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CO adsorption on clean and oxidized Pt3Ti(111)
Authors:Séverine Le Moal  Marco Moors  Jan Markus Essen  Conrad Becker  Klaus Wandelt
Institution:1. Institute of Physical and Theoretical Chemistry, University of Bonn, Wegelerstraße 12, D-53115 Bonn, Germany;2. Centre Interdisciplinaire de Nanoscience de Marseille, CNRS — UPR 3118, Université de la Méditerranée and Université Paul Cézanne, Campus de Luminy, Case 913, F-13288 Marseille Cedex 09, France
Abstract:CO adsorption on clean and oxidized Pt3Ti(111) surfaces has been investigated by means of Auger Electron Spectroscopy (AES), Thermal Desorption Spectroscopy (TDS), Low Energy Electron Diffraction (LEED) and High Resolution Electron Energy Loss Spectroscopy (HREELS). On clean Pt3Ti(111) the LEED patterns after CO adsorption exhibit either a diffuse or a sharp c(4 × 2) structure (stable up to 300 K) depending on the adsorption temperature. Remarkably, the adsorption/desorption behavior of CO on clean Pt3Ti(111) is similar to that on Pt(111) except that partial CO decomposition on Ti sites and partial CO oxidation have also been evidenced. Therefore, the clean surface cannot be terminated by a pure Pt plane. Partially oxidized Pt3Ti(111) surfaces (< 135 L O2 exposure at 1000 K) exhibit a CO adsorption/desorption behavior rather similar to that of the clean surface, showing again a c(4 × 2) structure (stable up to 250 K). Only the oxidation of CO is not detectable any more. These results indicate that some areas of the substrate remain non-oxidized upon low oxygen exposures. Heavily oxidized Pt3Ti(111) surfaces (> 220 L O2 exposure at 1000 K) allow no CO adsorption indicating that the titanium oxide film prepared under these conditions is completely closed.
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