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Platinum deposited on TiO2-C and SnO2-C composites for methanol oxidation and oxygen reduction
•The activity of Pt/SnO2-C and Pt/TiO2-C for the MOR was evaluated.•The effect of different oxide on the methanol tolerance was determinate.•Chronoamperometry results confirm the Pt/SnO2-C catalyst stability.•The role of SnO2 can be addressed as co-catalyst of Pt for MOR and ORR. Electrocatalytic ac...
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Published in: | Electrochimica acta 2014-02, Vol.120, p.344-349 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •The activity of Pt/SnO2-C and Pt/TiO2-C for the MOR was evaluated.•The effect of different oxide on the methanol tolerance was determinate.•Chronoamperometry results confirm the Pt/SnO2-C catalyst stability.•The role of SnO2 can be addressed as co-catalyst of Pt for MOR and ORR.
Electrocatalytic activities and stabilities of Pt supported on SnO2-carbon and TiO2-carbon as electrocatalysts were examined for methanol oxidation and oxygen reduction reactions. The Pt/oxide-C catalysts were synthesized by photo-deposition method at RT. The samples prepared were characterized by X-ray diffraction, TEM analysis, cyclic and lineal voltammetry, CO stripping and chronoamperometry techniques. Electrochemical activities of Pt/oxide-C for methanol oxidation reaction (MOR) and methanol tolerance for oxygen reduction were compared with those of Pt/C (Pt-Etek). The MOR activity of Pt/SnO2-C was enhanced over those of the Pt/TiO2-C and Pt/C at different concentrations due to the small platinum particles size. Pt-Sn interaction produce changes in the platinum electronic properties that improve the electrochemical activity towards the methanol oxidation and stability to the methanol presence. The SnO2-C composite appear to be a promising support material that promote electrochemical reactions and stabilize catalytic particles in direct alcohol fuel cells. |
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ISSN: | 0013-4686 1873-3859 |
DOI: | 10.1016/j.electacta.2013.12.055 |