2021 年 129 巻 7 号 p. 453-457
Platinum (Pt) was selectively photodeposited onto zinc rhodium oxide (ZnRh2O4) to serve as a hydrogen (H2)-evolution photocatalyst in a silver (Ag)-inserted ZnRh2O4 and bismuth vanadium oxide (Bi4V2O11) solid-state photocatalyst (ZnRh2O4/Ag/Bi4V2O11). The amount of deposited Pt was controlled by the photodeposition time to generate Pt-loaded ZnRh2O4/Ag/Bi4V2O11 (Pt/ZnRh2O4/Ag/Bi4V2O11) containing up to 0.17 wt % of Pt cocatalyst. The prepared Pt/ZnRh2O4/Ag/Bi4V2O11 photocatalysts were able to catalyze the overall pure-water splitting reaction under irradiation with red light at a wavelength of 700 nm and enhanced the stoichiometric evolution of H2 and O2 from water at Pt amounts exceeding 0.12 wt % of Pt. The apparent quantum efficiency of the water-splitting reaction was highest at 0.17 wt % of Pt. In addition to the loading amount of Pt, the loading of Pt as Pt0 (metallic Pt) is crucial for enhancing the water-splitting activity of Pt/ZnRh2O4/Ag/Bi4V2O11.