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In this study, a self-organized nanotubular titanium dioxide (TiO2) array was successfully produced by anodizing pure titanium in a mixture of glycerol, distilled water (8% vol.), and ammonium fluoride using a dual electrode system. The size control and distribution of the nanopores were performed in a DC voltage range varying from 30 V to 60 V. The diameter of TiO2 nanopores varies from 59 to 128 nm depending on the anodizing voltage. Energy-dispersive X-ray spectroscopy (EDX) analysis reveals that the as-prepared films are essentially composed of TiO2. According to the X-ray diffraction (XRD) and Raman spectroscopy analysis, the nanotubular arrays of TiO2 annealed at 600°C for 2 hours are composed of a phase mixture of anatase and rutile. Mott-Schottky analysis showed that the TiO2 nanotubes are consistent with an n-type semiconductor with a donor density of about 1017 cm-3. Preliminary results on the photocatalytic degradation of a pharmaceutical pollutant showed that the TiO2 nanotubes can be used as a promising material for application in wastewater treatment.

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The anodization of the Ti-Cu (2%) alloy was carried out in a 5M H3PO4 solution for 2 minutes. The obtained layers are characterized by XPS, X-ray diffraction, and Raman spectroscopy. The results showed that the obtained films are composed of poorly crystallized TiO2 oxide. Electrochemical Impedance spectroscopy studies revealed that the thickness of the formed film increases with increasing anodization potential. Additionally, the resistance of charge transfer becomes higher when the anodization potential increases. Thus, the Mott Schottky model revealed that the formed film is an n-type semiconductor. The density of charge carriers is in good agreement with those found in the literature. Also, it is found that the flat-band potential increases with increasing treatment potential.

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