Strategies for enhancing performance of perovskite bismuth ferrite photocatalysts (BiFeO3): A comprehensive review.

Organic pollutants pose a significant threat to water safety, and their degradation is of paramount importance. Photocatalytic technology has emerged as a promising approach for environmental remediation, and Bismuth ferrite (BiFeO3) has been shown to exhibit remarkable potential for photocatalytic degradation of water pollutants, with its excellent crystal structure properties and visible light photocatalytic activity. This review presents an overview of the crystal properties and photocatalytic mechanism of perovskite bismuth ferrite (BiFeO3), as well as a summary of various strategies for enhancing its efficiency in photocatalytic degradation of organic pollutants. These strategies include pure phase preparation, microscopic modulation, composite modification of BiFeO3, and the integration of Fenton-like reactions and external field-assisted methods to improve its photocatalytic performance. The review emphasizes the impact of each strategy on photocatalytic enhancement. By providing comprehensive strategies for improving the efficiency of BiFeO3 photocatalysis, this review inspires new insights for efficient degradation of organic pollutants using BiFeO3 photocatalysis and contributes to the development of photocatalysis in environmental remediation.

Fabrication of novel three-dimensional Fe3O4-based particles electrodes with enhanced electrocatalytic activity for Berberine removal.

Reasonable design of three-dimensional (3D) catalytic particle electrodes (CPEs) is crucial for achieving efficient electrocatalytic oxidation of organic pollutants. Herein, the novel Fe3O4/SnO2/GO (FO/SO/GO) particle electrode has been developed and serviced to the 3D electrocatalytic berberine hydrochloride oxidation system with DSA (RuO2-IrO2-SnO2/Ti) electrode as anode and GDE (gas diffusion electrode) electrode as the cathode. Compared with 2D systems and other CPEs, FO/SO/GO electrode shows excellent electrocatalytic activity and remarkable stability for BH removal, that is, the removal rate of BH is 94.8% within 90 min, and the rate constant is 0.03095 min-1. More importantly, after five cycles, the ternary composite still maintains a strong ability to oxidize pollutants. The structural characterization and electrochemical measurement further uncover that the electron transfer ability and electrocatalytic oxidation efficiency are highly dependent on the surface structure regulation of CPEs. Furthermore, the quenching experiments show that hydroxyl radicals are the main active species in the 3D electro-Fenton (EF) system, which can oxidize BH molecules adsorbed on the surface of GO to CO2, H2O, or other products. The results could potentially provide new insights for designing and fabricating more stable and efficient 3D CPEs electrocatalytic removal of organic pollutants in the future.