石墨
材料科学
插层(化学)
拉曼光谱
锂(药物)
电解质
离子键合
金属
电化学
成核
快离子导体
化学工程
无机化学
化学物理
化学
物理化学
离子
复合材料
电极
冶金
有机化学
工程类
医学
物理
光学
内分泌学
作者
Daxian Cao,Yuxuan Zhang,Tongtai Ji,Xianhui Zhao,Ercan Cakmak,Soydan Ozcan,Michael Geiwitz,Jean-Christophe Bilheux,Kang Xu,Ying Wang,Kenneth S. Burch,Qingsong Tu,Hongli Zhu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-01-25
卷期号:24 (5): 1544-1552
被引量:2
标识
DOI:10.1021/acs.nanolett.3c04072
摘要
Lithium–metal (Li0) anodes potentially enable all-solid-state batteries with high energy density. However, it shows incompatibility with sulfide solid-state electrolytes (SEs). One strategy is introducing an interlayer, generally made of a mixed ionic-electronic conductor (MIEC). Yet, how Li behaves within MIEC remains unknown. Herein, we investigated the Li dynamics in a graphite interlayer, a typical MIEC, by using operando neutron imaging and Raman spectroscopy. This study revealed that intercalation-extrusion-dominated mechanochemical reactions during cell assembly transform the graphite into a Li-graphite interlayer consisting of SE, Li0, and graphite-intercalation compounds. During charging, Li+ preferentially deposited at the Li-graphite|SE interface. Upon further plating, Li0-dendrites formed, inducing short circuits and the reverse migration of Li0. Modeling indicates the interface has the lowest nucleation barrier, governing lithium transport paths. Our study elucidates intricate mechano-chemo-electrochemical processes in mixed conducting interlayers. The behavior of Li+ and Li0 in the interlayer is governed by multiple competing factors.
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