A serious threat to human health and the environment worldwide, in addition to the global energy crisis, is the increasing water pollution caused by micropollutants such as antibiotics and persistent organic dyes. Nanostructured semiconductors in advanced oxidation processes using photocatalysis have recently attracted a lot of interest as a promising green and sustainable wastewater treatment method for a cleaner environment. Due to their narrow bandgaps, distinctive layered structures, plasmonic, piezoelectric and ferroelectric properties, and desirable physicochemical features, bismuth-based nanostructure photocatalysts have emerged as one of the most prominent study topics compared to the commonly used semiconductors (TiO2 and ZnO). In this review, the most recent developments in the use of photocatalysts based on bismuth (e.g., BiFeO3, Bi2MoO6, BiVO4, Bi2WO6, Bi2S3) to remove dyes and antibiotics from wastewater are thoroughly covered. The creation of Z-schemes, Schottky junctions, and heterojunctions, as well as morphological modifications, doping, and other processes are highlighted regarding the fabrication of bismuth-based photocatalysts with improved photocatalytic capabilities. A discussion of general photocatalytic mechanisms is included, along with potential antibiotic and dye degradation pathways in wastewater. Finally, areas that require additional study and attention regarding the usage of photocatalysts based on bismuth for removing pharmaceuticals and textile dyes from wastewater, particularly for real-world applications, are addressed.
Conventional methods are inefficient to treat water contaminated with persistent organic contaminants. To decontaminate bacteria and 2,4,5‐trichlorophenol (TCP) contaminated water, a heterogeneous photocatalysis‐based advanced oxidation process was applied in this study. A Li‐doped ternary Zn0.5Ni0.5Fe2O4 (ZNF) photocatalyst (Li/ZNF) was synthesized via a facile co‐precipitation technique and characterized. The Li/ZNF has a sufficient specific surface area (69.8 m2.g−1), and an appropriate bandgap of 2.89 eV. Under optimal conditions, 10 mg of Li/ZNF photocatalyst degraded 80 % of 50 mg L−1 TCP in 6 h at pH 3 in the presence of 4 mM H2O2. After use, the Li/ZNF photocatalyst was magnetically separated and reused numerous times, with an efficiency of 66 % after the fifth reuse cycle. In the antibacterial time‐kill assay, 15 and 25 mg of Li/ZNF inhibited 1×107 CFU.mL−1 of S. Aureus and E. coli bacteria after 60 min of UV exposure, respectively.
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