Heterojunction of N/B/RGO and g-C3N4 anchored magnetic ZnFe2O4@ZnO for promoting UV/Vis-induced photo-catalysis and in vitro toxicity studies

To promote the low photocatalytic efficiency caused by the recombination of electron/hole pairs and widen the photo-response wavelength window, ZnFe2O4@ZnO-N/B/RGO and ZnFe2O4@ZnO-C3N4 ternary heterojunction nanophotocatalysts were designed and successfully prepared through a sol-gel technique. In comparison to bare ZnFe2O4 and ZnO, the ZnFe2O4-ZnO@N/B/RGO and ZnFe2O4@ZnO-C3N4 ternary products showed highly improved photocatalytic properties in the degradation of methyl orange (MO) under ultra-violet (UV) and visible light irradiation. Various physicochemical properties of the photocatalysts were evaluated through field emission scanning electron microscopy (FESEM), energy-dispersive X-ray (EDX) analysis, X-ray diffraction (XRD), UV-visible diffuse reflectance spectroscopy (DRS), Fourier transform infrared spectroscopy (FT-IR), and vibrating sample magnetometer (VSM) techniques. The observations indicated that the ternary heterojuncted ZnFe2O4@ZnO-N/B/RGO absorbs lower energy visible light wavelengths, which is an enhancement in the photocatalytic properties of ZnFe2O4@ZnO loaded on reduced graphene oxide (RGO) nanosheets and graphite-like carbon nitride (g-C3N4). This gives the catalyst photo-Fenton degradation properties.

Automated summary

In this study, ZnFe2O4@ZnO-N/B/RGO and ZnFe2O4@ZnO-C3N4 ternary heterojunction nanophotocatalysts were successfully prepared via sol-gel technique, demonstrating significantly improved photocatalytic properties compared to bare ZnFe2O4 and ZnO, especially in the degradation of methyl orange under UV and visible light irradiation. The ternary heterojuncted ZnFe2O4@ZnO-N/B/RGO was found to absorb lower energy visible light wavelengths, enhancing the photocatalytic properties of ZnFe2O4@ZnO loaded on reduced graphene oxide (RGO) nanosheets and graphite-like carbon nitride (g-C3N4), providing photo-Fenton degradation properties for the catalyst.