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A High Pressure PM-IRRAS Study of CO and O2 Coadsorption and Reactivity on PtSn Alloy Surfaces

Authors :
Francisco José Cadete Santos Aires
David Loffreda
Eric Ehret
Y. Jugnet
Françoise Delbecq
Céline Dupont
Institut de recherches sur la catalyse et l'environnement de Lyon (IRCELYON)
Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)
Laboratoire de Chimie - UMR5182 (LC)
Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL)
Université de Lyon-Université de Lyon-École normale supérieure - Lyon (ENS Lyon)-Institut de Chimie du CNRS (INC)
Université de Lyon-Université de Lyon-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
École normale supérieure de Lyon (ENS de Lyon)-Université Claude Bernard Lyon 1 (UCBL)
Source :
Journal of Physical Chemistry C, Journal of Physical Chemistry C, American Chemical Society, 2008, 112, pp.10862-10867. ⟨10.1021/jp802416f⟩, Journal of Physical Chemistry C, 2008, 112, pp.10862-10867. ⟨10.1021/jp802416f⟩
Publication Year :
2008
Publisher :
HAL CCSD, 2008.

Abstract

International audience; The adsorption of CO on the two terminations, p(2 × 2) and (√3 × √3) R30°, of the bulk Pt3Sn(111) alloy is studied by high pressure polarization modulation infrared reflection absorption spectroscopy (PM-IRRAS). The influence of O2 is also investigated. While no differences are observed when CO is chemisorbed alone, the behavior of the two terminations clearly differs in presence of O2. The presence of oxygen induces modifications on the (√3 × √3)R30° surface. Finally we study how the interaction between O2 and the surface modifies the reactivity. Hence we show that the p(2 × 2) termination is more efficient than the (√3 × √3) R30° for CO oxidation. However this termination remains more efficient than pure platinum.

Details

Language :
English
ISSN :
19327447 and 19327455
Database :
OpenAIRE
Journal :
Journal of Physical Chemistry C, Journal of Physical Chemistry C, American Chemical Society, 2008, 112, pp.10862-10867. ⟨10.1021/jp802416f⟩, Journal of Physical Chemistry C, 2008, 112, pp.10862-10867. ⟨10.1021/jp802416f⟩
Accession number :
edsair.doi.dedup.....556cf5ace46caa3c65df40e5a9c0321d
Full Text :
https://doi.org/10.1021/jp802416f⟩