Gas-Phase Fluorination of g-C3N4 for Enhanced Photocatalytic Hydrogen Evolution

Graphitic carbon nitride (g-C3N4) has attracted much attention because of its potential for application in solar energy conservation. However, the photocatalytic activity of g-C3N4 is limited by the rapidly photogenerated carrier recombination and insufficient solar adsorption. Herein, fluorinated g-C3N4 (F-g-CN) nanosheets are synthesized through the reaction with F-2/N-2 mixed gas directly. The structural characterizations and theoretical calculations reveal that fluorination introduces N vacancy defects, structural distortion and covalent C-F bonds in the interstitial space simultaneously, which lead to mesopore formation, vacancy generation and electronic structure modification. Therefore, the photocatalytic activity of F-g-CN for H-2 evolution under visible irradiation is 11.6 times higher than that of pristine g-C3N4 because of the enlarged specific area, enhanced light harvesting and accelerated photogenerated charge separation after fluorination. These results show that direct treatment with F-2 gas is a feasible and promising strategy for modulating the texture and configuration of g-C3N4-based semiconductors to drastically enhance the photocatalytic H-2 evolution process.

Automated summary

Fluorinated g-C3N4 nanosheets were synthesized through reaction with F-2 gas, resulting in increased specific area, enhanced light absorption and accelerated charge separation, leading to improved photocatalytic hydrogen evolution activity.