摘要

Herein a simple one-step process for preparing a g-C3N4-based green phosphor was presented, which just involved thermal polymerization of a single precursor, 2,4-diamino-6-phenyl-1,3,5-triazine, under an atmosphere of argon, to prepare phenyl-modified g-C3N4. The effects of the annealing temperature and time on the crystalline structure, chemical composition, morphology, optical absorption properties, and photoluminescence emission behavior of the obtained samples were investigated systematically. It was found that the phenyl-modified g-C3N4 prepared at 400 degrees C for 40 min exhibits strong green emission with a quantum yield of as high as 38.08%, comparable to those of the g-C3N4 nanoparticles and quantum dots obtained from the multi-step preparation and post-treatment processes. The emission spectrum of the phenyl-modified g-C3N4 sample can be fitted into four peaks centered at around 465, 490, 520 and 545 nm, suggesting that the phenyl-modified g-C3N4 phosphor possesses multi-fluorophores or luminescent species. The introduction of the phenyl groups leads to the decrease in band gap and thus the red shift in emission as compared with pristine g-C3N4. The simple preparation process along with high quantum yield make this phenyl-modified g-C3N4 green phosphor show great potential in practical applications.