Strongly coupled metal-organic frameworks on layered bimetallic hydroxide derived N, S Co-doped porous carbon frameworks embedding with CoS2 for energy storage

被引:50
|
作者
Wang, Junling [1 ]
Han, Longfei [1 ]
Wu, Na [1 ]
Zhang, Zixuan [1 ]
Liao, Can [1 ]
Wang, Jingwen [1 ]
Kan, Yongchun [1 ]
Hu, Yuan [1 ]
机构
[1] Univ Sci & Technol China, State Key Lab Fire Sci, CAS Key Lab Soft Matter Chem, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium storage performance; Sodium storage performance; Supercapacitor; Transition metal chalcogenides; Pseudocapacitive contribution; HIGH-PERFORMANCE ANODE; REDUCED GRAPHENE OXIDE; SODIUM-ION BATTERY; IMPROVED ELECTROCHEMICAL PERFORMANCE; LITHIUM-ION; HIGH-CAPACITY; RATE CAPABILITY; OXYGEN REDUCTION; RATIONAL DESIGN; NANOSHEETS;
D O I
10.1016/j.jpowsour.2020.227789
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
In this work, we propose the fabrication of N, S co-doped carbon framework with confined CoS2 nanoparticles and rooted carbon nanotubes (NSPCF@CoS2). As LIBs anode, the NSPCF@CoS2 electrode gives an inceptive discharge capacity of 921.5 mA h g(-1), with Coulombic efficiency of above 97% during the 200 cycles (except for the previous 5 cycles). As SIBs anode (the applied voltage range is 0.4-3 V), the NSPCF@CoS2 electrode performs a steady and relatively high capacity (over 448.0 mA h g(-1)) during the 1650 cycles, and an extremely low capacity decay rate of 0.018% per cycle is obtained. Also, the NSPCF@CoS2 electrode shows a high capacity of 545.3 mA h g(-1) even at 8 A g(-1) (the applied voltage range is 0.1-3 V). This NSPCF@CoS2 electrode shows a comparable or even higher rate performance than many reported transition metal chalcogenides materials, confirming its promising usage. The presence of pseudocapacitive contribution is verified, after the deep investigation on Li+/Na+ storage behavior and reaction kinetics. In addition, this rationally designed structure gives potential application in supercapacitor.
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页数:11
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