New Strategy for the Morphology-Controlled Synthesis of V2O5 Microcrystals with Enhanced Capacitance as Battery-type Supercapacitor Electrodes

被引:109
作者
Zheng, Jiqi [1 ]
Zhang, Yifu [1 ]
Hu, Tao [1 ]
Lv, Tianming [1 ]
Meng, Changgong [1 ]
机构
[1] Dalian Univ Technol, Sch Chem, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
HIGH-PERFORMANCE CATHODE; REDUCED GRAPHENE OXIDE; VANADIUM PENTOXIDE; HYDROTHERMAL SYNTHESIS; HYBRID SUPERCAPACITOR; TEMPLATE; NANOWIRES; SPHERES; ARRAYS; HETEROSTRUCTURES;
D O I
10.1021/acs.cgd.8b00776
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Porous vanadium pentoxide (V2O5) microcrystals with different morphologies were synthesized through the decomposition of butterfly-like, rhombohedral, and flower-like ammonium metavanadate (NH4VO3) microcrystals, which were synthesized by the drowning-out crystallization of hydrothermal NH4VO3 aqueous solution using ethanol as both the antisolvent and the template for the self-assembly of vanadate ions. The effects of reaction conditions on the morphologies of products were characterized by scanning electron microscopy (SEM), and the possible growth mechanism was proposed. The electrochemical properties of the produced porous V2O5 with different morphologies were studied as battery-type electrodes for supercapacitors using 1 M LiClO4/propylene carbonate (PC) as the electrolyte. Rhombohedral V2O5 exhibited the highest initial specific capacitance of 641 F.g(-1) at 0.5 A.g(-1) among the three obtained morphologies, as well as an excellent rate capability and cycling stability, with a retention of over 119% after 2000 cycles, making it a promising electrode material for supercapacitors. The influences of morphologies on the capacitance and cycle performance are analyzed. The results indicate that the increasing complexity of the structure leads to lower specific capacitance because of the higher degree of electrode polarization and higher resistance, while the structure stability of the microcrystals is related to the rate capability as well as the cycling performance.
引用
收藏
页码:5365 / 5376
页数:12
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