Coupling of Bi2O3 nanoparticles with g-C3N4 for enhanced photocatalytic degradation of methylene blue

Tremendous demands for visible-light-induced catalysts with excellent degradation performance have attracted wide spread attention on designing versatile Bi2O3-based heterojunctions. Herein we designed and synthesized Z-scheme Bi2O3/g-C3N4 heterojunctions using in-situ thermal polymerization method. A tight contact interface between Bi2O3 and g-C3N4 confirmed the formation of heterojunction, facilitating the efficient separation of photo-generated charge carriers. In comparison with pure Bi2O3 and g-C3N4, the 0.5-Bi2O3/g-C3N4 hetemjunctions showed enhanced visible-light-induced catalytic activity which could degrade 100% of methylene blue within 90 min .OH radicals played the most crucial roles and .O-2(-), h(+), e(-) radicals were less contributing in methylene blue photocatalytic elimination. According to the direct evidence of active species capture experiment, PL spectra, HRTEM and well-matched band positions, a Z-scheme enhanced photocatalytic mechanism was put forward. In addition, possible degradation pathways for methylene blue were deduced according to the UPLC-MS results. The present research may provide a way for developing novel Bi2O3-based materials with special application in environmental purification.

Automated summary

The designed Bi2O3/g-C3N4 heterojunction catalyst exhibited excellent degradation performance under visible light, with OH radicals playing a key role and forming a Z-scheme enhanced photocatalytic mechanism.