High surface area, amorphous titania with reactive Ti3+ through a photo-assisted synthesis method for photocatalytic H2 generation

Abstract

Amorphous titania-based photocatalysts are synthesized using a facile, UV-light mediated method and evaluated as photocatalysts for hydrogen evolution from water/methanol mixtures. The photocatalysts are prepared through the direct injection of a titanium alkoxide precursor into a water/methanol mixture, with subsequent hydrolysis, condensation, and polycondensation to form TiO_x(OH)_y species under UV-irradiation. The resulting amorphous titania materials exhibit an overall higher hydrogen evolution rate compared to a crystalline TiO₂ reference (P25) on a molar basis of the photocatalyst due to their highly porous structure and high surface area (∼500 m² g⁻¹). The employed titanium alkoxide precursor did not play a major role in affecting the hydrogen evolution rate or the catalyst surface and morphology. A blue coloration, which is associated with the formation of Ti³⁺ species, was observed in the amorphous titania but not in P25 upon light irradiation and is enabled by the porous and disordered structure of the amorphous photocatalyst. The Ti³⁺ species are also used to reduce protons to H₂ in the absence of light irradiation or reduce Pt²⁺ to form Pt nanoparticles. These Pt nanoparticles are smaller and better dispersed on the photocatalyst compared to particles prepared using conventional photodeposition, leading to higher H₂ evolution rates. The results show that the direct injection method is a facile approach for the preparation of high surface area titania photocatalysts containing Ti³⁺ species with good photocatalytic activity for the production of H₂.