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  • 35.20.Dp  (1)
  • chemisorption  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Topics in catalysis 10 (2000), S. 199-207 
    ISSN: 1572-9028
    Keywords: chemisorption ; molecular dynamics ; SEXAFS ; NEXAFS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A useful and necessary step to understand the complexity of catalysis is to first study the simple prototype systems which involve elements active in such reactions. Studies throwing light on gas–metal interaction are of vital importance. The X-ray absorption spectroscopy can provide vital information for catalysis as one probes the system on a very local scale. We present state of the art surface EXAFS measurements of carbon, nitrogen and oxygen adsorbed on well characterised metal surfaces (Ni and Cu). The present contribution highlights from experimental measurements supported by improved theoretical calculations that temperature and angular dependent studies are essential for a reliable structural analysis and to gain an insight into absorbate–substrate bonding and kinetics. The low Z metal systems were found suitable to detect unambiguously the photoelectron backscattering by interstitial charge densities.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 11 (1989), S. 219-229 
    ISSN: 1434-6079
    Keywords: 33.20.Rm ; 33.70.Tg ; 35.20.Dp
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The near edge X-ray absorption fine structure (NEXAFS) at the C K-edge of C2H2, C2H4, C2H6 on Cu(100) and Ag(100) surfaces is studied. The oriented character of the molecules on the surface combined to the dipole selection rules for photon absorption allows an experimental assignment of the nature of the various final states. A careful fitting of the NEXAFS spectra reveals final states of C–H character and shake-up satellites of the C(1 s) to π* (C–C) transition. The asymmetric line shape of the C(1 s) to σ* (C–C) transition is described in a scattering model of the photoelectron from the molecular potential.
    Type of Medium: Electronic Resource
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