Sensitization of Pt/TiO₂ using plasmonic Au nanoparticles for hydrogen evolution under visible-light irradiation

Au nanoparticles with different sizes (10, 20, 30, and 50 nm) were synthesized using a seed-assisted approach and anchored onto Pt/TiO₂ employing 3-mercaptopropionic acid as the organic linker. The sizes of the Au nanoparticles were controlled within a narrow range so that the size-dependent surface plasmonic resonance effect on sensitizing Pt/TiO₂ can be thoroughly studied. We found that 20 nm Au nanoparticles (Au₂₀) gave the best performance in sensitizing Pt/TiO₂ to generate H₂ under visible-light illumination. Photoelectrochemical measurements indicated that Au₂₀-Pt/TiO₂ exhibited the most efficient "hot" electrons separation among the studied catalysts, correlating well with the photocatalytic activity. The superior performance of Au-supported Pt/TiO₂ (Au₂₀-Pt/TiO₂) compared with Au anchored to TiO₂ (Au₂₀/TiO₂) revealed the important role of Pt as a cocatalyst for proton reduction. To elucidate how the visible-light excited hot electrons in Au nanoparticles involved in the proton-reduction reaction process, Au₂₀/TiO₂ was irradiated by visible light (λ > 420 nm) with the presence of Pt precursor (H₂PtCl₆) in a methanol aqueous solution under deaerated condition. Energy-dispersive X-ray spectroscopy mapping analysis on the recovered sample showed that Pt ions could be reduced on the surfaces of both Au nanoparticles and TiO₂ support. This observation indicated that the generated hot electrons on Au nanoparticles were injected into the TiO₂ conduction band, which were then subsequently transferred to Pt nanoparticles where proton reduction proceeded. Besides, the excited hot electrons could also participate in the proton reduction on Au nanoparticles surface.