4.7 Article

High activity of Au-Cu/C electrocatalyst as anodic catalyst for direct borohydride-hydrogen peroxide fuel cell

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 36, Issue 24, Pages 15775-15782

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2011.09.019

Keywords

Direct borohydride-hydrogen peroxide fuel cell; Au-Cu/C; Bimetallic nanoparticles; Borohydride oxidation; Anode electrocatalyst

Funding

  1. National Natural Science Foundation of China [20871101, 51072173]
  2. Ministry of Education of China [20094301110005]
  3. Science and Technology Plan Project of Hunan Province [2010GK3181]
  4. Hunan Provincial Education Department [11C1207]

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Carbon supported Au-Cu bimetallic nanoparticles are prepared by a modified NaBH4 reduction method in aqueous solution at room temperature. The electrocatalytic activities of the Au-Cu/C catalysts are investigated by cyclic voltammetry, chronoamperometry, chronopotentiometry and fuel cell experiments. It has been found that the Au-Cu/C catalysts have much higher catalytic activity for the direct oxidation of BH4- than Au/C catalyst. Especially, the Au67Cu33/C catalyst presents the highest catalytic activity for BH4- electrooxidation among all as-prepared catalysts, and the DBHFC using Au67Cu33/C anode catalyst and Au/C cathode catalyst shows the maximum power density of 51.8 mW cm(-2) at 69.5 mA cm(-2) and 20 degrees C. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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