Vanadium Intercalation into Niobium Disulfide to Enhance the Catalytic Activity for Lithium-Sulfur Batteries

被引:36
作者
Cheng, Huiting [1 ,2 ]
Shen, Zihan [2 ]
Liu, Wan [1 ]
Luo, Mingting [2 ]
Huo, Fengwei [3 ]
Hui, Junfeng [1 ]
Zhu, Qingshan [2 ,4 ]
Zhang, Huigang [1 ,2 ,4 ]
机构
[1] Northwest Univ, Shaanxi R&D Ctr Biomat & Fermentat Engn, Sch Chem & Engn, Shaanxi Key Lab Degradable Biomed Mat, Xian 710069, Shaanxi, Peoples R China
[2] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
[3] Nanjing Tech Univ, Inst Adv Mat IAM, Key Lab Flexible Elect KLOFE, Nanjing 211816, Peoples R China
[4] Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
lithium-sulfurbatteries; catalysis; shuttle effect; adsorption; niobium disulfide; vanadium disulfide; HYDROGEN EVOLUTION; POLYSULFIDE;
D O I
10.1021/acsnano.3c02634
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despitetheir high specific energy and great promisefor next-generationenergy storage, lithium-sulfur (Li-S) batteries sufferfrom polysulfide shuttling, slow redox kinetics, and poor cyclability.Catalysts are needed to accelerate polysulfide conversion and suppressthe shuttling effect. However, a lack of structure-activityrelationships hinders the rational development of efficient catalysts.Herein, we studied the Nb-V-S system and proposed aV-intercalated NbS2 (Nb3VS6) catalystfor high-efficiency Li-S batteries. Structural analysis andmodeling revealed that undercoordinated sulfur anions of [VS6] octahedra on the surface of Nb3VS6 may breakthe catalytic inertness of the basal planes, which are usually theprimary exposed surfaces of many 2D layered disulfides. Using Nb3VS6 as the catalyst, the resultant Li-Sbatteries delivered high capacities of 1541 mAh g(-1) at 0.1 C and 1037 mAh g(-1) at 2 C and could retain73.2% of the initial capacity after 1000 cycles. Such an intercalation-inducedhigh activity offers an alternative approach to building better Li-Scatalysts.
引用
收藏
页码:14695 / 14705
页数:11
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