Supersaturated bridge-sulfur and vanadium co-doped MoS2 nanosheet arrays with enhanced sodium storage capability

被引:47
|
作者
Dong, Yuru [1 ]
Zhu, Zhengju [1 ]
Hu, Yanjie [1 ]
He, Guanjie [2 ]
Sun, Yue [1 ]
Cheng, Qilin [1 ]
Parkin, Ivan P. [2 ]
Jiang, Hao [1 ]
机构
[1] East China Univ Sci & Technol, Shanghai Engn Res Ctr Hierarch Nanomat, Sch Mat Sci & Engn, Key Lab Ultrafine Mat,Minist Educ, Shanghai 200237, Peoples R China
[2] UCL, Dept Chem, Christopher Ingold Lab, 20 Gordon St, London WC1H 0AJ, England
基金
中国国家自然科学基金;
关键词
MoS2; bridge-sulfur; high specific capacity; sodium-ion battery; cycle life; ION BATTERIES; GRAPHENE; LITHIUM; NANOFLOWERS; EVOLUTION;
D O I
10.1007/s12274-020-3044-x
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
The low specific capacity and sluggish electrochemical reaction kinetics greatly block the development of sodium-ion batteries (SIBs). New high-performance electrode materials will enhance development and are urgently required for SIBs. Herein, we report the preparation of supersaturated bridge-sulfur and vanadium co-doped MoS(2)nanosheet arrays on carbon cloth (denoted as V-MoS2+x/CC). The bridge-sulfur in MoS(2)has been created as a new active site for greater Na(+)storage. The vanadium doping increases the density of carriers and facilitates accelerated electron transfer. The synergistic dual-doping effects endow the V-MoS2+x/CC anodes with high sodium storage performance. The optimized V-MoS2.49/CC gives superhigh capacities of 370 and 214 mAh.g(-1)at 0.1 and 10 A.g(-1)within 0.4-3.0 V, respectively. After cycling 3,000 times at 2 A.g(-1), almost 83% of the reversible capacity is maintained. The findings indicate that the electrochemical performances of metal sulfides can be further improved by edge-engineering and lattice-doping co-modification concept.
引用
收藏
页码:74 / 80
页数:7
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