Constructing MoS2-SnS heterostructures on N-doped carbon nanosheets for enhanced catalytic conversion of polysulfides in lithium-sulfur batteries

被引:30
|
作者
Zhang, Junpu [1 ]
Xi, Wen [1 ]
Yu, Feng [1 ]
Zhang, Youfang [2 ]
Wang, Rui [1 ]
Gong, Yansheng [1 ]
He, Beibei [1 ]
Wang, Huanwen [1 ]
Jin, Jun [1 ,3 ]
机构
[1] China Univ Geosci, Fac Mat Sci & Chem, Wuhan 430074, Peoples R China
[2] Hubei Univ, Sch Mat Sci & Engn, Hubei Key Lab Polymer Mat, Minist Educ Key Lab Green Preparat & Applicat Func, Wuhan 430062, Peoples R China
[3] China Univ Geosci, Shenzhen Res Inst, Shenzhen 518000, Peoples R China
基金
中国国家自然科学基金;
关键词
Li -S batteries; MoS 2-SnS/NC heterostructure; Separator modification; Strong adsorption; Fast conversion; NITROGEN; ADSORPTION; SEPARATOR; NANOSPHERES; MEDIATOR; REDOX; ANODE;
D O I
10.1016/j.cej.2023.146009
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Lithium-sulfur (Li-S) batteries have been regarded as potential candidates for next-generation high-performance energy storage systems due to the rich sulfur reserves, nontoxicity, high theoretical capacity, and energy density. However, the Li-S batteries suffer from the slow reaction kinetics and lithium polysulfide (LiPSs) shuttling. To address these issues, a bimetallic sulfide MoS2-SnS heterostructure has been constructed by a salt-template method to modify the separator of Li-S batteries. The 3D porous MoS2-SnS heterostructure on N-doped carbon (MoS2-SnS/NC) can improve the LiPSs adsorption and accelerate the LiPSs conversion and Li2S uniform nucleation/deposition due to its pore structure, polar bond, and built-in electric field at the interface of MoS2 and SnS. Therefore, the prepared MoS2-SnS/NC-PP heterostructure exhibits a high initial capacity (1504.6 mAh g-1), superior rate performance (690.1 mAh g-1 at 4C), and good cycling stability (0.07 % capacity decay rate at 400 cycles at 4C). When the sulfur loading is 3.50 mg cm-2, the Li-S battery delivers a capacity of 635 mAh g-1.
引用
收藏
页数:11
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