Molecular beam study of the mechanism of catalyzed hydrogen–deuterium exchange on platinum single crystal surfaces

Abstract

The hydrogen–deuterium exchange reaction was studied by molecular beam scattering on low and high Miller index crystal faces of platinum in the surface temperature range of 300–1300°K. Under the condition of the experiments which put strict limitation on the residence time of the detected molecules, the reaction product, HD, was readily detectable from the high Miller index, stepped surfaces (integrated reaction probability, defined as total desorbed HD flux divided by D2 flux, is ∼10−1) while HD formation was below the limit of detectability on the Pt(111) low Miller index surface (reaction probability <10−5). Atomic steps at the platinum surface must play a controlling role in dissociating the diatomic molecules. The exchange reaction is first-order in D2 beam pressure and half-order in H2 background pressure. This observation indicates that an atom–molecule reaction or possibly an atom–atom reaction is the rate-limiting step in the exchange. The absence of beam kinetic energy dependence of the rate indicates that the molecular adsorption does not require activation energy. The surface is able to store a sufficiently large concentration of atoms which react with the molecules by a two-branch mechanism. The rate constants for this two-branch mechanism were determined under conditions of constant H atom coverage, reducing the bimolecular reaction to a pseudo-first-order reaction. At lower temperatures (<600°K) the rate constant for the exchange is k1 = (2±1) ×105 exp(−4.5±0.5 kcal/RT) sec−1. The rate determining step appears to be the diffusion of the D2 molecule on the surface to a step site where HD is formed via a three-center (atom–molecule) reaction, or via a two-center (atom–atom) reaction subsequent to D2 dissociation at the step. At higher temperatures (≳600°K) the reaction between an adsorbed H atom and an incident D2 gas molecule competes with the low temperature branch. The rate constant for this branch is k2 = (1±2) ×102 exp(−0.6±0.3 kcal/RT) sec−1. The catalyst action of the platinum surface for the exchange reaction is due to its ability to adsorb and dissociate hydrogen molecules with low activation energy and to store atomic hydrogen on the surface thereby converting the gas phase molecule–molecule reaction to an atom–molecule or atom–atom reaction of low activation energy.