Self-assembled synthesis of oxygen-doped g-C3N4 nanotubes in enhancement of visible-light photocatalytic hydrogen

Currently, photocatalytic water splitting is regarded as promising technology in renewable energy generation. However, the conversion efficiency suffers great restriction due to the rapid recombination of charge carriers. Rational designed the structure and doping elements become important alternative routes to improve the performance of photocatalyst. In this work, we rational designed oxygen-doped graphitic carbon nitride (OCN) nanotubes derived from supermolecular intermediates for photocatalytic water splitting. The as prepared OCN nanotubes exhibit an outstanding hydrogen evolution rate of 73.84 mu mol h(-1), outperforming the most of reported one dimensional (1D) g-C3N4 previously. Due to the rational oxygen doping, the band structure of g-C3N4 is meliorated, which can narrow the band gap and reduce the recombination rate of photogenerated carriers. Furthermore, the hollow nanotube structure of OCN also provide multiple diffuse reflection during photocatalytic reaction, which can significantly promote the utilization capacity of visible light and enhance the photocatalytic water splitting performance. It is believed that our work not only rationally controls the nanostructure, but also introduces useful heteroatom into the matrix of photocatalyst, which provides an effective way to design high-efficiency g-C3N4 photocatalyst. (C) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

Automated summary

By rational oxygen doping, the band structure of g-C3N4 is improved, narrowing the band gap and reducing the recombination rate of photogenerated carriers. Additionally, the hollow nanotube structure of OCN provides multiple diffuse reflection during photocatalytic reaction, significantly enhancing the utilization capacity of visible light and improving the photocatalytic water splitting performance.