Influence of Nonmetal Dopants on Charge Separation of Graphitic Carbon Nitride by Time-Dependent Density Functional Theory

Abstract

Photocatalysts are crucial materials for green energy production and environmental purification. Non-metal doped graphitic carbon nitride (g-C3N4) has attracted much attention in recent years because of low-cost and desired photocatalytic performance characteristics such as high charge separation efficiency and broad visible light absorption. In this study, we used time-dependent density functional theory and wave function analysis to evaluate the charge separation characteristics of phosphorus-, oxygen- and sulfur-doped g-C3N4 upon photon excitation based on electron-hole pair distances, electron-hole pair overlaps, and charge transfer amounts. The lowest unoccupied molecular orbital of doped heptazine rings was shifted downward to facilitate electron transfer from undoped to doped heptazine rings upon photon excitation. Generally, the phosphorus dopant yielded relatively high charge transfer, high electron-hole pair separations, and low electron-hole overlap compared with the oxygen and sulfur dopants. In a low concentration, the sulfur dopant had the similar performance as the phosphorus dopant did. Furthermore, the phosphorus dopant attracted photon excited electrons, whereas the oxygen and sulfur dopants contributed to electron-hole pair separation. The dopants concentrated in one heptazine ring exhibited high charge separation performance than those dopants distributed among multiple heptazine rings in g-C3N4; the simulation results suggested that doping configurations are more crucial than doping concentrations with respect to charge separation efficiency in nonmetal-doped g-C3N4.