Electrocatalytic Activity and Stability of Titania-Supported Platinum–Palladium Electrocatalysts for Polymer Electrolyte Membrane Fuel Cell

Titania-supported platinum–palladium electrocatalysts (PtPd/TiO2) were synthesized and investigated as alternative catalysts for the oxygen reduction reaction (ORR). Transmission electron microscope images revealed a uniform distribution of metal nanoparticles (d M = 3–5 nm) on the TiO2 support. An...

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Veröffentlicht in:ACS catalysis 2012-05, Vol.2 (5), p.825-831
Hauptverfasser: Huang, Sheng-Yang, Ganesan, Prabhu, Popov, Branko N
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Popov, Branko N
description Titania-supported platinum–palladium electrocatalysts (PtPd/TiO2) were synthesized and investigated as alternative catalysts for the oxygen reduction reaction (ORR). Transmission electron microscope images revealed a uniform distribution of metal nanoparticles (d M = 3–5 nm) on the TiO2 support. An increase in ORR activity has been observed with an increase in the Pd content of the bimetallic alloy up to 30%, and beyond this composition, the decrease in catalytic activity has been found to be due to the blocking of Pt active sites by a large amount of Pd in the catalyst. The PtPd/TiO2 electrocatalyst with a Pt/Pd composition of 70:30 shows activity comparable to that of a commercial Pt/C catalyst (TKK) in rotating ring-disk electrode studies. The accelerated durability test results show good stability for the PtPd/TiO2 electrocatalysts at high potentials in terms of minimum loss in the Pt electrochemical surface area. The high stability of the PtPd/TiO2 electrocatalyst synthesized in this investigation offers a new approach to improve the reliability and durability of polymer electrolyte membrane-based fuel cell cathode catalysts.
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Transmission electron microscope images revealed a uniform distribution of metal nanoparticles (d M = 3–5 nm) on the TiO2 support. An increase in ORR activity has been observed with an increase in the Pd content of the bimetallic alloy up to 30%, and beyond this composition, the decrease in catalytic activity has been found to be due to the blocking of Pt active sites by a large amount of Pd in the catalyst. The PtPd/TiO2 electrocatalyst with a Pt/Pd composition of 70:30 shows activity comparable to that of a commercial Pt/C catalyst (TKK) in rotating ring-disk electrode studies. The accelerated durability test results show good stability for the PtPd/TiO2 electrocatalysts at high potentials in terms of minimum loss in the Pt electrochemical surface area. 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