Abstract

A novel BiOBr photocatalyst was epitaxially grown in situ onto the surface of ZnFe2O4, a ferroelectric material with a strong polarization effect. The formatted BiOBr/ZnFe2O4 composite (BOB/ZFO) showed excellent photocatalytic degradation performance of tetracycline antibiotics (TCs). One of the composites with ZnFe2O4 content of 10% (BOB/ZFO-10) showed the best properties; the degradation efficiency of TCs upon visible light irradiation for 180 min was 99.2%, which was 3.58 times higher than that of pure phase BiOBr. The functions of ZnFe2O4 are assumed to be such that the addition of this ferroeletric material not only regulated the spontaneous polarization of BiOBr in the process of synthesis, but also resulted in the construction of Z-scheme heterostructures due to the appropriate staggered band structure of BiOBr and ZnFe2O4. In the presence of ferroelectric material ZnFe2O4, the local structure of BiOBr may be distorted accordingly, resulting in preferential growth of a (110) crystal facet of BiOBr and enhancement of spontaneous polarization, which promotes the efficient separation of photogenerated electron-hole pairs of ZnFe2O4 and BiOBr, and therefore enhances the redox capacity of the photocatalytic degradation of organic pollutants.

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