4.4 Article

Au/C catalyst prepared by polyvinyl alcohol protection method for direct alcohol alkaline exchange membrane fuel cell application

Journal

JOURNAL OF APPLIED ELECTROCHEMISTRY
Volume 42, Issue 7, Pages 483-490

Publisher

SPRINGER
DOI: 10.1007/s10800-012-0423-3

Keywords

Au/C; PVA protection method; Alcohol electrooxidation; Ethanol; Ethylene glycol; Glycerol

Funding

  1. National Nanotechnology Center of Thailand (NANOTEC)
  2. Joint Graduate School of Energy and Environment (JGSEE)
  3. Thailand Research Fund (TRF)

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An Au/C catalyst was prepared by means of the polyvinyl alcohol-protected Au sol method. Highly dispersed Au nanoparticles with an average particle size of around 3.7 nm were obtained as confirmed by transmission electron microscopy. The cyclic voltammogram of Au/C was similar to that of a bulk Au electrode, but a small shift of Au oxide reduction and oxidation potential peaks were observed. The electrooxidation of methanol, ethanol, ethylene glycol, and glycerol on the Au/C catalyst in an alkaline solution was analyzed. Using a cyclic voltammogram, the maximum current density toward alcohol electrooxidation was found to decrease in the order of glycerol > ethylene glycol > ethanol, while methanol was not oxidized. Compared with PtRu/C, the maximum current densities obtained from the Au/C catalyst for ethylene glycol and glycerol electrooxidation were increased by 1.6 and 3.3 times, respectively. The reaction heavily progressed through a C-C bond dissociation path. It was found that main product of glycerol electrooxidation was formic acid, which accounted for more than 60 % of the total product. Using chronoamperometry, the Au/C catalyst showed much better stability than that of PtRu/C for the reaction without C-C bond dissociation and better stability for the reaction with C-C bond dissociation.

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