Abstract

Introducing oxygen vacancies and Ti3+ into TiO2 is thought to be an effective method of increasing the utilization of sunlight and promoting the efficiency of electron transfer. In this work, novel carbon and nitrogen self-doped TiO2 hollow spheres (CNTH) with oxygen vacancies and Ti3+ were synthesized by a one-pot hydrothermal strategy in H2OC2H5OHHFH2O2 mixed solution with TiCN as a precursor of anatase TiO2 and self-doping source of N and C. The presence of oxygen vacancies and Ti3+ in the resulting CNTH photocatalyst was supported by electron paramagnetic resonance (EPR) and X-ray absorption near-edge structure spectroscopy (XANES). X-ray photoelectron spectroscopy (XPS) analysis showed that the C and N atoms were successfully self-doped into TiO2 lattice, which resulted in the CNTH materials exhibiting the enhanced absorption in the UV–visible region with a clear red shift at the absorption edges. The electronic structure of CNTH was examined by first-principle density functional theory (DFT) calculations, which further confirmed the optical properties of CNTH for the enhanced visible-light absorption properties and the red-shift phenomenon of the absorption edges. The resulting CNTH photocatalyst showed enhanced visible-light photocatalytic activity for H2 production. The enhanced activity of CNTH was due to the introduction of C and N self-doping and the existence of oxygen vacancies and Ti3+. The former can promote the photocatalytic reactions of the photogeneration electrons and holes on CNTH under visible-light irradiation, while the latter create more active sites and prolong the life time of electrons and holes by their donor states.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call