Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/9825
Title: Theoretical analysis of the bonding of oxygen to Cu(100)
Author: Bagus, Paul S.
Illas i Riera, Francesc
Keywords: Química de superfícies
Orbitals atòmics
Surface chemistry
Atomic orbitals
Issue Date: 1990
Publisher: The American Physical Society
Abstract: The chemisorption of O/Cu(100) has been modeled by a Cu 5 O cluster; ab initio self-consistent-field electronic wave functions have been obtained for this cluster. The bonding has been analyzed using several new theoretical methods: (1) the variation of the Cu 5 O dipole moment with the distance of O from the surface; (2) the projection of the O orbitals from Cu 5 O; and (3) the constrained space orbital variation (CSOV) method for the development of the bond. It is concluded that the bond is dominantly ionic but with a significant covalent contribution. Our results indicate that the excess charge on O is ∼1.5 electrons. We have computed the CSOV analysis for Cu 5 O and for Cu 5 with point charges. The comparison of these two clusters has allowed us to have a definitive measure of the contribution of the Cu d electrons to the covalent bond. The total contribution of the d electrons to the bond is rather large (1.2 eV). Once the different contributions are separated, it is shown that purely electrical polarization effects account for ∼0.5 eV, while the direct participation of the d electrons in the covalent bond is ∼0.7 eV.
Note: Reproducció digital del document publicat en format paper, proporcionada per PROLA i http://dx.doi.org/10.1103/PhysRevB.42.10852
It is part of: Physical Review B, 1990, vol. 42, núm. 17, p. 10852-10857.
Related resource: http://dx.doi.org/10.1103/PhysRevB.42.10852
URI: http://hdl.handle.net/2445/9825
ISSN: 0163-1829
Appears in Collections:Articles publicats en revistes (Ciència dels Materials i Química Física)

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