电解质
二聚体
电化学
石英晶体微天平
乙醚
化学
阳极
化学工程
电极
无机化学
材料科学
有机化学
吸附
溶剂
物理化学
工程类
作者
Jun Pan,Yi‐Yang Sun,Yehao Yan,Lei Feng,Yifan Zhang,Aming Lin,Fuqiang Huang,Jian Yang
出处
期刊:JACS Au
[American Chemical Society]
日期:2021-07-06
卷期号:1 (8): 1208-1216
被引量:48
标识
DOI:10.1021/jacsau.1c00158
摘要
Hard carbons (HCs) as an anode material in sodium ion batteries present enhanced electrochemical performances in ether-based electrolytes, giving them potential for use in practical applications. However, the underlying mechanism behind the excellent performances is still in question. Here, ex situ nuclear magnetic resonance, gas chromatography-mass spectrometry, and high-resolution transmission electron microscopy were used to clarify the insightful chemistry of ether- and ester-based electrolytes in terms of the solid-electrolyte interphase (SEI) on hard carbons. The results confirm the marked electrolyte decomposition and the formation of a SEI film in EC/DEC but no SEI film in the case of diglyme. In situ electrochemical quartz crystal microbalance and molecular dynamics support that ether molecules have likely been co-intercalated into hard carbons. To our knowledge, these results are reported for the first time. It might be very useful for the rational design of advanced electrode materials based on HCs in the future.
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