碱金属
降级(电信)
电解质
化学
无机化学
乙醚
相(物质)
化学工程
材料科学
有机化学
电极
计算机科学
电信
工程类
物理化学
作者
Xiaojuan Chen,Lei Qin,Jiaonan Sun,Songwei Zhang,Dan Xiao,Yiying Wu
标识
DOI:10.1002/anie.202207018
摘要
Abstract Localized high‐concentration electrolytes (LHCEs) have attracted interest in alkali metal batteries due to the advantages of forming stable solid‐electrolyte interphases (SEIs) on anodes and good chemical/electrochemical stability. Herein, a new degradation mechanism is revealed for ether‐based LHCEs that questions their compatibility with alkali metal anodes (Li, Na, and K). Specifically, the ether solvent reacts with alkali metals to generate solvated electrons (e s − ) that attack hydrofluoroether co‐solvents to form a series of byproducts. The ether solvent essentially acts as a phase‐transfer reagent that continuously transfers electrons from solid‐phase metals into the solution phase, thus inhibiting the formation of stable SEI and leading to continuous alkali metal corrosion. Switching to an ester‐based solvating solvent or intercalation anodes such as graphite or molybdenum disulfide has been shown to avoid such a degradation mechanism due to the absence of e s − .
科研通智能强力驱动
Strongly Powered by AbleSci AI