳米技术
化学工程
工程物理
化学
电极
工程类
物理化学
复合材料
毛细管数
毛细管作用
作者
Patrick Kwon,Carlos Juarez‐Yescas,Hyewon Jeong,Saeed Moradi,Elizabeth Gao,Debbie Lawrence,Beniamin Zahiri,Paul V. Braun
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-09-05
卷期号:9 (10): 4746-4752
被引量:12
标识
DOI:10.1021/acsenergylett.4c02062
摘要
The stability of the interface between the cathode and the solid electrolyte (SE) has been found to be a key determinant of solid-state battery (SSB) performance. While interfacial failure from electrochemical cycling has been studied, temperature effects on the chemical and electrochemical evolution of interface properties are not well-understood. We utilize a dense additive-free LiCoO2 cathode, which provides controlled morphology and crystallography, and well-known high voltage halide SEs (Li3InCl6 and Li3YCl6) to eliminate the need for cathode coating to explore the nature of interface deterioration induced by operating at up to 100 °C. By promoting temperature-induced accelerated interfacial failure, we show that at elevated temperatures (>60 °C) and higher states of charge, a significant chemo-electrochemical contribution to interfacial resistance results in rapid cell performance degradation. Our findings show that beyond the well sought-after SE electrochemical voltage stability, the atomic-scale restructuring of the cathode surface interfaced with the SE must be considered when designing stable interfaces.
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