Synthesis of Z-type spherical B-g-C3N4/Bi2WO6 heterojunctions for enhanced rhodamine B degradation

A spherical B-g-C3N4/Bi2WO6 heterojunction photocatalyst was synthesized using the hydrothermal coprecipi-tation method. Scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), and ultraviolet-visible diffuse reflectance spectroscopy (DRS) showed that B-g-C3N4 was uniformly dispersed on the Bi2WO6 surface through a strong chemical bond, reducing the energy bandgap of Bi2WO6. The outcomes of the experiment regarding the photocatalytic degradation of rhodamine B (RhB) demonstrated a notable enhancement in the degradation rate for the 1:3 BCN/BWO com-posite. Specifically, the degradation rate was found to be 76 times greater than that of B-g-C3N4 and 7 times higher than that of Bi2WO6. Furthermore, a photocatalytic degradation mechanism was proposed based on the results of ultraviolet photoelectron spectroscopy (UPS) and free radical capture experiments. The direct Z-type B-g-C3N4/Bi2WO6 heterojunction structure promotes the effective separation of photogenerated carriers and en-hances their oxidation-reduction ability.

Automated summary

A spherical B-g-C3N4/Bi2WO6 heterojunction photocatalyst was synthesized using the hydrothermal coprecipitation method. The study found that B-g-C3N4 was uniformly dispersed on the Bi2WO6 surface, reducing its energy bandgap. The photocatalytic degradation of rhodamine B showed a significant enhancement in the degradation rate for the 1:3 BCN/BWO composite, with a degradation rate 76 times higher than B-g-C3N4 and 7 times higher than Bi2WO6. The proposed photocatalytic degradation mechanism is based on the results of UPS and free radical capture experiments, and the direct Z-type B-g-C3N4/Bi2WO6 heterojunction structure promotes effective carrier separation and oxidation-reduction ability.