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Highly ordered sodium-free titanate nanotube films were one-step prepared on F-doped SnO2-coated (FTO) glass via an electrophoretic deposition method by using sodium titanate nanotubes as the precursor. It was found that the self-assembled formation of highly ordered sodium titanate nanotube films was accompanied with the effective removal of sodium ions in the nanotubes during the electrophoretic deposition process, resulting in the final formation of protonated titanate nanotube film. With increasing calcination temperature, the amorphous TiO2 phase is formed by a dehydration process of the protonated titanate nanotubes at 300°C and further transforms into anatase TiO2 when the calcination temperature is higher than 400°C. Compared with the as-prepared titanate nanotube film, the calcined titanate nanotube film (300–600°C) exhibits attractive photoinduced superhydrophilicity under UV-light irradiation. In particular, 500°C-calcined films show the best photoinduced superhydrophilicity, probably due to synergetic effects of enhanced crystallization, surface roughness, and ordered structures of the films.

Mesoporous Au-TiO2 nanocomposite plasmonic photocatalyst with visible-light photoactivity was prepared by a simple spray hydrolytic method using photoreduction technique at 90∘C. The prepared samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and N2 adsorption-desorption isotherms. The formation of hydroxyl radicals (•OH) on the surface of visible-light illuminated Au-TiO2 nanocomposites was detected by the luminescence technique using terephthalic acid as probe molecules. The photocatalytic activity was evaluated by photocatalytic decolorization of Rhodamine-B (RhB) aqueous solution under visible-light irradiation (λ > 420 nm). The results revealed that the TiO2 could be crystallized via spray hydrolysis method, and the photoreduction technique was facilitated to prepare Au nanoparticles in the mesoporous TiO2 at 90∘C. The light absorption, the formation rate of hydroxyl radicals, and photocatalytic decolorization of Rhodamine-B aqueous solution were significantly enhanced by those embedded Au nanoparticles in the Au-TiO2 nanocomposites. The prepared Au-TiO2 nanocomposites exhibit a highly visible-light photocatalytic activity for photocatalytic degradation of RhB in water, and their photocatalytic activity is higher than that of the pristine TiO2 nanoparticles due to the surface plasmon resonance.

Mesoporous Au-TiO2 nanocomposite plasmonic photocatalyst with visible-light photoactivity was prepared by a simple spray hydrolytic method using photoreduction technique at 90°C. The prepared samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and N2 adsorption-desorption isotherms. The formation of hydroxyl radicals (• OH) on the surface of visible-light illuminated Au-TiO2 nanocomposites was detected by the luminescence technique using terephthalic acid as probe molecules. The photocatalytic activity was evaluated by photocatalytic decolorization of Rhodamine-B (RhB) aqueous solution under visible-light irradiation (λ > 420 nm). The results revealed that the TiO2 could be crystallized via spray hydrolysis method, and the photoreduction technique was facilitated to prepare Au nanoparticles in the mesoporous TiO2 at 90°C. The light absorption, the formation rate of hydroxyl radicals, and photocatalytic decolorization of Rhodamine-B aqueous solution were significantly enhanced by those embedded Au nanoparticles in the Au-TiO2 nanocomposites. The prepared Au-TiO2 nanocomposites exhibit a highly visible-light photocatalytic activity for photocatalytic degradation of RhB in water, and their photocatalytic activity is higher than that of the pristine TiO2 nanoparticles due to the surface plasmon resonance. [ABSTRACT FROM AUTHOR]