Oriented outperforms disorder: Thickness-independent mass transport for lithium-sulfur batteries

被引:14
作者
Fan, Xia-Lu [1 ,2 ]
Ping, Lin-Quan [1 ,2 ]
Qi, Fu-Lai [1 ]
Ghazi, Zahid Ali [1 ]
Tang, Xiao-Nan [3 ]
Fang, Ruo-Pian [4 ]
Sun, Zhen-Hua [1 ]
Cheng, Hui-Ming [1 ,5 ]
Liu, Chang [1 ]
Li, Feng [1 ]
机构
[1] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Liaoning, Peoples R China
[2] Univ Sci & Technol China, Sch Mat Sci & Engn, Hefei 230026, Anhui, Peoples R China
[3] Shandong Univ Technol, Sch Chem Engn, Zibo 255049, Peoples R China
[4] Univ New South Wales, Sch Chem Engn, Sydney, NSW 2033, Australia
[5] Tsinghua Univ, TBSI, Shenzhen Geim Graphene Ctr, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
CARBON NANOTUBE HYBRIDS; POROUS CARBON; PERFORMANCE; GRAPHENE; CATHODE; ENERGY; ELECTRODES; RESERVOIR; CAPACITY; ANODE;
D O I
10.1016/j.carbon.2019.07.087
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
Extreme fast charging in a thick electrode film is critical for high rate lithium sulfur batteries. However, the high ion-path tortuosity of most carbon/sulfur cathodes dramatically hinder their mass transport, thus leading to poor rate performance. This situation goes worse with increasing the electrode thickness. Here, we report a binder-free vertically-aligned carbon nanotube/sulfur (VACNT/S) cathode with an excellent thickness-independent mass transport and high-rate performance. Compared with a conventional disordered carbon nanotube/sulfur electrode, the highly conductive VACNTs provide directional paths for the ultrafast transfer of both lithium ions and electrons, leading to improved kinetics and a stable redox activity. The VACNT/S electrode shows an extremely high initial specific capacity of 894 mA h g(-1)at a 5 C rate, and very stable charge/discharge performance with a capacity of 486.1 mA h g(-1) after 400 cycles and a low capacity decay rate of 0.1% per cycle. This work demonstrates an efficient pathway for the design of electrodes for high-rate lithium sulfur batteries. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:90 / 97
页数:8
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