4.7 Article

Electrocatalytic performance of Ni modified MnOX/C composites toward oxygen reduction reaction and their application in Zn-air battery

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 39, 期 7, 页码 3423-3432

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2013.12.076

关键词

Oxygen reduction reaction; Manganese oxide; Nickel hydroxide; Activity; Zinc-air battery

资金

  1. National Basic Research Program of China [2012CB215500]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA09030104]
  3. Natural Science Foundation of China [21106142]
  4. Hi-Tech R&D Program of China [2011AA050705]
  5. External Cooperation Program of the Chinese Academy of Sciences [GJHZ1135]

向作者/读者索取更多资源

A series of Ni modified MnOx/C composites were synthesized by introducing NaBH4 to MnO2/C aqueous suspension containing Ni(NO3)(2). The physical properties and the activity of the composites toward the oxygen reduction reaction (ORR) were investigated via transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and the electrochemical techniques. The results show that the higher activity of the composites toward the ORR is correlated with the higher content of Mn0OH species transformed from Mn(II) on the surface of the composite. The main nickel species in the composites is Ni(OH)(2), while Ni(OH)(2) shows little activity toward the ORR. However, introducing Ni(OH)2 with proper amount into the MnOx/C improves the distribution of the active material MnOx, which contributes to a surface with more MnOOH. The optimal composite is of the Ni/Mn atomic ratio of 1:2 and the MnOx loading of 28 wt.%. The maximum power density of the zinc-air battery with the optimized Ni modified MnOx/C as the cathode catalyst reaches up to 122 mW cm(-2), much higher than the one with the MnOx/ C as the air cathode catalyst (89 mW cm(-2)), and slightly higher than those with the Pd/C and Pt/C as the cathode catalysts. Crown Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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