Adsorbate ionicity and surface-dipole-moment changes: Cluster-model studies of Cl/Cu(100) and F/Cu(100)
- 3 February 1986
- journal article
- research article
- Published by American Physical Society (APS) in Physical Review Letters
- Vol. 56 (5), 500-503
- https://doi.org/10.1103/physrevlett.56.500
Abstract
A cluster-model study of Cl and F chemisorbed at a fourfold site of Cu(100) shows that the halogen ionicity is essential -1. The interaction and bonding arise, almost entirely, from the Coulomb attraction between the charged halogen and metal and from the polarization of the electrons associated with these units; covalent bonding makes a very small contribution. The polarization dramatically reduces the dipole moment from that given by the unpolarized ionic units. Thus, changes in the work function are not a measure of the adsorbate ionicity.Keywords
This publication has 15 references indexed in Scilit:
- Chemical bonding effects in the inverse photoemission spectra of chemisorbed COChemical Physics Letters, 1985
- Reactivity of coordinated nucleophiles toward cis migration in (.pi.-olefin)palladium complexesJournal of the American Chemical Society, 1984
- Bonding of CO to metal surfaces: A new interpretationPhysical Review B, 1983
- Effective core potential calculations using frozen orbitals. Applications to transition metalsChemical Physics, 1983
- Ab initiocluster study of the interaction of fluorine and chlorine with the Si(111) surfacePhysical Review B, 1983
- Geometry and Electronic Structure of Cl on the Cu {001} SurfacePhysical Review Letters, 1982
- Atomic structure of Cu{0 0 1}c(2 × 2)-ClSolid State Communications, 1982
- Molecular-orbital cluster-model study of the core-level spectrum of CO adsorbed on copperPhysical Review B, 1981
- Chemisorption and incorporation of oxygen at a nickel surfaceProceedings of the Royal Society of London. Series A. Mathematical and Physical Sciences, 1967
- Single determinant wave functionsProceedings of the Royal Society of London. Series A. Mathematical and Physical Sciences, 1961