The Journal of Physical Chemistry B · 2004 · 39 citations · 45 references
Natural SciencesChemistryMaterials SciencePhysical ChemistrySurface ChemistrySurface ScienceMetal OxidesSurface AdsorptionSurface KineticsSurface OxidationSurface PhysicsSurface ReactionsAdsorption On Oxide SurfacesAdsorption On OxidesNitric OxidePretreatmentSurface Chemistry Of OxidationSurface CoverageSurface Coverage AnalysisSurface Temperature
The effect of the pretreatment on the interaction between NO and Au−TiO 2 was examined using DRIFTS as a monitoring tool. For calcined and reduced Au−TiO 2, adsorption of NO on the TiO 2 support is not promoted under the conditions employed. Au(NO) 2 is the predominant species on oxidized and reduced Au−TiO 2 with initial bands at 1818 and 1740 cm -1 . Analysis showed that these species are sensitive to the surface coverage, temperature, and the state of the underlying surface, shifting from 1820 cm -1 for reduced Au−TiO 2 to 1850 cm -1 for oxidized Au−TiO 2 and from 1740 to 1734 cm -1 with increasing surface temperature. It is proposed that different dinitrosyl components are formed on the surface and are bonded to Au sites in different chemical environments. Small dissociative contributions (N 2 O formation) were detected at higher NO pressures and temperatures. Adsorption of NO on oxidized Au−TiO 2 is dominated by bridging NO adsorbates (bands at 1665 and 1641 cm -1 ) at low NO exposures, but linearly bound NO (bands at 1873, 1860, 1838, and 1808 cm -1 ) were detected with increasing NO coverage. Products of dissociation and associated mainly with the TiO 2 support dominate the spectra for oxidized Au−TiO 2 .
45