Vertically aligned VS2 on graphene as a 3D heteroarchitectured anode material with capacitance-dominated lithium storage

被引:76
作者
Huang, Zhiyong [1 ,2 ]
Han, Xiaoyan [1 ,2 ]
Cui, Xun [3 ,4 ,5 ]
He, Chengen [1 ,2 ,4 ,5 ]
Zhang, Jinlong [4 ,5 ]
Wang, Xianggang [4 ,5 ]
Lin, Zhiqun [3 ]
Yang, Yingkui [1 ,2 ,4 ,5 ]
机构
[1] South Cent Univ Nationalities, Key Lab Catalysis & Energy Mat Chem, Minist Educ, Wuhan 430074, Peoples R China
[2] South Cent Univ Nationalities, Sch Chem & Mat Sci, Hubei Key Lab Catalysis & Mat Sci, Wuhan 430074, Peoples R China
[3] Georgia Inst Technol, Sch Mat Sci & Engn, Atlanta, GA 30332 USA
[4] Guangdong Xigu Tanyuan New Mat Corp Ltd, Graphene R&D Ctr, Foshan 528000, Peoples R China
[5] South Cent Univ Nationalities, Foshan 528000, Peoples R China
基金
中国国家自然科学基金;
关键词
ENERGY-CONVERSION; 2-DIMENSIONAL NANOMATERIALS; ELECTROCHEMICAL PROPERTIES; HIERARCHICAL ARCHITECTURE; HYDROTHERMAL SYNTHESIS; RATE CAPABILITY; WS2; NANOSHEETS; ION BATTERIES; COMPOSITE; PERFORMANCE;
D O I
10.1039/c9ta13835h
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
Vertically aligned 2D few-layered VS2 nanosheets onto a 2D graphene substrate were, for the first time, crafted by scalable solvothermal and post-annealing processes. The resulting 3D heterostructured VS2-on-graphene (denoted as VS2@Gr) is composed of interconnected nanosheet networks with an efficient exposure of electrochemically active surfaces, nanosheet edges, and abundant porous channels. Such robust hierarchical architectures possess significant advantages over individual building blocks, inhibiting intersheet aggregation, facilitating electrolyte percolation/active-material utilization, promoting ion diffusion/electron conduction, and retaining structural integrity/mechanical stability. Surprisingly, these synergetic characteristics endow VS2@Gr with very favorable capacitive kinetics in the Li-storage behavior. When employed as an anode, the VS2@Gr exhibits remarkable electrochemical performance with large reversible capacity (989 mA h g(-1) at 0.1 A g(-1)), high initial coulombic efficiency (64%), a larger ion diffusion coefficient, superior rate capability (675 mA h g(-1) at 1 A g(-1)), and long cycling stability (77% retention at 10 A g(-1) after 10 000 cycles), outperforming its VS2 counterpart with a dominant diffusion-controlled behavior. This work may provide new insights into the architectural engineering of 3D heterostructured nanomaterials comprising two dissimilar 2D constituents for advanced energy storage.
引用
收藏
页码:5882 / 5889
页数:8
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