Hydrogen interaction with a ceria-zirconia supported gold catalyst. Influence of CO co-adsorption and pre-treatment conditions

S.E. COLLINS, J.M. CÍES, E. DEL RÍO, J.M. PINTADO, S. TRASOBARES, J.J. CALVINO, S. BERNAL

The Journal of Physical Chemistry C

American Chemical Society

Año: 2007 vol. 111 p. 14371 - 14379

1932-7447

This work reports on the hydrogen interaction with a 3 wt % Au/Ce0.62Zr0.38O2 (Au/CZ) catalyst prepared by deposition-precipitation. As deduced from X-ray powder diffraction, electron microscopy (scanning transmission electron  icroscopy-high-angle angular dark field and high-resolution electron microscopy),and CO volumetric/Fourier transform IR (FTIR) adsorption studies, the investigated catalyst shows a good metal dispersion. By combining FTIR spectroscopy and volumetric chemisorption studies, it is shown that upon treating the Au/CZ catalyst with 40 Torr of H2 at room temperature a fast and very intense spillover effect  occurs. As determined from the recorded isotherm, very high values of the apparent H/Au ratio (>8.0) and of the atomic hydrogen surface density (>11.0 H/nm2) are reached. In parallel with this observation, the onset of a characteristic IR band at 2133 cm-1 shows the occurrence of significant support reduction with inherent appearance of Ce3+ species. Moreover, the simultaneous growth of the IR band at 1630 cm-1 due to molecular water strongly suggests that even at room temperature oxygen vacancies are also formed. Additional FTIR spectroscopy studies have shown that the hydrogen spillover is strongly inhibited by either co-adsorption of CO or a reducing pretreatment with flowing 5% H2/Ar at 673 K. These deactivation effects, however, may be reverted by very mild regeneration treatments at room temperature.