Synergistical coupling Janus SnS-Fe1-xS heterostructure cell and polydopamine-derived S doped carbon as high-rate anodes for sodium-ion batteries

被引:36
作者
Zhao, Fengjun [1 ]
Xiao, Xinyu [1 ]
Yang, Linyu [2 ]
Wang, Zhen [1 ]
Xu, Shurong [1 ]
Liu, Jun [1 ]
机构
[1] Cent South Univ, Sch Mat Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Xinjiang Univ, Sch Mat Sci & Engn, Urumqi 830000, Xinjiang Uygur, Peoples R China
关键词
Sodium-ion batteries; Bimetallic sulfides; Heterostructure cell; Janus nanoarchitecture; HIGH-PERFORMANCE ANODE; YOLK-SHELL STRUCTURE; ENERGY-STORAGE; ELECTROCHEMICAL PERFORMANCE; METAL SULFIDE; SNS; NANOSPHERES; NANOSHEETS; NITROGEN; LITHIUM;
D O I
10.1016/j.cej.2021.130534
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
As a potential anode material for sodium-ion batteries, tin sulfide (SnS) has been widely studied. However, sluggish kinetics, severe volume variation, and poor rate performance during cycling greatly hindered its application. Herein, a facile coprecipitation method combining with the carbon coated route and sulfuration process is designed to synthesize a novel SFS@SC nanocube. Unlike previous reports of bimetallic sulfides for sodium-ion batteries, the nanocubes exhibit a nanostructure with heterogeneous SnS/Fe1-xS distribution instead of the aggregation, resembling the double-faced god Janus, and each nanocube could be regarded as a Janus SnSFe1-xS heterostructure cell. Owing to the delicate Janus nanoarchitecture with enhanced charge transfer, the SFS@SC exhibits good cycling stability and rate property. In particular, the SFS@SC electrode delivers a high specific capacity of 610 mAh g(-1) after 150 cycles at a current density of 0.1 A g(-1), and a long cycle life with a capacity of 310 mAh g(-1) after 2900 cycles at 2.0 A g(-1).
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页数:9
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