Enhanced photocatalytic properties of band structure engineered Pd/TiO2 via sequential doping

Band structure engineering is an essential and promising approach for altering photocatalytic properties of TiO2 for enhanced H-2 production and dye degradation reactions. Given this, we propose the fluorine incorporation strategy to the Pd decorated TiO2, via the sequential doping process, using hydrogen and fluorine exhibiting a record photocurrent of similar to 2 mA cm(-2) (at 1.23 V vs RHE under 1 sun condition), and enhanced rhodamine B degradation. The physicochemical origin of increased photocatalytic activity is ascribed to the effective fluorine doping into the TiO2 lattice via O-vacancies, and to the resulting modified band electronic structure that gen-erates high energy carriers. Furthermore, an insight into the properties of sequential doped Pd loaded TiO2 nanorod (Pd/F:TiO2-x NR), under the scheme of F-Ti3+ gap, states that mediated photocatalysis is provided with Ti-F bonding. Importantly, nanoscale imaging is used to monitor the direct charge at the surface of doped TiO2, which revealed valuable insights for the enhanced photocatalytic activity of TiO2.

Automated summary

Band structure engineering is employed to enhance photocatalytic properties of TiO2 for H-2 production and dye degradation reactions through fluorine doping, resulting in high energy carriers. Nanoscale imaging reveals insights into the enhanced photocatalytic activity of doped TiO2, particularly in the presence of Ti-F bonding in the sequential doped Pd loaded TiO2 nanorod.