An investigation was carried out in the electro-oxidation of methanol on a carbon-supported quaternary Pt-Ru-Sn-W catalyst prepared by a liquid-phase reduction method. As derived by X-ray diffraction and X-ray photoelectron spectroscopy, the catalyst was composed of metallic Pt, microcrystalline RuO2 and SnO2 phases and amorphous WO3/WO2 species. The electrochemical analysis was carried out in half-cell containing sulfuric acid electrolyte as well as in a liquid methanol-fed solid polymer electrolyte single-cell. The activity of catalyst in the half-cell varied as a function of the methanol concentration, it increased with CH3OH molarity in the activation-controlled region and showed a maximum in 2 M CH3OH at high currents. IR-free polarization curves showed that the activity of the quaternary catalyst was superior to Pt metal/C samples having the same Pt amount. The presence of semi-insulating metal oxides such as RuO2, SnO2 and WO3 on the electrode surface exhibited a significant uncompensated resistance. The single-cell performance was lower than that predicted by the half-cell experiments mainly due to the methanol cross-over through the Nafion membrane.

INVESTIGATION OF A CARBON-SUPPORTED QUATERNARY PT-RU-SN-W CATALYST FOR DIRECT METHANOL FUEL-CELLS

ANTONUCCI V
1995

Abstract

An investigation was carried out in the electro-oxidation of methanol on a carbon-supported quaternary Pt-Ru-Sn-W catalyst prepared by a liquid-phase reduction method. As derived by X-ray diffraction and X-ray photoelectron spectroscopy, the catalyst was composed of metallic Pt, microcrystalline RuO2 and SnO2 phases and amorphous WO3/WO2 species. The electrochemical analysis was carried out in half-cell containing sulfuric acid electrolyte as well as in a liquid methanol-fed solid polymer electrolyte single-cell. The activity of catalyst in the half-cell varied as a function of the methanol concentration, it increased with CH3OH molarity in the activation-controlled region and showed a maximum in 2 M CH3OH at high currents. IR-free polarization curves showed that the activity of the quaternary catalyst was superior to Pt metal/C samples having the same Pt amount. The presence of semi-insulating metal oxides such as RuO2, SnO2 and WO3 on the electrode surface exhibited a significant uncompensated resistance. The single-cell performance was lower than that predicted by the half-cell experiments mainly due to the methanol cross-over through the Nafion membrane.
1995
Istituto di Tecnologie Avanzate per l'Energia - ITAE
METHANOL FUEL CELLS
CATALYSTS
CARBON
PLATINUM
RUTHENIUM
TIN
TUNGSTEN
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/295604
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