Effect of Fe3+ on the synthesis and electrochemical performance of nanostructured MnO2

被引:13
|
作者
Wang, Jian-Gan [1 ,3 ]
Yang, Ying [2 ]
Huang, Zheng-Hong [1 ]
Kang, Feiyu [1 ,3 ]
机构
[1] Tsinghua Univ, State Key Lab New Ceram & Fine Proc, Dept Mat Sci & Engn, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Dept Elect Engn, Beijing 100084, Peoples R China
[3] Tsinghua Univ, Inst Adv Mat Res, Grad Sch Shenzhen, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
Nanostructures; Chemical synthesis; Crystal structure; Electrochemical properties; SHAPE-CONTROLLED SYNTHESIS; HYDROTHERMAL SYNTHESIS; PSEUDOCAPACITANCE PROPERTIES; ALPHA-MNO2; OXIDE; ELECTRODES; NANORODS; CARBON;
D O I
10.1016/j.matchemphys.2012.01.056
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Different MnO2 nanostructures were synthesized in stoichiometric KMnO4/MnSO4 aqueous solutions in the absence/presence of Fe3+ at temperature ranging from 30 degrees C to 180 degrees C. The phase structures, morphologies and electrochemical properties of the as-prepared MnO2 products were investigated using X-ray powder diffraction, scanning electron microscope, N-2 physical adsorption and cyclic voltammetry techniques. The results showed that the presence of Fe3+ addition had a significant effect on the phase structural evolution, morphological features and electrochemical properties of the MnO2 products. Fe3+ was found to greatly prevent the epitaxial growth and crystallization of MnO2 nucleus, which in turn influenced textual characteristics. The electrochemical performance of the nanostructured MnO2 products had a complex relationship with the phase structures, specific surface area as well as pore characteristics. MnO2 prepared in the presence of Fe3+ (KMF-MnO2) showed relatively higher specific capacitance compared to that of MnO2 prepared in the absence of Fe3+ (KM-MnO2). Maximum capacitance of 214 Fg(-1) was obtained for KMF-MnO2 prepared at 30 degrees C at a scan rate of 2 mV s(-1) in 0.1 M Na2SO4 electrolyte. (C) 2012 Elsevier By. All rights reserved.
引用
收藏
页码:437 / 444
页数:8
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