纳米片
电解质
相间
材料科学
阴极
电极
锂(药物)
化学工程
原位
离子
纳米技术
化学
工程类
物理化学
医学
有机化学
生物
内分泌学
遗传学
作者
Qingyong Zhang,Jiale Ma,Liang Mei,Jun Liu,Zhenyu Li,Li Ju,Zhiyuan Zeng
出处
期刊:Matter
[Elsevier]
日期:2022-04-01
卷期号:5 (4): 1235-1250
被引量:52
标识
DOI:10.1016/j.matt.2022.01.015
摘要
Summary
The formation behaviors of LiF nanocrystals have been studied on anodes in Li-ion batteries; there is no research work reporting LiF crystal growth on cathodes. Here, we report a real-time LiF crystal formation on positively charged titanium (Ti) electrodes in an electrochemical liquid cell with 150-nm-thick Li hexafluorophosphate (LiPF6)/propylene carbonate (PC) liquid electrolyte loaded. The LiF nanocrystals show two-dimensional (2D) morphologies on the electrode surface, which can serve as a cathode electrolyte interface (CEI). Furthermore, the merging of LiF nanosheets was also observed, which may underlie the self-healing ability of LiF-based CEIs. Theoretical modeling indicates that there are two types of LiF formation paths on positive voltage-biased Ti electrodes. This work shows the remarkable morphing mobility and self-healing ability of LiF nanosheets and sheds light on strategies of modulating LiF nanocrystals and cathode surface chemistry for improving battery performance and cycle life.
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