Study of mixed ternary transition metal ferrites as potential electrodes for supercapacitor applications

被引:210
作者
Bhujun, Bhamini [1 ]
Tan, Michelle T. T. [1 ,2 ]
Shanmugam, Anandan S. [1 ]
机构
[1] Univ Nottingham, Fac Engn, Dept Elect & Elect Engn, Malaysia Campus, Semenyih 43500, Selangor, Malaysia
[2] Univ Nottingham, Fac Engn, Ctr Nanotechnol & Adv Mat, Malaysia Campus, Semenyih 43500, Selangor, Malaysia
关键词
Mixed ternary transition metal ferrite (MTTMF); Nanocomposites; Sol-gel; Cyclic voltammetry; Asymmetric supercapacitor; AUTO-COMBUSTION; CHEMICAL-SYNTHESIS; NICKEL; PERFORMANCE; GRAPHENE; COMPOSITE; OXIDE; BEHAVIOR; FILM; TEMPERATURE;
D O I
10.1016/j.rinp.2016.04.010
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
Nanocrystallites of three mixed ternary transition metal ferrite (MTTMF) were prepared by a facile solgel method and adopted as electrode material for supercapacitors. The phase development of the samples was determined using Fourier transform infrared (FT-IR) and thermal gravimetric analysis (TG). X-ray diffraction (XRD) analysis revealed the formation of a single-phase spinel ferrite in CuCoFe2O4 (CuCoF), NiCoFe2O4 (NiCoF) and NiCuFe2O4 (NiCuF). The surface characteristics and elemental composition of the nanocomposites have been studied by means of field emission scanning electron microscopy (FESEM), as well as energy dispersive spectroscopy (EDS). The electrochemical performance of the nanomaterials was evaluated using a two-electrode configuration by cyclic voltammetry, electrochemical impedance spectroscopy and galvanostatic technique in 1 M KOH electrolyte and was found to be in the order of: CuCoF > NiCoF > NiCuF. A maximum specific capacitance of 221 Fg(-1) was obtained with CuCoF at a scan rate of 5 mV s(-1). In addition to an excellent cycling stability, an energy density of 7.9 kW kg(-1) was obtained at a current density of 1 Ag-1. The high electrochemical performance of the MTTMF nanocomposites obtained indicates that these materials are promising electrodes for supercapacitors. (C) 2016 The Authors. Published by Elsevier B. V. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:345 / 353
页数:9
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