The coadsorption of ammonia and oxygen on Ni{110}: a RAIRS study

H. E. Dastoor, P. Gardner, D. A. King

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The adsorption of NH3 on clean Ni{110} and Ni{110} preexposed with oxygen has been investigated in the temperature range 150 to 300 K using high resolution infrared spectroscopy (RAIRS). Prior to saturation on the clean surface at 150 K, ammonia adsorbs into atop sites, giving a symmetric deformation (umbrella) mode frequency of 1122 cm-1 (0.55%), FWHM = 17 cm-1 [867 cm-1 (0.25%), FWHM = 11 cm-1 for ND3]. A second band, which is fully resolved for ND3, where the bands are narrowe in as saturation is approached, and is assigned to adsorption on bridge sites. The NH3/O system exhibits a more complex behaviour, with at least four vibrationally distinct surface ammonia species in the oxygen coverage range 0-0.5 ML. Surface structures as seen by STM in the literature are used to aid assignment of the infrared bands. On the regular p(3 × 1) and p(2 × 1) surfaces ammonia adsorbs onto strongly perturbed atop sites on Ni-O chains. On both these surfaces ammonia is also adsorbed on second layer sites between the chains, at atop sites on the p(3 × 1) surface, but due to a higher Ni-O chain density, at less stable bridge sites on the p(2 × 1) surface. We propose that dissociation of ammonia occurs only on the low coverage oxygen phase, θo <0.3 ML, and that dissociation depends upon an optimum orientation rather than simply upon the strength of the interaction of NH3 with the surface. © 1993.
    Original languageEnglish
    Pages (from-to)279-289
    Number of pages10
    JournalSurface Science
    Volume289
    Issue number3
    Publication statusPublished - 1 Jun 1993

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