Mechanism of the decomposition of adsorbed methanol over a Pd/α,β-Ga 2O 3 catalyst

Abstract

The thermal decomposition of adsorbed methanol on 2 wt.% Pd/silica, 2 wt.% Pd/gallia and pure gallia, was studied by temperature-programmed surface reaction (TPSR), between 323 and 723 K under He flow, using FT-IR spectroscopy. After methanol adsorption on Pd/silica at 323 K, the concentration of methoxy species on the silica decreased during the TPRS experiment, but some methoxy groups still remained on this support even at 723 K. Simultaneously, methanol decomposed over metallic palladium to yield, stepwise, HCO and CO with the consequent release of H 2 (g). On clean gallia, methanol is Lewis-bound adsorbed to the surface, as well as dissociatively adsorbed as methoxy (CH 3O), but the position of the infrared bands indicates a stronger interaction of these species on gallium oxide than on silica. Methoxy species on gallia are decomposed to (mono- and bi-dentate) formate groups (m- and b-HCOO, respectively) at T > 473 K. We suggest that CO and CO 2 are further produced by non-stoichiometric transformation of these formates, leading to the release of atomic hydrogen on the surface of the oxide, as detected by the Ga H stretching infrared band, and surface anion vacancies. In the presence of Pd on the gallia surface, the dehydrogenation of CH 3O species proceeds faster than over the pure oxide, and we propose the following mechanism for methanol decomposition: (i) methanol reacts with OH groups on the gallia surface to produce water and methoxy species, (ii) the dehydrogenation of the latter carbonaceous group leads to H 2COO, first, and then to m- and b-HCOO, (iii) the hydrogen atoms released in the previous steps are transferred from gallia to the Pd surface where they recombine and desorb as H 2 (g).