阴极
材料科学
离子电导率
活化能
电导率
离子键合
电池(电)
相间
热传导
涂层
化学工程
纳米技术
化学物理
离子
电解质
化学
电极
物理化学
复合材料
热力学
功率(物理)
物理
生物
有机化学
工程类
遗传学
作者
Pushun Lu,Sheng Gong,Chuhong Wang,Zhiao Yu,Yuli Huang,Tenghuan Ma,Jingchen Lian,Zhiwen Jiang,Liquan Chen,Hong Li,Fan Wu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-02-29
卷期号:18 (10): 7334-7345
被引量:20
标识
DOI:10.1021/acsnano.3c07023
摘要
All-solid-state batteries (ASSBs) working at room and mild temperature have demonstrated inspiring performances over recent years. However, the kinetic attributes of the interface applicable to the subzero temperatures are still unidentified, restricting the low-temperature interface design and operation. Herein, a host of cathode interfaces are constructed and investigated to unlock the critical interface features required for cryogenic temperatures. The unstable interface between LiNi0.90Co0.05Mn0.05O2 (Ni90) and Li6PS5Cl (LPSC) sulfide solid electrolyte (SE) results in unfavorable cathode–electrolyte interphase (CEI) and sluggish lithium-ion transport across the CEI. After inserting a Li2ZrO3 (LZO) coating layer, the activation energy of the Ni90@LZO/sulfide SE interface can be reduced from 60.19 kJ mol–1 to 41.39 kJ mol–1 owing to the suppressed interfacial reactions. Through replacing the LPSC SE and LZO coating layer by the Li3InCl6 (LIC) halide SE, both a highly stable interface and low activation energy (25.79 kJ mol–1) can be achieved, thus realizing an improved capacity retention (26.9%) at −30 °C for the Ni90/LIC/LPSC/Li-In ASSB. Moreover, theoretical evaluation clarifies that cathode/SE interfaces with high ionic conductivity and low energy barrier are favorable to the Li+ conduction through the interphase and the Li+ transfer across the cathode/interphase interface. These critical understandings may provide guidance for low-temperature interface design in ASSBs.
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