Construction of direct Z-scheme Bi5O7I/UiO-66-NH2 heterojunction photocatalysts for enhanced degradation of ciprofloxacin: Mechanism insight, pathway analysis and toxicity evaluation.

Abstract

Direct Z-scheme Bi₅O₇I/UiO-66-NH₂ (denoted as BU-x) heterojunction photocatalysts were successfully constructed through ball-milling method. Photocatalytic activities of the as-prepared BU-x samples were determined by using a typical fluoroquinolone antibiotic, ciprofloxacin (CIP). All BU-x heterojunctions exhibited better CIP removal performances than that of pristine Bi₅O₇I and UiO-66-NH₂ upon exposure to white light irradiation. In comparison, the heterojunction with UiO-66-NH₂ content of 50 wt% (BU-5) showed excellent structural stability and the optimal adsorption-photodegradation efficiency for the CIP removal. The removal efficiency of CIP (10 mg/L) over BU-5 (0.75 g/L) achieved 96.1% within 120 min illumination. Meanwhile, the effect of photocatalyst dosage, pH and inorganic anions were systemically explored. Reactive species trapping experiments, electron spin resonance (ESR) signals, Mott-Schottky measurements and density functional theory (DFT) simulation revealed that the photo-generated holes (h⁺), hydroxyl radical (·OH) and superoxide radical (·O₂^-) played crucial roles in CIP degradation. This result can be ascribed to that the unique Z-scheme charge transfer configuration retained the excellent redox capacities of Bi₅O₇I and UiO-66-NH₂. Meanwhile, the CIP degradation pathways and the toxicity of various intermediates were subsequently analyzed. This work provided a feasible idea for removing antibiotics by bismuth-rich bismuth oxyhalide/MOF-based heterostructured photocatalysts.