Nanoporous Platinum Electrodes as Substrates for Metal Oxide-Supported Noble Metal Electrocatalytic Nanoparticles: Synergistic Effects During Electrooxidation of Ethanol

被引:7
|
作者
Rutkowska, Iwona A. [1 ]
Koster, Margaretta D. [2 ]
Blanchard, Gary J. [2 ]
Kulesza, Pawel J. [1 ]
机构
[1] Univ Warsaw, Dept Chem, PL-02093 Warsaw, Poland
[2] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
关键词
IN-SITU FTIR; ELECTROCHEMICAL OXIDATION; PT/RU NANOPARTICLES; METHANOL OXIDATION; FUEL-CELLS; OPAL FILMS; CATALYSTS; DEMS; PERMSELECTIVITY; ENHANCEMENT;
D O I
10.1071/CH14264
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrocatalytic oxidation of ethanol in acid medium (0.5moldm(-3) H2SO4) was significantly enhanced by not only supporting bimetallic PtRu nanoparticles on nanostructured metal oxides (TiO2 or WO3), but also by depositing such catalytic systems on planar nanoporous platinized electrode substrates. Incorporation of TiO2 or WO3 into the electrocatalytic interface was likely to improve proton mobility and to provide -OH groups capable of inducing the removal of poisoning species, such as CO, from the Pt sites in the bimetallic PtRu catalyst. Synergistic interactions between ruthenium and titania were also possible. Regularly porous nanostructured platinum substrate also permitted development of submicro reactors' where reactant molecules, electrolyte ions, and all active components (TiO2 or WO3, Pt substrate, PtRu catalytic sites) could co-exist and become easily accessible. While WO3 was able to undergo fast reversible redox transitions to non-stoichiometric oxides, efficient utilization of inert (non-electroactive) TiO2 required admixing with carbon nanotubes to ensure easy charge distribution and good conductivity at the electrocatalytic interface.
引用
收藏
页码:1414 / 1421
页数:8
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