Tin oxide (SnO2) nanoparticles/electrospun carbon nanofibers (CNFs) heterostructures: Controlled fabrication and high capacitive behavior

被引:85
作者
Mu, Jingbo [1 ]
Chen, Bin [1 ]
Guo, Zengcai [1 ]
Zhang, Mingyi [1 ]
Zhang, Zhenyi [1 ]
Shao, Changlu [1 ]
Liu, Yichun [1 ]
机构
[1] NE Normal Univ, Dept Chem, Changchun 130024, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrospinning; Carbon nanofibers; Tin oxide; Heterostructures; Electrochemical performance; THIN-FILMS; HYDROTHERMAL SYNTHESIS; SONOCHEMICAL SYNTHESIS; COMPOSITE ELECTRODES; PERFORMANCE; SURFACE; MNO2;
D O I
10.1016/j.jcis.2011.01.032
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
Tin oxide (SnO2)/carbon nanofibers (CNFs) heterostructures were fabricated by combining the versatility of the electrospinning technique and template-free solvent-thermal process. The results revealed that the SnO2 nanostructures were successfully grown on the primary electrospun carbon nanofibers substrates. And, the coverage density of SnO2 nanoparticles coating on the surface of the CNFs could be controlled by simply adjusting the mass ratio of CNFs to SnCl4 center dot 5H(2)O in the precursor during the solventthermal process for the fabrication of SnO2/CNFs heterostructures. The electrochemical performances of the SnO2/CNFs heterostructures as the electrode materials for supercapacitors were evaluated by cyclic voltammetry (CV) and galvanostatic charge-discharge measurement in 1M H2SO4 solution. At different scan rates, all the samples with different coverage densities of SnO2 showed excellent capacitance behavior. And, the sample CS2 (the mass ratio of CNFs to SnCl4 center dot 5H(2)O reached 1:7) exhibited a maximum specific capacitance of 187 F/g at a scan rate of 20 mV/s. Moreover, after 1000 cycles, the specific capacitance retention of this sample was over 95%. The high capacitive behavior could be ascribed to the low resistance of SnO2/CNFs heterostructures and rapid transport of the electrolyte ions from bulk solution to the surface of SnO2. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:706 / 712
页数:7
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