Encapsulating Co9S8 nanocrystals into CNT-reinforced N-doped carbon nanofibers as a chainmail-like electrocatalyst for advanced Li-S batteries with high sulfur loading

被引:61
作者
Liu, Jintao [1 ]
Xiao, Shuhao [1 ]
Liu, Xingquan [1 ]
Wu, Rui [1 ]
Niu, Xiaobin [1 ]
Xiang, Yong [1 ]
Chen, Jun Song [1 ]
Yang, Chenghao [2 ]
机构
[1] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 610054, Peoples R China
[2] South China Univ Technol, Sch Environm & Energy, New Energy Res Inst, Guangzhou Key Lab Surface Chem Energy Mat, Guangzhou 510006, Peoples R China
基金
中国国家自然科学基金;
关键词
Co9S8; nanocrystals; Chainmail-like electrocatalyst; First-principle calculations; Li-S batteries; High sulfur loading; POROUS CARBON; PERFORMANCE; METAL; NANOTUBES; CO; CONVERSION; ELECTRODE; EVOLUTION; CATHODE; SHELL;
D O I
10.1016/j.cej.2021.130246
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Li-S batteries have been regarded as one promising candidate for next-generation energy storage systems, however, their practical implementations are severely hindered by the intractable polysulfides shuttle (PSS) effect and retarded conversion kinetics. Herein, a flexible electrode consisting of Co9S8 nanocrystals and CNTs encapsulated inside porous N-doped carbon nanofibers (NCF) (CNT@NC/Co9S8) was developed by electrospinning followed by in-situ sulfurization. The carbon nanofibers and embedded CNTs build a highly conductive network, while the Co9S8 and N dopant provide more polar sites for LiPSs confinement. This self-supported flexible electrode with a sulfur loading of 12.5 mg cm(-2) exhibits a high initial discharge capacity (1207.7 mAh g(-1) at 0.1C), excellent rate capability (831.2 mAh g(-1) at 4.0C) and cycling stability (765.5 mAh g(-1) with a capacity retention of 78.1% after 1000 cycles at 2.0C). Moreover, when the sulfur loading increases to 20 and 30 mg cm(-2), high capacities of 869.2 and 706.6 mAh g(-1) can still be obtained at 0.1C after 100 cycles, respectively. Theoretical analysis suggests that the sulfur cathode built on CNT@NC/Co9S8 is electrocatalytically active towards LiPSs redox with enhanced conversion dynamics, thus mitigating the detrimental PSS effect.
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页数:11
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