Ab initio cluster model approach to the chemisorption of NH 3 on Pt(111)

Abstract

The chemisorption of NH 3 on Pt(111) has been studied using several Pt 10 clusters that model different adsorption sites of the Pt(111) surface. Ab initio methods have been used to obtain a theoretical estimate of several spectroscopic features that can be directly compared to experiment. The comparison includes the variation of the difference between the 3a 1 and 1e levels, the vibrational frequency shifts and the order of stability on different surface sites. Chemisorption at the on-top site is predicted to be favoured, the calculated interaction energy appears to be quite close to the experimental estimate, and it is suggested that NH 3 chemisorbs molecularly, in an N-down orientation, with an equilibrium geometry representing a small distortion from the gas-phase molecular geometry and no azimuthal preference, in good agreement with ESDIAD experiments. Constrained space orbital variation (CSOV) analysis of the interaction has also been performed using a Hartree–Fock wave function. This analysis shows that the leading bonding mechanisms are substrate polarisation and charge transfer from ammonia to the surface.