Surface Reconstruction-Induced Photocatalytic Methanol Reduction Reaction on a Rutile TiO2(001) Surface

Photochemistry of methanol on TiO2 surfaces is of great importance both fundamentally and industrially. Methanol was previously reported only to occur photogenerated hole-participating oxidation reactions on TiO2 surfaces. Herein, we report that, upon UV light illumination, the methoxy species formed by methanol dissociation at the 5-fold coordinated Ti4+ sites (CH3O(a)(Ti5c)) of a reconstructed rutile TiO2(001)-(1 x 1) surface also undergoes the C-O bond cleavage into methyl fragments mediated by photogenerated electrons, in addition to the well-established photogenerated hole-participating oxidation reactions. Upon subsequent heating, the resulting methyl species undergoes hydrogenation and coupling reactions into methane and ethane, respectively. Accompanying theoretical calculations showed that the lowest unoccupied molecular orbital (LUMO) of CH3O(a)(Ti5c) is localized almost at the conduction band minimum of the CH3O-adsorbed reconstructed rutile TiO2(001)-(1 x 1) surface, indicating the likely TiO2 -> CH3O(a)(Ti5c) interfacial photoexcited-electron transfer. These results greatly broaden the photochemistry of methanol on TiO2 surfaces and demonstrate a photocatalytic methanol-to-hydrocarbon reaction route.