Switching Oxygen Reduction Pathway by Exfoliating Graphitic Carbon Nitride for Enhanced Photocatalytic Phenol Degradation

The selectivity of molecular oxygen activation on the exfoliated graphitic carbon nitride (g-C3N4) and its influence on the photocatalytic phenol degradation process were demonstrated. Compared with bulk g-C3N4, the exfoliated nanosheet yielded a 3-fold enhancement in photocatalytic phenol degradation. ROS trapping experiments demonstrated that although the direct hole oxidation was mainly responsible for phenol photoclegradation on both g-C3N4 catalysts, molecular oxygen activation processes on their surface greatly influenced the whole phenol degradation efficiency. Reactive oxygen species and Raman spectroscopy measurements revealed that oxygen was preferentially reduced to center dot O-2(-) by one electron transfer on bulk g-C3N4, while on g-C3N4 nanosheet the production of H2O2 via a two electron transfer process was favored due to the rapid formation of surface stabilized 1,4-endoperoxide. The latter process not only promotes the separation of photogenerated electron-hole pairs but also greatly facilitates reactive oxygen species formation and subsequently enhances phenol degradation.