Issue 3, 1992

Time-dependent chemiluminescence from the surface-catalysed recombination of O and NO on polycrystalline platinum

Abstract

The chemiluminescence produced by the surface-catalysed recombination of nitric oxide with a supersonic beam of atomic oxygen on polycrystalline platinum has been studied. The dependence of the luminescence on time, substrate temperature, O and NO fluxes and pre-exposure to the O-atom beam has been investigated. An initial luminescent signal was observed which decayed with time to a steady state. The initial luminescent intensity at any given temperature was less than the signal observed previously on a nickel sample, and it is suggested that this arises from the different adsorption characteristics of NO, O2 and electronically excited NO2 on the two surfaces. Also apparent was a ‘fast’ decay in the luminescence for temperatures at or below 220 K, which lasts for only a few seconds before the reaction proceeds by a slower decay process. This fast decay, which was not detected on nickel, may arise from the initial reaction of chemisorbed O atoms on the oxidised platinum surface with NO. The mechanism proposed previously has been used to determine the rate constants of the reaction.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans., 1992,88, 399-404

Time-dependent chemiluminescence from the surface-catalysed recombination of O and NO on polycrystalline platinum

M. H. P. Ardebili, R. Grice, C. J. Hughes and J. C. Whitehead, J. Chem. Soc., Faraday Trans., 1992, 88, 399 DOI: 10.1039/FT9928800399

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