Journal of the Electrochemical Society, Vol.144, No.3, 970-979, 1997
Evaluation of Platinum-Based Catalysts for Methanol Electrooxidation in Phosphoric-Acid Electrolyte
Carbon-supported catalysts of Pt, Pt/Ru, Pt/Ru/W and Pt/Ru/Pd were evaluated for the electro-oxidation of methanol in phosphoric acid at 180 degrees C. These catalysts were characterized using cyclic voltammetry and x-ray diffraction. Addition of Ru to a 0.5 mg/cm(2) Pt catalyst (1:1 atomic ratio) caused a large reduction in polarization. The open-circuit voltage was reduced by 100 mV and polarization at 400 mA/cm(2) was reduced by 180 mV. A Pt/Ru (5:2) catalyst with the same Pt content lowered the open-circuit voltage 70 mV. Additions of W to form Pt/Ru/W (1:1:1, atomic ratio) and Pd to form Pt/Ru/Pd (2:2:1), all with the same platinum loading, gave the same performance as Pt/Ru (1:1) without the additions. All of the catalysts showed two Tafel slopes, 140 mV/dec at lower polarizations and 100 to 120 mV/dec at higher polarizations. indicating that the reaction mechanisms are the same for all of the catalysts. Methanol oxidation is greatly enhanced at 180 degrees C in phosphoric acid compared to the lower operating temperatures of a perfluorosulfonic acid electrolyte. The exchange current density for methanol oxidation is higher than that for O-2 reduction. Ru metal dissolves from catalysts at high potentials. Hydrogen oxidation in the presence of 1 mole percent carbon monoxide showed carbonmonoxide tolerance in the order : Pt/Ru/Pd > Pt/Ru > Pt.
Keywords:SMALL ORGANIC-MOLECULES;AIR FUEL-CELLS;ELECTROCHEMICAL OXIDATION;ANODIC-OXIDATION;SULFURIC-ACID;CARBON;ELECTROOXIDATION;RU;ELECTROCATALYSTS