Journal
CHEMCATCHEM
Volume 5, Issue 9, Pages 2707-2716Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.201200618
Keywords
gold; oxidation; palladium; nanoparticles; surface analysis
Categories
Funding
- French national project METSA
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A TiO2-supported AuPd bimetallic catalyst with an Au/Pd atomic ratio of 8 was prepared by deposition-precipitation with urea, and its activity in CO oxidation at room temperature was compared to the one of a monometallic Au/TiO2 catalyst. X-ray photoelectron spectroscopy (XPS) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) analyses suggest that Au-Pd/TiO2 contains bimetallic nanoparticles after reduction under H-2 at 500 degrees C although the presence of monometallic Au particles cannot be totally excluded. The evolution of the AuPd nanoparticles surface composition during exposure to O-2 and CO/O-2 was studied insitu by environmental high resolution electron microscopy (ETEM) and DRIFTS. Pd segregation at the surface of the bimetallic nanoparticles was evidenced by DRIFTS and directly observed by ETEM under O-2 and CO/O-2 with the formation of Au-core-Pd-shell structure. The changes in the surface composition of the Au-Pd nanoparticles under CO/O-2 was paralleled with the higher rate of deactivation in the first reaction stages observed for Au-Pd/TiO2 compared to Au/TiO2, which could be related to the possible replacement of Au in low coordination sites, at the origin of the high activity in CO oxidation, by Pd atoms. These results noticeably underline the modifications induced by the reactant that can undergo a bimetallic AuPd catalyst.
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