Highly Efficient Sunlight‐Driven Photocatalytic Activity of Cu‐Doped BiOBr/g‐C3N4 Nanocomposite via Z‐Scheme Design

Abstract Pharmaceutical pollutants introduce highly intricate compounds into the environment due to extensive structural and functional alterations resulting in adverse health effects on organisms. Herein, a novel nanocomposite is designed comprising Cu‐doped BiOBr nanoflakes and g‐C 3 N 4 to form a dual absorber based on the organic‐inorganic electronic interface for photocatalytic degradation of tetracycline (TC). With incorporating Cu in BiOBr and compositing with g‐C 3 N 4 , the band gap decreased from 2.74 eV to 2.36 eV for BiOBr:Cu/g‐C 3 N 4 , and also light harvesting ability increased. The investigation into the degradation rate considered factors such as pH, TC concentration, photocatalyst dosage, and irradiation time, resulting in a TC degradation efficiency of 98 % within 60 min. In the prepared nanocomposite, photo‐generated electrons of BiOBr can recombine via Cu atoms as a mediator with holes in the valence band of g‐C 3 N 4 due to their band structure position which leads to improved electron/hole separation and enhanced photocatalytic activity. The predominant active species involved in the degradation process were found to be superoxide radicals. Additionally, the photocatalyst exhibited excellent stability, retaining 88 % of its photocatalytic activity after four cycles.