Fabrication of mesoporous carbon hollow spheres intercalated three-dimensional network structure V2O5 nanosheets with enhanced electrochemical performance

被引:16
作者
Zhang, Gaini [1 ]
Ren, Lijun [1 ]
Hu, Dengwei [1 ]
Zhang, Sheng [1 ]
Gu, Hongxi [1 ]
机构
[1] Baoji Univ Arts & Sci, Coll Chem & Chem Engn, Engn Res Ctr Adv Ferroelect Funct Mat, Key Lab Phytochem Shaanxi Prov, Baoji 721013, Peoples R China
基金
中国国家自然科学基金;
关键词
Mesoporous carbon hollow spheres; Vanadium pentoxide; Hybrid materials; Hierarchical porous structure; Electrochemical property; REDUCED GRAPHENE OXIDE; VANADIUM-OXIDE; COMPOSITE ELECTRODES; ANODE MATERIAL; SUPERCAPACITOR; HYBRID; NANOCOMPOSITE; POLYPYRROLE; NANOWIRES; AEROGELS;
D O I
10.1016/j.jallcom.2018.12.096
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
Two-dimensional vanadium pentoxide (V2O5) nanosheets has attracted attention for electrochemical energy storage because of the presence of redox active and unique layered structures available for ions diffusion. However, current strategies are largely limited to enhancing the electrochemical kinetics of V2O5. Combining three-dimensional (3D) V2O5 network with mesoporous carbon hollow spheres (MCHS) is an effective method to improve the electric transport properties of V2O5 because such combinations not only prevent the restacking of V2O5 nanosheets, but also enhance electronic transport. The obtained structure possessed 3D V2O5 nanosheets interconnected with MCHS, producing a 3D hierarchical porous structure MCHS/V2O5 hybrid materials. The continuous 3D porous network not only creates channels for better ions diffusion, electron transport and efficient utilization of active V2O5 and MCHS, but also reduces the internal resistance of electrodes, which leads to superior electrochemical performance of 313 F g(-1) at a current density of 0.25 A g(-1), remarkable rate performance with 86.9% capacitance retention in the range of 0.25-10 A g(-1) and cycling performance of 81% over 4000 cycles. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:407 / 414
页数:8
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