Probing the metal sites of a vanadium oxide-Pd(111) 'inverse catalyst': adsorption of CO

Citation
Fp. Leisenberger et al., Probing the metal sites of a vanadium oxide-Pd(111) 'inverse catalyst': adsorption of CO, SURF SCI, 444(1-3), 2000, pp. 211-220
Citations number
33
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
SURFACE SCIENCE
ISSN journal
00396028 → ACNP
Volume
444
Issue
1-3
Year of publication
2000
Pages
211 - 220
Database
ISI
SICI code
0039-6028(20000101)444:1-3<211:PTMSOA>2.0.ZU;2-6
Abstract
The adsorption of CO on V-oxide covered Pd(111) multicomponent surfaces, so -called 'inverse catalyst' surfaces, has been studied by high-resolution X- ray photoelectron spectroscopy using synchrotron radiation. Since CO does n ot chemisorb on V oxide surfaces at room temperature, the adsorption of CO reflects the reactivity of the free Pd sites of this inverse catalyst surfa ce. The C 1s and Pd 3d core level spectra have been monitored to follow the CO surface coverage as a function of CO exposure and V oxide coverage and to investigate the CO adsorption sires. The results indicate that the adsor ption of CO on V-oxide/Pd(111) surfaces is kinetically influenced by the V oxide phase via spill-over of CO molecules from a mobile physisorbed precur sor state on the oxide surface on to Pd sites. As a result of this spill-ov er effect the initial sticking probability of CO per free Pd site increases beyond unity with increasing oxide coverage. The analysis of C 1s binding energies as a function of CO and oxide coverage suggests that the distribut ion of CO adsorption sites is altered by the V-oxide/Pd phase boundary. (C) 2000 Elsevier Science B.V. All rights reserved.