Reactivity of the Cu2O(100) surface: Insights from first principles calculations

    Authors

    D. Le; S. Stolbov;T. S. Rahman

    Abbreviated Journal Title

    Surf. Sci.

    Keywords

    Ab initio calculations; Density functional theory; Surface structure; Catalysis; Adsorption; Desorption; CO oxidation; DENSITY-FUNCTIONAL THEORY; CARBON-MONOXIDE OXIDATION; TOTAL-ENERGY; CALCULATIONS; AB-INITIO CALCULATIONS; CO OXIDATION; ELECTRONIC-STRUCTURE; METALLIC COPPER; CU2O; OXIDE; ADSORPTION; Chemistry, Physical; Physics, Condensed Matter

    Abstract

    We present a summary of results of systematic first principles calculations of the electronic and geometric structures of the Cu2O(100) surface and the process of CO oxidation on this surface (energetics and pathways of adsorption, diffusion and reactions of CO and O-2 on the surface). The (p, T) phase diagram of the Cu2O(100) in equilibrium of with gas phase O-2. built using the ab initio thermodynamics approach suggests that the O-terminated surface is preferred over the Cu-terminated one within the entire ranges of pressures and temperatures in which the compound exists. Metastable Cu-terminated Cu2O(100) is found to undergo a surface reconstruction in agreement with experiment. We find CO to oxidize spontaneously on the O-terminated Cu2O(100) surface by consuming surface O atoms. Our calculations also show that the surface O-vacancies left in the course of the CO oxidation can be easily filled with dissociative adsorption of the gas phase O-2 molecules, which are usually present in reaction environment. (C) 2009 Elsevier B.V. All rights reserved

    Journal Title

    Surface Science

    Volume

    603

    Issue/Number

    10-12

    Publication Date

    1-1-2009

    Document Type

    Article

    Language

    English

    First Page

    1637

    Last Page

    1645

    WOS Identifier

    WOS:000266786500042

    ISSN

    0039-6028

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