Photocatalytic H2 Production Using Pt-TiO2 in the Presence of Oxalic Acid: Influence of the Noble Metal Size and the Carrier Gas Flow Rate

Abstract

The primary objective of the experiments was to investigate the differences in the photocatalytic performance when commercially available Aeroxide P25 TiO₂ photocatalyst was deposited with differently sized Pt nanoparticles with identical platinum content (1 wt%). The noble metal deposition onto the TiO₂ surface was achieved by <i>in situ</i> chemical reduction (CRIS) or by mixing chemically reduced Pt nanoparticle containing sols to the aqueous suspensions of the photocatalysts (sol-impregnated samples, CRSIM). Fine and low-scale control of the size of resulting Pt nanoparticles was obtained through variation of the trisodium citrate concentration during the syntheses. The reducing reagent was NaBH₄. Photocatalytic activity of the samples and the reaction mechanism were examined during UV irradiation (λ_max = 365 nm) in the presence of oxalic acid (50 mM) as a sacrificial hole scavenger component. The H₂ evolution rates proved to be strongly dependent on the Pt particle size, as well as the irradiation time. A significant change of H₂ formation rate during the oxalic acid transformation was observed which is unusual. It is probably regulated both by the decomposition rate of accumulated oxalic acid and the H⁺/H₂ redox potential on the surface of the catalyst. The later potential is influenced by the concentration of the dissolved H₂ gas in the reaction mixture.