电解质
相间
阳极
锂(药物)
金属
材料科学
离子
电极
金属锂
自行车
化学工程
化学
无机化学
冶金
物理化学
有机化学
生物
历史
工程类
内分泌学
考古
医学
遗传学
作者
Hansen Wang,William Huang,Zhiao Yu,Wenxiao Huang,Rong Xu,Zewen Zhang,Zhenan Bao,Yi Cui
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-02-03
卷期号:6 (2): 816-825
被引量:52
标识
DOI:10.1021/acsenergylett.0c02533
摘要
Advanced electrolytes were developed to improve the cyclability of lithium (Li) metal anodes, yet their working mechanisms remain unclear. Here, we study the Li cycling performance under different pressures in a 1 M Li bis(fluorosulfonyl)imide/fluorinated 1,4-dimethoxybutane electrolyte. A consistently long cycle life is achieved over a wide range of pressures (30–600 psi). This is due to a completely different Li plating mode with more favorable deposition morphologies compared to that in a conventional carbonate electrolyte, which exhibits increasing cycle stability with increased pressure. We show that this is enabled by the properties of an anion-derived residual solid-electrolyte interphase (rSEI) framework on the electrode surface, an undercharacterized structure with profound implications for Li metal cycling. This anion-derived rSEI chemistry is likely the key to a prolonged cycle life of Li metal batteries and should be vigorously addressed in future electrolyte designs.
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