镍
材料科学
降级(电信)
阴极
电解质
接口(物质)
化学工程
冶金
化学
电极
计算机科学
物理化学
复合材料
电信
毛细管数
毛细管作用
工程类
作者
Ye-Chao Wu,Feng Li,Xiao-Bin Cheng,Yi‐Hong Tan,Xin Huang,Jin‐Da Luo,Shu Chen,Ruijun Pan,Yi‐Chen Yin,Zheng Liang,Hong‐Bin Yao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-11-25
卷期号:24 (49): 15540-15546
被引量:4
标识
DOI:10.1021/acs.nanolett.4c03502
摘要
Despite competitive compatibility with high-nickel cathodes, chloride solid electrolytes (SEs) still experience inevitable side reactions at the cathode/SE interface, causing capacity decay in all-solid-state lithium batteries (ASSLBs) during cycling. Herein, a three-electrode ASSLB testing device is developed to comprehensively reveal the interface failure mechanisms of the ultrahigh-nickel LiNi0.92Co0.05Mn0.03O2 (NCM92) cathode paired with LaCl3-based chloride SE Li0.447La0.475Zr0.059Ta0.179Cl3 (LLZTC). Distribution of relaxation time (DRT) analysis clearly shows the ASSLB degradation accompanied by a significant NCM92/LLZTC interface impedance increase, which becomes more pronounced at the higher cutoff charging voltage of 4.8 V vs Li+/Li. Furthermore, time-of-flight secondary ion mass spectrometry (ToF-SIMS) and focused ion beam scanning electron microscopy (FIB-SEM) analysis also confirm the deterioration arising from active lattice oxygen and loss of physical contact at the NCM92/LLZTC interface. These findings reveal both electrochemical degradation and physical contact failure at the cathode/SE interface as key causes of the ASSLBs' capacity decay.
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