Issue 5, 2010

The role of the support in COads monolayer electrooxidation on Ptnanoparticles: Pt/WOxvs.Pt/C

Abstract

The electrocatalytic properties of home-made Pt nanoparticles supported onto WOx were determined for the electrooxidation of a COads monolayer and compared with that of a commercial Pt/C having the same Pt particle size. By combining electrochemical and spectroscopic techniques, we found that Pt/WOx nanoparticles exhibit a very high tolerance to CO at low electrode potentials (E = 0.1 V vs. RHE), which was never reported in the literature before. CO adsorption at E = 0.1 V vs. RHE on Pt/WOx yields CO2 production as observed by Fourier-transform infrared spectroscopy (FTIR). When the gas bubbling in solution changes from CO to Ar, the current attenuates and the CO2 production vanishes. This points towards a limited number of “active sites” and a slow step in the electrocatalytic process. When H2 is used to purge the electrolyte from CO, a steep and continuous increase of the H2 electrooxidation current is observed pointing towards continuous liberation of the Pt catalytic sites. The high tolerance to CO of Pt/WOx is discussed in terms of strong metal–support interaction (SMSI), which involves formation of a metal-oxide film partially covering the Pt nanoparticles (encapsulation) and creation of WOH groups upon H+ insertion at low electrode potentials.

Graphical abstract: The role of the support in COads monolayer electrooxidation on Pt nanoparticles: Pt/WOxvs. Pt/C

Article information

Article type
Paper
Submitted
28 Jul 2009
Accepted
12 Nov 2009
First published
10 Dec 2009

Phys. Chem. Chem. Phys., 2010,12, 1182-1193

The role of the support in COads monolayer electrooxidation on Pt nanoparticles: Pt/WOxvs. Pt/C

F. Micoud, F. Maillard, A. Bonnefont, N. Job and M. Chatenet, Phys. Chem. Chem. Phys., 2010, 12, 1182 DOI: 10.1039/B915244J

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