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• W2016893003 abstract "A scheme for total electronic energy partitioning within the framework of a one-electron theory of the extended Hückel-type is presented, with a view to extending and augmenting the capabilities of existing theoretical electronic structure analysis tools, specifically overlap population analysis. A total electronic energy partitioning is developed first for molecular and subsequently extended materials. In constructing the partitioning, we define molecular orbital Hamilton populations (MOHP’s) for discrete systems, and Crystal Orbital Hamilton Populations (COHP’s) for extended systems. The various energy partitionings and overlap population analyses are exemplified and contrasted for HX (X=F,Cl,Br), ethane, and a [PtH4]2− polymer. The utility of energy partitioning is demonstrated by effecting a COHP partitioning of the surface–CO interaction for the c(2×2)-CO/Ni(100) chemisorption system. Aspects of the surface–CO interaction less amenable to overlap population analysis are addressed, specifically the role of energetically low-lying filled CO orbitals and the relative contributions of surface s, p, and d bands to surface–CO interaction. Hamilton population analysis leads to a CO (4σ, 5σ)–metal forward donation, metal–CO(2π*) backdonation model for the surface–CO interaction. The metal σ contribution to surface–CO bonding is described as sp dominated metal spd hybrid–CO bonding, modifying slightly the metal d–CO σ bonding model proposed by Blyholder. The metal d-2π* backdonation of the Blyholder model remains. The role of the CO(1π) orbitals is also discussed in the context of CO orbital mixing on binding CO to the Ni(100) surface." @default.
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• W2016893003 date "1999-07-15" @default.
• W2016893003 modified "2023-09-23" @default.
• W2016893003 title "Total energy partitioning within a one-electron formalism: A Hamilton population study of surface–CO interaction in the c(2×2)-CO/ Ni(100) chemisorption system" @default.
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• W2016893003 doi "https://doi.org/10.1063/1.479200" @default.
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