A theoretical investigation of methane dissociation on Rh(111)

Chak Tong AU*, Meng Sheng Liao, Ching Fai Ng

*Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

21 Citations (Scopus)

Abstract

Methane dissociation (CH4 → CHx + (4 - x) H → C + 4H) over a cluster model of the Rh(111) surface has been investigated using a quasi-relativistic density functional method. The main aim is to evaluate the dissociation energies which may determine catalytic activity of the metal in the partial oxidation of methane to syngas. Dissociative adsorption of methane can be initiated on the Rh surface. However, the abstraction of H from CH4 to produce gas-phase CH3,g radical is energetically unfavorable. This would explain the absence of C2 products. The presence of adsorbed oxygen at an on-top site promotes methane dehydrogenation while that at a hollow site exerts the opposite effect. All calculated dissociation energies of CHx,s are compatible with those obtained with the bond-order conservation Morse-potential approach. The combination and desorption of surface species, which are critical to the formation of syngas, are also discussed.

Original languageEnglish
Pages (from-to)44-50
Number of pages7
JournalChemical Physics Letters
Volume267
Issue number1-2
DOIs
Publication statusPublished - 14 Mar 1997

Scopus Subject Areas

  • Physics and Astronomy(all)
  • Physical and Theoretical Chemistry

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