• Title of article

    The chemistry of ethylene on MoAl alloy thin films formed on dehydroxylated alumina: Hydrogenation, dehydrogenation and H–D exchange reactions

  • Author/Authors

    Gao، نويسنده , , Feng and Wang، نويسنده , , Yilin and Burkholder، نويسنده , , Luke and Tysoe، نويسنده , , W.T.، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 2006
  • Pages
    12
  • From page
    1837
  • To page
    1848
  • Abstract
    The chemistry of ethylene adsorbed on a thin MoAl layer grown in ultrahigh vacuum on a thin alumina film is studied using a combination of temperature-programmed desorption and X-ray, Auger and reflection absorption infrared spectroscopies. Both di-σ-bonded and a small proportion of π-bonded ethylene are found, where the di-σ-bonded ethylene has a σ/π parameter of ∼0.8 and a heat of adsorption of ∼70 kJ/mol. The ethylene self-hydrogenates to yield ethane and a small amount of methane is detected. The surface hydrogenation activation energy of di-σ-bonded ethylene is ∼65 kJ/mol, while the π-bonded species hydrogenates more easily. Adsorbed ethyl species grafted onto the surface by decomposing ethyl iodide predominantly undergo β-hydride elimination to yield ethylene. Ethyl species hydrogenate to ethane at a lower temperature than does di-σ-bonded ethylene implying that addition of hydrogen to adsorbed ethylene is slower than the rate of ethyl hydrogenation.
  • Keywords
    Chemisorption , Iodoethane , Alumina thin films , X-ray photoelectron spectroscopy , Temperature-programmed desorption , Auger spectroscopy , ethylene , Reflection–absorption infrared spectroscopy , Molybdenum hexacarbonyl
  • Journal title
    Surface Science
  • Serial Year
    2006
  • Journal title
    Surface Science
  • Record number

    1698188