Degradation of Organic Dyes by the UCNP/h-BN/TiO₂ Ternary Photocatalyst

Abstract

In this study, upconversion nanoparticles (UCNPs) with a flower-like morphology were prepared using a urea coprecipitation method. A ternary photocatalyst was first prepared using a solvothermal method involving the use of titanium oxide (TiO 2 ), hexagonal boron nitride (h-BN), and UCNPs (Y 2 O 3 , Yb 3+ , and Tm 3+ ) as raw materials. The surface morphology, crystal structure, and functional groups of these materials were then characterized and analyzed through scanning electron microscopy, transmission electron microscopy, X-ray diffraction analysis, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, ultraviolet–visible spectrophotometry, and other techniques. Photocatalytic experiments were also conducted to investigate the effects of different catalyst types, raw material doping ratios, pH values, and catalyst quantities on the photocatalytic degradation of rhodamine B (RhB). The results indicated that doping with h-BN and UCNPs reduced the band gap width of RhB, increased its light absorption rate, and decreased the recombination rate of its photogenerated electrons and holes so that the photocatalytic degradation effect reached 100% within 2 h. After five experimental cycles, the 30% UC-BN-Ti photocatalyst remained highly durable and stable. To investigate the effects of different trapping agents on the degradation of RhB, benzoquinone, isopropanol, and ethylenediaminetetraacetic acid disodium salt were used as free-radical-capturing agents. The results indicated that • O 2– was the primary active species in the degradation process. Finally, the pathway and mechanism of the degradation of RhB through ternary composite photocatalysis were identified.