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Facile construction of Z-scheme Fe-MOF@BiOBr/M−CN heterojunction for efficient degradation of ciprofloxacin

[Display omitted] •A novel Fe-MOF@BiOBr/M−CN ternary system was successfully synthetized by one-pot.•Fe-MOF@BiOBr/M−CN facilitated e--h+ separation and enhanced degradation process.•The products of CIP photocatalytic degradation were environmentally friendly.•Plausible photodegradation pathway of CI...

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Published in:Separation and purification technology 2022-08, Vol.295, p.121216, Article 121216
Main Authors: Pan, Yaping, Hu, Xin, Shen, Dongcai, Li, Zhe, Chen, Rong, Li, Yiming, Lu, Jinren, Bao, Mutai
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Hu, Xin
Shen, Dongcai
Li, Zhe
Chen, Rong
Li, Yiming
Lu, Jinren
Bao, Mutai
description [Display omitted] •A novel Fe-MOF@BiOBr/M−CN ternary system was successfully synthetized by one-pot.•Fe-MOF@BiOBr/M−CN facilitated e--h+ separation and enhanced degradation process.•The products of CIP photocatalytic degradation were environmentally friendly.•Plausible photodegradation pathway of CIP was illustrated based on GC–MS.•A possible Z-type heterojunction was formed between M−CN and BiOBr. A novel Fe-MOF@BiOBr/M−CN photocatalyst is synthesized via one-pot EG (ethylene glyco)-assisted solvothermal heating. The morphology, microstructure, and composition of the prepared catalysts are characterized by SEM, XRD, FTIR, and XPS. The Fe-MOF@BiOBr/M−CN photocatalyst exhibites better pollutant adsorption and degradation than pure BiOBr. After grafting iron-based metal–organic framework (Fe-MOF) and modified g-C3N4 (M−CN) species, photogenerated electrons can be transferred from BiOBr to M−CN and Fe-MOF species via interfacial charge transfer. Therefore, the separation efficiency of electrons (e−) and holes (h+) is enhanced. Fe-MOF@BiOBr/M−CN−50 can degrade approximately 93% of ciprofloxacin in 120 min under visible light illumination, which is 7.9 and 1.2 times that of pure g-C3N4 (11.8%) and BiOBr (77.4%), respectively. Furthermore, radical capturing experiments and ESR analysis reveal that h+ and ·O2− are the main reactive species in the system. A combination of DFT calculations and radical trapping experiments show that M−CN and BiOBr form a Z-type heterojunction. In addition, Fe-MOF plays a vital role as a carrier acceptor for electron transport. Finally, the degradation pathway of ciprofloxacin is revealed by gas-chromatography–mass-spectroscopy analysis. This study provides new insights into the photocatalytic degradation of pollutants in water.
doi_str_mv 10.1016/j.seppur.2022.121216
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A novel Fe-MOF@BiOBr/M−CN photocatalyst is synthesized via one-pot EG (ethylene glyco)-assisted solvothermal heating. The morphology, microstructure, and composition of the prepared catalysts are characterized by SEM, XRD, FTIR, and XPS. The Fe-MOF@BiOBr/M−CN photocatalyst exhibites better pollutant adsorption and degradation than pure BiOBr. After grafting iron-based metal–organic framework (Fe-MOF) and modified g-C3N4 (M−CN) species, photogenerated electrons can be transferred from BiOBr to M−CN and Fe-MOF species via interfacial charge transfer. Therefore, the separation efficiency of electrons (e−) and holes (h+) is enhanced. Fe-MOF@BiOBr/M−CN−50 can degrade approximately 93% of ciprofloxacin in 120 min under visible light illumination, which is 7.9 and 1.2 times that of pure g-C3N4 (11.8%) and BiOBr (77.4%), respectively. Furthermore, radical capturing experiments and ESR analysis reveal that h+ and ·O2− are the main reactive species in the system. A combination of DFT calculations and radical trapping experiments show that M−CN and BiOBr form a Z-type heterojunction. In addition, Fe-MOF plays a vital role as a carrier acceptor for electron transport. Finally, the degradation pathway of ciprofloxacin is revealed by gas-chromatography–mass-spectroscopy analysis. 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A novel Fe-MOF@BiOBr/M−CN photocatalyst is synthesized via one-pot EG (ethylene glyco)-assisted solvothermal heating. The morphology, microstructure, and composition of the prepared catalysts are characterized by SEM, XRD, FTIR, and XPS. The Fe-MOF@BiOBr/M−CN photocatalyst exhibites better pollutant adsorption and degradation than pure BiOBr. After grafting iron-based metal–organic framework (Fe-MOF) and modified g-C3N4 (M−CN) species, photogenerated electrons can be transferred from BiOBr to M−CN and Fe-MOF species via interfacial charge transfer. Therefore, the separation efficiency of electrons (e−) and holes (h+) is enhanced. Fe-MOF@BiOBr/M−CN−50 can degrade approximately 93% of ciprofloxacin in 120 min under visible light illumination, which is 7.9 and 1.2 times that of pure g-C3N4 (11.8%) and BiOBr (77.4%), respectively. Furthermore, radical capturing experiments and ESR analysis reveal that h+ and ·O2− are the main reactive species in the system. A combination of DFT calculations and radical trapping experiments show that M−CN and BiOBr form a Z-type heterojunction. In addition, Fe-MOF plays a vital role as a carrier acceptor for electron transport. Finally, the degradation pathway of ciprofloxacin is revealed by gas-chromatography–mass-spectroscopy analysis. 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A novel Fe-MOF@BiOBr/M−CN photocatalyst is synthesized via one-pot EG (ethylene glyco)-assisted solvothermal heating. The morphology, microstructure, and composition of the prepared catalysts are characterized by SEM, XRD, FTIR, and XPS. The Fe-MOF@BiOBr/M−CN photocatalyst exhibites better pollutant adsorption and degradation than pure BiOBr. After grafting iron-based metal–organic framework (Fe-MOF) and modified g-C3N4 (M−CN) species, photogenerated electrons can be transferred from BiOBr to M−CN and Fe-MOF species via interfacial charge transfer. Therefore, the separation efficiency of electrons (e−) and holes (h+) is enhanced. Fe-MOF@BiOBr/M−CN−50 can degrade approximately 93% of ciprofloxacin in 120 min under visible light illumination, which is 7.9 and 1.2 times that of pure g-C3N4 (11.8%) and BiOBr (77.4%), respectively. Furthermore, radical capturing experiments and ESR analysis reveal that h+ and ·O2− are the main reactive species in the system. A combination of DFT calculations and radical trapping experiments show that M−CN and BiOBr form a Z-type heterojunction. In addition, Fe-MOF plays a vital role as a carrier acceptor for electron transport. Finally, the degradation pathway of ciprofloxacin is revealed by gas-chromatography–mass-spectroscopy analysis. This study provides new insights into the photocatalytic degradation of pollutants in water.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.seppur.2022.121216</doi></addata></record>
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subjects BiOBr
Ciprofloxacin
Graphitic Carbon Nitrides
MIL-Fe
Photocatalytic degradation
title Facile construction of Z-scheme Fe-MOF@BiOBr/M−CN heterojunction for efficient degradation of ciprofloxacin
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