In-situ CNT-loaded organic cathodes for sulfide all-solid-state Li metal batteries

被引:5
作者
Song, Fengmei
Wang, Zhixuan [1 ,2 ,3 ]
Sun, Guochen [3 ]
Ma, Tenghuan [1 ,5 ]
Wu, Dengxu [1 ,2 ,3 ,4 ]
Chen, Liquan [1 ,2 ,3 ,4 ]
Li, Hong [1 ,2 ,3 ,4 ]
Wu, Fan [1 ,2 ,3 ,4 ,5 ]
机构
[1] Tianmu Lake Inst Adv Energy Storage Technol, Liyang 213300, Jiangsu, Peoples R China
[2] Yangtze River Delta Phys Res Ctr, Liyang 213300, Jiangsu, Peoples R China
[3] Chinese Acad Sci, Inst Phys, Beijing Adv Innovat Ctr Mat Genome Engn, Key Lab Renewable Energy, Beijing 100190, Peoples R China
[4] Univ Chinese Acad Sci, Sch Phys Sci, Beijing 100049, Peoples R China
[5] Univ Sci & Technol China, Nano Sci & Technol Inst, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
All-solid-state batteries; Organic electrode materials; Sulfide solid electrolytes; Lithium batteries; Carbon nanotubes; In-situ interfacial engineering; COMPOSITE ELECTRODE; LI6PS5X X; LITHIUM; DESIGN; REDOX; BR; CL;
D O I
10.1016/j.etran.2023.100261
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Organic cathodes show promising advantages of extensive resources, high theoretical specific capacity, and mild synthesis conditions, etc., but suffer from low density, poor electronic conductivity, and high solubility in liquid electrolytes. Herein, an in-situ coating method is developed to overcome the above issues by realizing highperformance sulfide all-solid-state batteries with organic Li4C8H2O6 cathode. Li4C8H2O6 composite cathodes with carbon nanotubes (CNTs) and vapor grown carbon fiber (VGCF) were systematically studied to reveal that CNTs accelerate the electrochemical decomposition of sulfide electrolyte, despite the effectively improved electronic conductivity, rate capability and active material utilization. Therefore, in-situ coating of Li4C8H2O6 onto CNTs (Li4C8H2O6@CNT) is developed to further improve the contact between Li4C8H2O6 and CNTs, but to reduce the contact of CNTs with sulfide solid electrolyte and its decomposition. As a result, the Li4C8H2O6@CNT electrode demonstrates a high capacity of 200.3 mAh/g, and a high active material utilization rate (83.4% at 0.1C). It also exhibits a specific capacity of 85.9 mAh/g at a high cathode loading of 40 wt% and a high rate of 1C.
引用
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页数:8
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