法拉第效率
材料科学
电解质
阳极
钝化
电化学
锂(药物)
图层(电子)
化学工程
金属
电极
纳米技术
化学
冶金
物理化学
医学
内分泌学
工程类
作者
Zachary D. Hood,Xi Chen,Robert L. Sacci,Xiaoming Liu,Gabriel M. Veith,Yifei Mo,Junjie Niu,Nancy J. Dudney,Miaofang Chi
出处
期刊:Nano Letters
[American Chemical Society]
日期:2020-12-18
卷期号:21 (1): 151-157
被引量:58
标识
DOI:10.1021/acs.nanolett.0c03438
摘要
Li phosphorus oxynitride (LiPON) is one of a very few solid electrolytes that have demonstrated high stability against Li metal and extended cyclability with high Coulombic efficiency for all solid-state batteries (ASSBs). However, theoretical calculations show that LiPON reacts with Li metal. Here, we utilize in situ electron microscopy to observe the dynamic evolutions at the LiPON–Li interface upon contacting and under biasing. We reveal that a thin interface layer (~60 nm) develops at the LiPON–Li interface upon contact. This layer is composed of conductive binary compounds that show a unique spatial distribution that warrants an electrochemical stability of the interface, serving as an effective passivation layer. Our results explicate the excellent cyclability of LiPON and reconcile the existing debates regarding the stability of the LiPON–Li interface, demonstrating that, though glassy solid electrolytes may not have a perfect initial electrochemical window with Li metal, they may excel in future applications for ASSBs.
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