4.6 Article

Micropore-Dominant Vanadium and Iron Co-Doped MnO2 Hybrid Film Electrodes for High-Performance Supercapacitors

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 163, Issue 13, Pages A2725-A2732

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.0991613jes

Keywords

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Funding

  1. National Natural Science Foundation of China [21103085]
  2. Natural Science Foundation of Jiangxi Province [20151BAB206017]
  3. Education Department Foundation of Jiangxi Province [GJJ150723]
  4. Programme for Key Transfer and Transformation of Scientific Achievements of Jiangxi Province [20151BBI90006]
  5. Foundation for Key Laboratory for Microstructural Control of Metallic Materials of Jiangxi Province [JW201523004]
  6. Programme for Innovation of Science and Technology of Shanxi Province [2015KTZDSF-02-02]
  7. Innovation/Entrepreneurship Programme of Jiangsu Province [suzutong[2013]477, Surencaiban[2015]26]

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To further improve the electrochemical performance of electrode materials for supercapacitors, we have achieved a significant increase of the micropore volume of a MnO2 hybrid film on IrO2 nano-wedges grown on a pre-treated Ti plate by the co-doping of vanadium and iron (V+Fe). X-ray diffraction and microstructural analyses demonstrate that the V+Fe co-doped MnO2 hybrid films consist of the lamellar structure that is composed of gamma-MnO2 nanocrystallites jointed by disordered interface. Nitrogen sorption analysis confirms that the pore characteristics of the MnO2 film change from mesopore-dominant to micropore-dominant after the co-doping, accompanied by increases in the pore volume and specific surface area. The specific capacitance of the V+Fe co-doped MnO2 hybrid film electrode declines from 426 F g(-1) to 314 F g(-1) with a relatively limited loss of 26% when the galvanostatic (GV) charging-discharging rate is increased from 0.2 to 5 A g(-1). In particular, the doped MnO2 film electrode has a loss of only 6% in the specific capacitance after 9000 cycles at a charge-discharge current density of 10 A g(-1). (C) 2016 The Electrochemical Society. All rights reserved.

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