Thermal chemistry of diiodomethane on Ni(1 1 0) surfaces II. Effect of coadsorbed oxygen

Abstract

The effect of coadsorbed oxygen on the thermal chemistry of diiodomethane on Ni(1 1 0) single-crystal surfaces was studied by temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS). I 3d and C 1s XPS data indicated that adsorbed diiodomethane undergoes two sequential C–I bond scission steps to ultimately produce methylene surface species, the same as on clean Ni(1 1 0). Moreover, significant amounts of methane and other heavier hydrocarbons are produced after further thermal activation of those chemisorbed methylene groups. The production of alkanes and alkenes, which is accounted for by a chain growth mechanism where the initial hydrogenation of some adsorbed methylene to methyl moieties is followed by a rate-limiting methylene insertion step to yield ethyl intermediates, is inhibited but not fully blocked by the coadsorbed oxygen. New reaction pathways are also opened up by the presence of oxygen in this system, including a direct coupling of two methylene groups to ethene, the insertion of an oxygen atom into a nickel–methylene group to produce formaldehyde, and a parallel methylene insertion chain growth sequence starting from a CH 2I ads intermediate to ultimately yield C 3H 5 and C 4H 7 unsaturated gas-phase radicals.