Currently, there is an urgent demand for developing new materials to remove antibiotics in the water environment, especially for the simultaneous degradation of multiple antibiotics. Here, we fabricated a novel Bi/BiOBr heterostructure via an in situ solvothermal strategy, and it exhibited excellent visible-light-responsive photocatalytic activity for synchronously removing multiple antibiotics coexisting in water. The Bi nanoparticles could extend the light absorption spectra of the sample and further facilitate electron-hole pair separation. The in-depth electron spin resonance (ESR) results confirm that the active species in Bi/BiOBr are holes (h+) and superoxide radicals (·O2-) under irradiation, and it is also proved that Bi could selectively reduce the formation of ·O2- in the BiOBr matrix. The coexisting system of TC (tetracycline hydrochloride), CIP (ciprofloxacin) and DOX (doxycycline) could be simultaneously photodegraded to approximately 0% within 30 min by the Bi/BiOBr photocatalyst.
CITATION STYLE
Cao, F., Wang, J., Wang, Y., Zhou, J., Li, S., Qin, G., & Fan, W. (2019). An: In situ Bi-decorated BiOBr photocatalyst for synchronously treating multiple antibiotics in water. Nanoscale Advances, 1(3), 1124–1129. https://doi.org/10.1039/c8na00197a
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