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A composited system was fabricated by coupling Pt/TiO2 with water-splitting catalyst for photooxidation of organic pollutants in aqueous solutions. The new composited system exhibits more efficient photocatalytic activity than pure Pt/TiO2 does under UV light irradiation. The promoting effect is dependent on the photo-produced H2 over the composited system. The active oxygen species, hydroxyl radical (·OH) and hydrogen peroxide (H2O2), are measured by fluorescence spectroscopy and photometric method, respectively. The results reveal that the produced H2 by photocatalytic water splitting over NiO/NaTaO3:La transfers to Pt particle of TiO2 surface, then reacts with introducing O2 to generate in situ intermediate H2O2, and finally translates into ·OH radical to accelerate the photooxidation of organic pollutants. [ABSTRACT FROM AUTHOR]

A composited system was fabricated by coupling Pt/TiO2 with water-splitting catalyst for photooxidation of organic pollutants in aqueous solutions. The new composited system exhibits more efficient photocatalytic activity than pure Pt/TiO2 does under UV light irradiation. The promoting effect is dependent on the photo-produced H2 over the composited system. The active oxygen species, hydroxyl radical (·OH) and hydrogen peroxide (H2O2), are measured by fluorescence spectroscopy and photometric method, respectively. The results reveal that the produced H2 by photocatalytic water splitting over NiO/NaTaO3:La transfers to Pt particle of TiO2 surface, then reacts with introducing O2 to generate in situ intermediate H2O2, and finally translates into ·OH radical to accelerate the photooxidation of organic pollutants. [ABSTRACT FROM AUTHOR]

The C-doped CdO photocatalysts were simply prepared by high-temperature solid-state process. The as-prepared photocatalysts were characterized by X-ray powder diffraction (XRD), diffuse reflectance spectroscopy (UV-Vis DRS), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The results demonstrated that the carbon was doped into CdO, resulting in the red-shift of the optical absorption of CdO. The photocatalytic behavior of CdO and C-doped CdO was evaluated under the visible light irradiation by using the photocatalytic hydrogen evolution as a model reaction. The C-doped CdO photocatalysts had higher photocatalytic activity over parent CdO under visible light irradiation. The results indicated that the H2 production was due to the existence of CdS and the enhancement of visible light photocatalytic activity of H2 production was originated from the doping of carbon into the CdO lattice. The probably reaction mechanism was also discussed and proposed. [ABSTRACT FROM AUTHOR]