Synthesis of Ruthenium-Doped TiO2 Nanotube Arrays for the Photocatalytic Degradation of Terasil Blue Dye

The oxidation of terasil blue dye (TB) has been achieved by photocatalysis under UV light using well organized nanotubes of Ti/TiO2 doped with ruthenium (Ru/Ti/TiO2). Ru/Ti/TiO2 were fabricated by Ti anodization followed by impregnation with 0.04, 0.08 and 0.16 wt% of RuCl3 center dot xH(2)O or KRuO4 as precursor salts. Ti foil anodization was carried out in non-aqueous solutions and in aqueous solutions at pH 7 and pH 12.6. Scanning electron microscopy analyses revealed a morphology of well-defined, organized nanotubes of TVTiO(2)and Ru/Ti/TiO2. The ruthenium was evenly distributed over Ti/TiO2 surface. Cluster formation was also observed for 0.16 wt% Ru loading. The X-ray diffraction spectra showed anatase and rutile phase in pure Ti/TiO(2)and Ru/TVTiO2 nanotubes. Therefore, ruthenium doping did not modify the crystalline phase of Ti/TiO2. Raman spectra did not reveal the rutile phase of TiO2 in the composites which is attributed to the laser characteristics used. The optical band gap energies of the Ti/TiO2 and Ru/TVTiO2 nanotube arrays showed that ruthenium-doping on Ti/TiO2 had slight effect on the band-gap energy. A decrease in the band gap energy of pure Ti/TiO2 (E-g= 2.88 eV) was observed by Ru loading of 0.04 wt% in the Ti/TiO(2 )nanotube arrays (E-g = 2.60 eV). The kinetic rate constant of the photocatalytic oxidation of TB, using 0.08 wt% Ru load, was 1.56 and 1.39 times of that on Ti/TiO2 composite (0.01 min(-1)) synthetized at pH 12.6 impregnated in RuCl3 (0.0156 min(-1)) and KRuO4 (0.0139 min(-1)) solutions, respectively. Nevertheless, the highest rate constant value of TB degradation (87.8%) was 0.0172 min(-1) using 0.16 wt% Ru loading on Ti/TiO2 composite synthetized at pH 7 impregnated in RuCl3; this represents 1.15 times of that on Ti/TiO2 composite (0.0150 min(-1); 81.4% color removal) synthetized under the same conditions.