电化学
阳极
合金
材料科学
固态
冶金
化学工程
纳米技术
化学
电极
工程类
物理化学
作者
Won Joon Jeong,Congcheng Wang,Sun Geun Yoon,Yuhgene Liu,Timothy Chen,Matthew T. McDowell
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-05-08
卷期号:9 (6): 2554-2563
被引量:95
标识
DOI:10.1021/acsenergylett.4c00915
摘要
Lithium alloy anodes in the form of dense foils offer significant potential advantages over lithium metal and particulate alloy anodes for solid-state batteries (SSBs). However, the reaction and degradation mechanisms of dense alloy anodes remain largely unexplored. Here, we investigate the electrochemical lithiation/delithiation behavior of 12 elemental alloy anodes in SSBs with Li6PS5Cl solid-state electrolyte (SSE), enabling direct behavioral comparisons. The materials show highly divergent first-cycle Coulombic efficiency, ranging from 99.3% for indium to ∼20% for antimony. Through microstructural imaging and electrochemical testing, we identify lithium trapping within the foil during delithiation as the principal reason for low Coulombic efficiency in most materials. The exceptional Coulombic efficiency of indium is found to be due to unique delithiation reaction front morphology evolution in which the high-diffusivity LiIn phase remains at the SSE interface. This study links composition to reaction behavior for alloy anodes and thus provides guidance toward better SSBs.
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