The photochemistry of CH

R. Larciprete, A. Goldoni, A. Groŝo, S. Lizzit, G. Paolucci

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Abstract

The photochemistry induced at 40 K by synchrotron radiation at 400 eV in CH4molecules adsorbed on Pt(1 1 1) was studied by high resolution fast XPS. The photoreactions were monitored by acquiring the C1s core level spectrum as a function of time for methane adlayers with coverage ranging from submonolayer to multilayer regime. We have observed molecular desorption of the multilayer and effective dissociation in the layer in contact with the metal. Differently from UV photons and low energy e-beam induced dissociation of CH4adsorbed on Pt(1 1 1) - which only produced adsorbed CH3and H fragments - the C1s core level measured on methane photodissociated at 400 eV shows that other species are formed, which start to thermally dissociate at about 100 K, producing CH and possibly H. Probable candidates are CH2, formed by multiple C-H bond cleavage together with CH3groups during the initial methane photodissociation, or a C-C containing intermediate, resulting from methyl surface chemistry. © 2001 Elsevier Science B.V.
Original languageEnglish
Pages (from-to)134 - 140
Number of pages7
JournalSurface Science
Volume482-485
Issue numberPART 1
DOIs
Publication statusPublished - 20 Jun 2001
Externally publishedYes

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All Science Journal Classification (ASJC) codes

  • Condensed Matter Physics
  • Surfaces and Interfaces
  • Surfaces, Coatings and Films
  • Materials Chemistry

Cite this

Larciprete, R., Goldoni, A., Groŝo, A., Lizzit, S., & Paolucci, G. (2001). The photochemistry of CH. Surface Science, 482-485(PART 1), 134 - 140. https://doi.org/10.1016/S0039-6028(01)00758-0