Photocatalytic degradation of selected dyes by titania thin films with various nanostructures

Abstract Titania thin films with various nanostructures of quasi-aligned nanorods, well-aligned nanotubes and nanoparticle aggregates were fabricated and utilized to assist photodegradation of three typical dye derivatives in water, i. e., rhodamine B (RB), methylene blue (MB) and methyl orange (MO). The thin films were characterized by X-ray diffraction, scanning electron microscope and UV–Vis diffuse reflectance spectra. It is found that the bandgap of most lab-fabricated thin films can be estimated more appropriately assuming a direct transition between the valance band and the conduction band of titania. The so-called natural ageing phenomenon was evidence for all the films to assist photodegradation of RB and MB in water; but not discernible for MO, which was much reluctant to photodegradation. MB decomposed much quickly than RB when assisted by titania with predominantly anatase; on the other hand, rutile favored the photodegradation of RB than that of MB. Titania thin films with top morphologies of quasi-aligned nanorods or nanotubes were found to possess advantageous turnover frequency and photonic efficiency over commercial P25 titania and sol–gel derived titania to assist photodegradation of RB and MB in water.