Topics in Catalysis

, Volume 57, Issue 1–4, pp 2–13 | Cite as

A Molecular Perspective on the d-Band Model: Synergy Between Experiment and Theory

Original Paper

Abstract

The d-band model of Hammer and Nørskov (Nature 376:238, 1995 [3]) relating adsorption energies to the d-band position, and the adsorption energies to barriers in catalytic reactions, has been extremely successful in predicting reactivities and catalysts. In the present contribution we review recent combined experimental and theoretical work on chemical bond-formation at surfaces. We focus on the adsorbate and how the adsorbate electronic structure can be rehybridized through mixing with unoccupied states to generate the radical state, real or virtual, that can then form electron pairs with the metal d-states, as described by the d-band model. We discuss five important bonding situations: (i) atomic radical, (ii) diatomics with unsaturated π-systems (Blyholder model), (iii) unsaturated hydrocarbons (Dewar–Chatt–Duncanson model), (iv) lone–pair interactions, and (v) saturated hydrocarbons (physisorption). Where the d-band model predicts trends along the series of transition metals, the present work provides intuitive tools for predicting trends among different adsorbates.

Keywords

Chemical bonding Electronic structure X-ray spectroscopy Density functional theory 

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Copyright information

© Springer Science+Business Media New York 2013

Authors and Affiliations

  • Lars Gunnar Moody Pettersson
    • 1
  • Anders Nilsson
    • 2
  1. 1.FYSIKUM, AlbaNova University CenterStockholm UniversityStockholmSweden
  2. 2.SUNCAT Center for Interfacial Chemistry and CatalysisSLAC National Accelerator LaboratoryMenlo ParkUSA

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