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A Novel CuBi 2 O 4 /BiOBr Direct Z‐scheme Photocatalyst For Efficient Antibiotics Removal: Synergy of Adsorption and Photocatalysis on Degradation Kinetics and Mechanism Insight
Author(s) -
Huang Shushu,
Wang Guodong,
Liu Jiaqi,
Du Chunfang,
Su Yiguo
Publication year - 2020
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.202000634
Subject(s) - photocatalysis , adsorption , kinetics , tetracycline antibiotics , tetracycline , chemical engineering , mineralization (soil science) , chemistry , degradation (telecommunications) , decomposition , catalysis , materials science , photochemistry , organic chemistry , antibiotics , physics , telecommunications , biochemistry , quantum mechanics , computer science , nitrogen , engineering
A novel direct Z‐scheme CuBi 2 O 4 /BiOBr heterostructural photocatalyst was developed aiming to modulate the adsorption ability and photocatalytic degradation performance toward antibiotics. Tetracycline as the model antibiotics was found to show pH value and temperature dependent adsorption capacity over CuBi 2 O 4 /BiOBr. The adsorption process was fitted to Pseudo‐second‐order and Elovich kinetic models and adsorption isotherm was followed Freundich isotherm model. Junction of CuBi 2 O 4 and BiOBr can modulate the surface feature and interfacial interactions, leading to direct Z‐scheme charge kinetics for improved photocatalytic activity. The adsorptive capability and photocatalytic performance of CuBi 2 O 4 /BiOBr heterojunction showed great improvement in comparison with pristine CuBi 2 O 4 and BiOBr. The mineralization process and intermediates for tetracycline degradation were identified by total organic carbon analysis and liquid chromatograph‐tandem mass spectrometry. Plausible transformation pathway and photocatalytic mechanism were proposed. Radical trapping experiments indicated that photogenerated holes and ⋅O 2 − active species played crucial roles in photocatalytic tetracycline decomposition.