Co-Construction of Sulfur Vacancies and Heterojunctions in Tungsten Disulfide to Induce Fast Electronic/Ionic Diffusion Kinetics for Sodium-Ion Batteries

被引:334
|
作者
Li, Yu [1 ,3 ]
Qian, Ji [1 ]
Zhang, Minghao [1 ]
Wang, Shuo [2 ]
Wang, Zhaohua [1 ]
Li, Maosheng [3 ]
Bai, Ying [1 ]
An, Qinyou [3 ]
Xu, Huajie [4 ]
Wu, Feng [1 ,5 ]
Mai, Liqiang [3 ]
Wu, Chuan [1 ,5 ]
机构
[1] Beijing Inst Technol, Sch Mat Sci & Engn, Beijing Key Lab Environm Sci & Engn, Beijing 100081, Peoples R China
[2] Peking Univ, Coll Engn, Dept Mat Sci & Engn, Beijing 100871, Peoples R China
[3] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[4] Zhengzhou Univ, Minist Educ, Key Lab Mat Proc & Mold, Zhengzhou 450002, Peoples R China
[5] Collaborat Innovat Ctr Elect Vehicles Beijing, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
anodes; bimetallic sulfides; heterojunctions; sodium-ion batteries; sulfur vacancies; IN ELECTRIC-FIELD; STORAGE PROPERTIES; CHARGE-TRANSFER; WS2; NANOSHEETS; ANODE MATERIAL; LITHIUM-ION; PERFORMANCE; CARBON; NANOWIRES; HETEROSTRUCTURES;
D O I
10.1002/adma.202005802
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Engineering novel electrode materials with unique architectures has a significant impact on tuning the structural/electrochemical properties for boosting the performance of secondary battery systems. Herein, starting from well-organized WS(2)nanorods, an ingenious design of a one-step method is proposed to prepare a bimetallic sulfide composite with a coaxial carbon coating layer, simply enabled by ZIF-8 introduction. Rich sulfur vacancies and WS2/ZnS heterojunctions can be simultaneously developed, that significantly improve ionic and electronic diffusion kinetics. In addition, a homogeneous carbon protective layer around the surface of the composite guarantees an outstanding structural stability, a reversible capacity of 170.8 mAh g(-1)after 5000 cycles at a high rate of 5 A g(-1). A great potential in practical application is also exhibited, where a full cell based on the WS2-x/ZnS@C anode and the P2-Na(2/3)Ni(1/3)Mn(1/3)O(2)cathode can maintain a reversible capacity of 89.4 mAh g(-1)after 500 cycles at 1 A g(-1). Moreover, the underlying electrochemical Na storage mechanisms are illustrated in detail by theoretical calculations, electrochemical kinetic analysis, and operando X-ray diffraction characterization.
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页数:9
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