Transformation of hydrogen titanate nanoribbons to TiO(2) nanoribbons and the influence of the transformation strategies on the photocatalytic performance

The influence of the reaction conditions during the transformation of hydrogen titanate nanoribbons to TiO(2) nanoribbons on the phase composition, the morphology, the appearance of the nanoribbon surfaces and their optical properties was investigated. The transformations were performed (i) through a heat treatment in oxidative and reductive atmospheres in the temperature range of 400–650 °C, (ii) through a hydrothermal treatment in neutral and basic environments at 160 °C, and (iii) through a microwave-assisted hydrothermal treatment in a neutral environment at 200 °C. Scanning electron microscopy investigations showed that the hydrothermal processing significantly affected the nanoribbon surfaces, which became rougher, while the transformations based on calcination in either oxidative or reductive atmospheres had no effect on the morphology or on the surface appearance of the nanoribbons. The transformations performed in the reductive atmosphere, an NH(3)(g)/Ar(g) flow, and in the ammonia solution led to nitrogen doping. The nitrogen content increased with an increasing calcination temperature, as was determined by X-ray photoelectron spectroscopy. According to electron paramagnetic resonance measurements the calcination in the reductive atmosphere also resulted in a partial reduction of Ti(4+) to Ti(3+). The photocatalytic performance of the derived TiO(2) NRs was estimated on the basis of the photocatalytic oxidation of isopropanol. After calcinating in air, the photocatalytic performance of the investigated TiO(2) NRs increased with an increased content of anatase. In contrast, the photocatalytic performance of the N-doped TiO(2) NRs showed no dependence on the calcination temperature. An additional comparison showed that the N-doping significantly suppressed the photocatalytic performance of the TiO(2) NRs, i.e., by 3 to almost 10 times, in comparison with the TiO(2) NRs derived by calcination in air. On the other hand, the photocatalytic performance of the hydrothermally derived TiO(2) NRs was additionally improved by a subsequent heat treatment in air.