Vertically aligned rutile TiO2 nanowire arrays (NWAs) with lengths of ∼44 μm have been successfully synthesized on transparent, conductive fluorine-doped tin oxide (FTO) glass by a facile one-step solvothermal method. The length and wire-to-wire distance of NWAs can be controlled by adjusting the ethanol content in the reaction solution. By employing optimized rutile TiO2 NWAs for dye-sensitized solar cells (DSCs), a remarkable power conversion efficiency (PCE) of 8.9% is achieved. Moreover, in combination with a light-scattering layer, the performance of a rutile TiO2 NWAs based DSC can be further enhanced, reaching an impressive PCE of 9.6%, which is the highest efficiency for rutile TiO2 NWA based DSCs so far.

Zn-doped SnO2 nanocrystals were successfully synthesized by a simple hydrothermal method. It is found that Zn doping into SnO2 can induce a negative shift in the flat-band potential (VFB) and increase the isoelectric point. As a result, dye-sensitized solar cells (DSCs) based on Zn-doped SnO2 nanocrystal photoanodes exhibit longer electron lifetimes and higher dye loading compared to undoped SnO2 based DSCs. The overall power conversion efficiency (η) of the optimized Zn-doped SnO2 based DSC reaches 4.18% and increases to 7.70% after the TiCl4 treatment. More importantly, a remarkable η of 8.23% is achieved for DSCs based on a high-quality double-layer SnO2 photoanode with the TiCl4 treatment, to the best of our knowledge, which is so far the best reported efficiency for DSCs based on SnO2 photoanodes.

A novel self-powered UV photodetector (UVPD) based on the photoelectrochemical cell (PECC) has been constructed using the TiO2 coated SnO2 mesoporous spheres (SnO2-MS@TiO2). This self-powered UVPD displays a higher photocurrent density compared to the UVPD with the pure SnO2-MS. By means of external quantum efficiency (EQE), UV-vis absorption, and electrochemical impedance measurements, we scrutinize the intrinsic role of the TiO2 coating layer on the photocurrent enhancement. Under UV irradiation, this UVPD exhibits a high on/off ratio of 11519, a fast rise time of 0.007 s and decay time of 0.006 s, together with the excellent visible-blind characteristic and linear optical signal response. The self-powered photodetector is a promising candidate for application in high-sensitivity and high-speed UVPDs.

The anatase and rutile phases existing in commercially available P25 powder were separated according to their different particle size and chemical affinity. Firstly, electrical double layer was established on TiO2 surface to achieve a highly dispersed TiO2 colloid due to electrostatic repulsive forces. Additionally, strong electrolyte HCl was added to neutralize the weak electrical double layer of rutile particles, and makes them precipitated from TiO2 colloid priorly by centrifugal force. As the amount of HCl increased from 0 to 2 ml, the anatase percent increased from 83.2 to 100%, the diameter decreased from 30.0 to 19.7 nm while the specific surface increased from 52.9 to 76.3 m2/g. Further, the conversion efficiency of dye-sensitized solar cells fabricated from the separated powder increased from 8.52 to 10.1% under 100 mW cm−2 AM 1.5 illumination.

Zn-doped SnO2 nanocrystals were successfully synthesized by a simple hydrothermal method. It is found that Zn doping into SnO2 can induce a negative shift in the flat-band potential (VFB) and increase the isoelectric point. As a result, dye-sensitized solar cells (DSCs) based on Zn-doped SnO2 nanocrystal photoanodes exhibit longer electron lifetimes and higher dye loading compared to undoped SnO2 based DSCs. The overall power conversion efficiency (η) of the optimized Zn-doped SnO2 based DSC reaches 4.18% and increases to 7.70% after the TiCl4 treatment. More importantly, a remarkable η of 8.23% is achieved for DSCs based on a high-quality double-layer SnO2 photoanode with the TiCl4 treatment, to the best of our knowledge, which is so far the best reported efficiency for DSCs based on SnO2 photoanodes.