In situ fabrication of the Bi2O3–V2O5 hybrid embedded with graphitic carbon nitride nanosheets: Oxygen vacancies mediated enhanced visible-light–driven photocatalytic degradation of organic pollutants and hydrogen evolution

Novel mesoporous ternary hybrids comprising Bi2O3/V2O5 photocatalysts anchored on graphitic carbon nitride (g-C3N4) nanosheets were synthesized via an in situ co-pyrolysis approach and characterized by a series of techniques, including X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy (TEM), high-resolution TEM, X-ray photoelectron spectroscopy, Brunauer–Emmett–Teller analysis, thermogravimetric-differential thermal analysis, Fourier transform infrared spectroscopy, ultraviolet–visible spectrometry, photoluminescence and electron paramagnetic resonance (EPR). The hybrids were subsequently tested as photocatalysts for the degradation of the phenol red (PR) pollutant under visible light irradiation. The well-designed ternary hybrids showed pure and randomly distributed Bi2O3/V2O5 (denoted as BiV) nanoparticles on monodispersed g-C3N4 nanosheets. The as-prepared ternary Bi2O3/V2O5@g-C3N4 (i.e., [email protected]3N4) hybrids demonstrated high specific surface areas with remarkable mesoporous characteristics. The photodegradation efficiencies of the ternary hybrids for PR were 1.2 and 1.8 times higher than those of binary BiV and pristine Bi2O3, respectively, at 50 min irradiation time under simulated solar light irradiation. At the end of the phototreatment, the amount of PR pollutant was reduced to 98.1% in 50 min by using the [email protected]3N4 nanocomposites under simulated solar light irradiation and more efficient for photocatalytic H2 production. Based on an electrochemical analysis, we propose a photocatalytic degradation pathway for PR under visible light irradiation. In addition, the [email protected]3N4 nanocomposite photocatalysts exhibited both long-term stability and photocatalytic efficiency for the degradation of the PR dye. The excellent photoelectrochemical performance of the [email protected]3N4 photocatalysts can be ascribed to their highly dispersed V2O5 and Bi2O3 nanoparticles, mesoporous structure, and high specific surface area (83.75 m2 g−1).