Title

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

Authors

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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