Abstract
The structure and reactivity of a series of Pt(111)/ceria model catalysts have been studied as a function of ceria coverage and morphology. XPS and LEED data show that the method of preparation results in growth of disordered CeO2 which converts to epitaxial (111)-oriented ceria upon annealing at >700 K. Submonolayer ceria coverages strongly promote the oxidation of CO. Most strikingly, the fully encapsulated Pt(111) wafer is a much more effective catalyst than the barc metal itself. Disordered encapsulating films are much more active than ordered films. The results are discussed in terms of Pt-promoted oxygen vacancy formation in ceria and the predicted relative reactivity of principal crystal faces of the oxide.
Original language | English |
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Pages (from-to) | 10901-10905 |
Number of pages | 5 |
Journal | Journal of Physical Chemistry |
Volume | 98 |
Issue number | 42 |
Publication status | Published - 1 Jan 1994 |