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TiO_2 rutile/anatase heterostructure thin films with varying rutile thickness have been in-situ synthesized via DC magnetron sputtering with Ar gas at room temperature. The crystal texture, surface morphology, energy gap and optical properties of the films have been investigated by X-ray diffraction meter, grazing incidence X-ray diffraction meter, Raman spectroscopy, scanning electron microscopy, and UV–visible spectrophotometer, which indicates that the rutile/anatase heterostructure films are successfully fabricated. The further degradation experiments display that the photocatalytic activity can be dramatically affected by the thickness of the outmost rutile layer and the 100 nm thickness exhibits the best performance in all of the TiO_2 thin films. With the increase of the outmost rutile layer, the optical band gap of TiO_2 film displays a systematic decrease slightly. However,the change in photocatalytic activity does not coincide with that in the band gap. The photoresponse and electrochemical properties of the thin films have been characterized to understand the mechanism of the varied photocatalytic activity.
TiO_2 rutile / anatase heterostructure thin films with varying rutile thickness have been in-situ synthesized via DC magnetron sputtering with Ar gas at room temperature. The crystal texture, surface morphology, energy gap and optical properties of the films have been investigated by X-ray diffraction meter, grazing incidence X-ray diffraction meter, Raman spectroscopy, scanning electron microscopy, and UV-visible spectrophotometer, which indicates that the rutile / anatase heterostructure films are successfully fabricated. The further degradation experiments display that the photocatalytic activity can be affected as by the thickness of the outmost rutile layer and the 100 nm thickness exhibits the best performance in all of the TiO 2 thin films. With the increase of the outmost rutile layer, the optical band gap of TiO 2 film displays a systematic decrease slightly. However, the change in photocatalytic activity does not coincide with that in the band gap. The photoresponse an d electrochemical properties of the thin films have been to to understand the mechanism of the varied photocatalytic activity.