Abstract
In this work, oxygen-doped g-C3N4 mesoporous nanosheets (O-CNS) were synthesized via a facile recrystallization method with the assistance of H2O2. The crystal phase, chemical composition, morphological structure, optical property, electronic structure and electrochemical property of the prepared O-CNS samples were well investigated. The morphological observation combined with the nitrogen adsorption-desorption results demonstrated that the prepared O-CNS samples possessed nanosheet-like morphology with a porous structure. Doping O into g-C3N4 resulted in the augmentation of the specific surface area, which could provide more active sites for photocatalytic reactions. Simultaneously, the visible light absorption capacity of O-CNS samples was boosted owing to the regulation of O doping. The built energy level induced by the O doping could accelerate the migration rate of photoinduced carriers, and the porous structure was most likely to speed up the release of hydrogen during the photocatalytic hydrogen process. Resultantly, the photocatalytic hydrogen production rate of the optimized oxygen-doped g-C3N4 nanosheets reached up to 2012.9 μmol·h-1·g-1, which was 13.4 times higher than that of bulk g-C3N4. Thus, the significantly improved photocatalytic behavior was imputed to the synergistic effect of the porous structure, the increase in active sites, and the enhancement of visible light absorption and charge separation efficiency. Our research highlights that the synergistic effect caused by element doping will make a great contribution to the remarkable improvement in photocatalytic activity, providing a new inspiration for the construction of novel catalysts.