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Preparation and characterization of Ti0.7Sn0.3O2 as catalyst support for oxygen reduction reaction
Sn-doped TiO2 nanoparticles with high surface area of 125.7 m2·g-1 are synthesized via a simple one-step hydrothermai method and explored as the cathode catalyst support for proton exchange membrane fuel cells.The synthesized support materials are studied by X-ray diffraction analysis,energy dispers...
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Published in: | Journal of energy chemistry 2014-05, Vol.23 (3), p.331-337 |
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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: | Sn-doped TiO2 nanoparticles with high surface area of 125.7 m2·g-1 are synthesized via a simple one-step hydrothermai method and explored as the cathode catalyst support for proton exchange membrane fuel cells.The synthesized support materials are studied by X-ray diffraction analysis,energy dispersive X-ray spectroscopy and transmission electron microscopy.It is found that the conductivity has been greatly improved by the addition of 30 mol%Sn and Pt nanoparticles are well dispersed on Ti0.7Sn0.3O2 support with an average size of 2.44 run.Electrochemical studies show that the Ti0.7Sn0.3O2 nanoparticles have excellent electrochemical stability under a high potential compared to Vulcan XC-72.The as-synthesized Pt/Ti0.7Sn0.3O2 exhibits high and stable electrocatalytic activity for the oxygen reduction reaction.The Pt/Ti0.7Sn0.3O2 catalyst reserves most of its electrochemically active surface area(ECA),and its half wave potential difference is 11 mV,which is lower than that of Pt/XC-72(36 mV) under 10 h potential hold at 1.4 V vs.NHE.In addition,the ECA degradation of Pt/Ti0.7Sn0.3O2is 1.9 times lower than commercial Pt/XC-72 under 500 potential cycles between 0.6 V and 1.2 V vs.NHE.Therefore,the as synthesized Pt/Ti0.7Sn0.3O2 can be considered as a promising alternative cathode,catalyst for proton exchange membrane fuel cells. |
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ISSN: | 2095-4956 |
DOI: | 10.1016/S2095-4956(14)60155-8 |