Abstract
The search for stable, high-performance, and low-cost photocatalysts has received considerable interest. In this work, mesoporous LaVO4 nanoparticles were synthesized for the first time by applying the soft template, and g-C3N4 nanosheets were fabricated using a hard template to design mesoporous LaVO4/g-C3N4 heterostructures. The synthesized photocatalysts were assessed by the mineralization of trichloroethylene (TCE) in aqueous media during visible illumination. TEM and XRD measurements verified the existence of porous g-C3N4 with a high distribution of the monoclinic phase LaVO4 NPs (5 nm). The photocatalytic performance of the LaVO4/g-C3N4 heterojunction was much better than that of either LaVO4 or g-C3N4. 3%LaVO4/g-C3N4 exhibited the maximum photocatalytic ability, about 99% during a 3 h illumination at a degradation rate of 6.50 mu molL(-1) min(-1), which were -3.89-and-4.67-fold greater than parent LaVO4 and g-C3N4, respectively. The first-order kinetics calculations revealed that the 3% LaVO4/g-C3N4 heterostructure offered the highest rate constant of 0.0113 min(-1), which estimated-8.7 and 4.9 folds larger than LaVO4 (0.0023 min(-1)) and g-C3N4 (0.0015 min(-1)), respectively. The importance of the LaVO4/g-C3N4 with superb photocatalytic efficiency was demonstrated based on the photoluminescence spectra, transient photocurrent curves, and UV-visible absorption spectra. The obtained LaVO4/g-C3N4 photocatalyst exhibited excellent regeneration and recyclability over five consecutive runs. The coupling of LaVO4 and g-C3N4 with matching alignment potentials and the synergetic effect were thought to be the most interesting processes to promote photocatalytic efficiency. The obtained LaVO4/g-C3N4 heterojunction possesses excellent photocatalytic efficiency and is a favorable candidate for potential applications in wastewater remediation using solar energy.