Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 113, Issue 40, Pages 17536-17542Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jp907128k
Keywords
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Funding
- Chemistry of Concerto Catalysis [20037061]
- MEXT Japan [460]
- ENEOS Hydrogen Trust Fund
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Ru/SrTiO3:Rh photocatalyst powder for H-2 evolution and varied photocatalyst powders for O-2 evolution Such as BiVO4 and WO3 were suspended in acidified aqueous solutions. resulting in showing activities for water splitting into H-2 and O-2 in a stoichiometric ratio without an electron mediator under visible light irradiation. The photocatalytic activities were dependent oil pH. The highest activity was obtained at pH 3.5. An optical microscope observation of the aqueous Suspension containing Ru/SrTiO3:Rh and BiVO4 powders at pH 3.5 revealed that these powders aggregated with suitable contact. The condition of Rh doped in SrTiO3 also affected strongly the photocatalytic activity and quenching of the photoluminescence of BiVO4. The high photocatalytic activity was obtained and the luminescence was remarkably quenched, when SrTiO3:Rh containing, Rh species with reversible redox properties was used and mixed. These results indicated that the photocatalytic water splitting and quenching of the photoluminescence Occurred through interparticle electron transfer from the conduction band of BiVO4 to impurity level consisting of the reversible Rh species doped in SrTiO3. Thus, We Succeeded in constructing unique and simple Z-scheme photocatalysis systems driven by interparticle electron transfer under visible light irradiation. In addition, the (Ru/SrTiO3:Rh)-(BiVO4) system split water under simulated Sunlight (AM-1.5).
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