Deciphering Chemical/Electrochemical Compatibility of Li3InCl6 in 5.2 V High-Voltage LiCoO2 All-Solid-State Batteries

被引:4
|
作者
Wang, Zhen [1 ]
Tan, Jiewen [1 ]
Jia, Zhanhui [2 ]
Cui, Jiawu [1 ]
Wang, Xiaowei [4 ]
Shu, Chengyong [1 ]
Gao, Xiangwen [5 ]
Wu, Yuping [3 ]
Tang, Wei [1 ]
机构
[1] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, Xian 710049, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Mat Sci & Engn, Xian 710049, Peoples R China
[3] Southeast Univ, Sch Energy & Environm, Nanjing 210096, Peoples R China
[4] Argonne Natl Lab, Chem Sci & Engn Div, Lemont, IL 60439 USA
[5] Shanghai Jiao Tong Univ, Global Inst Future Technol, Future Battery Res Ctr, Shanghai 200240, Peoples R China
来源
ACS ENERGY LETTERS | 2024年 / 9卷 / 09期
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
ELECTROLYTE; CONDUCTORS; CAPACITY; PROGRESS;
D O I
10.1021/acsenergylett.4c01472
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Large interfacial resistance is a widely recognized impediment to the advancement of high-voltage, all-solid-state batteries. However, a comprehensive understanding of the fundamental cause behind the interfacial resistance between solid electrolytes and typical layered oxide cathodes has not yet been achieved. Here, we investigated the high-voltage stability of Li3InCl6 and elucidated the underlying interfacial electrochemical reactions between LiCoO2 and Li3InCl6. The pairing of Li3InCl6 with LiCoO2 exhibited a superior capacity retention of 73.6% even at 5.2 V, much higher than 28.2% charged at 4.6 V in lithium-ion batteries after 70 cycles. The enhanced high-voltage stability of ASSBs is attributed to the stable interface formed between LiCoO2 and Li3InCl6 and the reinforced surface and bulk structure stability. On the other hand, the ultrahigh voltage still causes the partial decomposition of Li3InCl6 and generates interfacial compounds such as InClO and cobalt and indium chlorides/oxides.
引用
收藏
页码:4485 / 4492
页数:8
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