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Electrochemical impedance studies on carbon supported PtRuNi and PtRu anode catalysts in acid medium for direct methanol fuel cell

  • Zhen Bo Wang*
  • , Ge Ping Yin
  • , Yu Yan Shao
  • , Bo Qian Yang
  • , Peng Fei Shi
  • , Peter Xian Feng
  • *Corresponding author for this work
  • Harbin Institute of Technology
  • University of Puerto Rico

Research output: Contribution to journalArticlepeer-review

Abstract

The anodic Pt-Ru-Ni/C and the Pt-Ru/C catalysts for potential application in direct methanol fuel cell (DMFC) were prepared by chemical reduction method. Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) measurements were carried out by using a glassy carbon working electrode covered with the catalyst powder in a solution of 0.5 mol L-1 CH3OH and 0.5 mol L-1 H2SO4 at 25 °C. EIS information discloses that the methanol electrooxidation on the Pt-Ru-Ni/C catalyst at various potentials shows different impedance behaviors. The mechanism and the rate-determining step of methanol electrooxidation are changed with increasing potential. Its rate-determining steps are the methanol dehydrogenation and the oxidation reaction of adsorbed intermediate COads and OHads in low (400-500 mV) and high (600-800 mV) potentials, respectively. The catalytic activity of the Pt-Ru-Ni/C catalyst is higher for methanol electrooxidation than that of the Pt-Ru/C catalyst. Its tolerance performance to CO formed as one of the intermediates of methanol dehydrogenation is also better than that of the Pt-Ru/C catalyst.

Original languageEnglish
Pages (from-to)9-15
Number of pages7
JournalJournal of Power Sources
Volume165
Issue number1
DOIs
StatePublished - 25 Feb 2007

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

Keywords

  • Direct methanol fuel cell
  • Electrochemical impedance
  • Methanol electrooxidation
  • Pt-Ru-Ni/C catalyst
  • Pt-Ru/C catalyst

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