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 language | English |
|---|---|
| Pages (from-to) | 9-15 |
| Number of pages | 7 |
| Journal | Journal of Power Sources |
| Volume | 165 |
| Issue number | 1 |
| DOIs | |
| State | Published - 25 Feb 2007 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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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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