Insight into the Effect of the Cl 3p Orbital on g-C3N4 Mimicking Photosynthesis under CO2 Reduction

Achieving high-efficiency photocatalytic materials to convert CO2 into high-value chemicals is still challenging. Herein, chlorine-doped g-C3N4 photocatalysts (Cl-CN) were successfully synthesized by a simple multiple calcination method. The as-prepared Cl-CN exhibited satisfactory photocatalytic activity in photoreduction of CO2. The CO yield of Cl-CN was about 39.89 mu mol/g. The DRS, UPS, and VB-XPS results indicated a narrower band gap, and the negatively shifted CB potential enhanced the CO2 reduction ability. DFT calculations and the partial density of states revealed that the Cl 3p orbital greatly contributed to the CBM and VBM of Cl-CN, which caused the narrower band gap 1 and an upshift of the conduction band by 0.14 eV over that of bulk-CN. The CO2 conversion intermediate was investigated by in situ Fourier transform infrared spectroscopy, and the corresponding reaction mechanism was proposed according to the density functional theory calculations and experimental results, which showed that Cl doping and the C-Cl bond increased the photogenerated carrier lifetime and the CO2 adsorption capacity of Cl-CN. Therefore, this work provides a deeper understanding of the effect of Cl doping on the g-C3N4 electronic structure and its CO2 reduction activity.

Automated summary

This research successfully synthesized chlorine-doped g-C3N4 photocatalysts (Cl-CN) through a simple multiple calcination method, which exhibited satisfactory photocatalytic activity in the photoreduction of CO2 and provided a deeper understanding of the effect of chlorine doping on the electronic structure and CO2 reduction activity.