The uniform pore size distribution and inherent particle inseparability of iron-based metal-organic frameworks(Fe-MOFs)have been shown to significantly hinder their light-harvesting capabilities and charge carrier sep...The uniform pore size distribution and inherent particle inseparability of iron-based metal-organic frameworks(Fe-MOFs)have been shown to significantly hinder their light-harvesting capabilities and charge carrier separation efficiency.These intrinsic limitations compromise catalyst recyclability and reaction kinetics in practical scenarios,thereby impeding their applicability in the degradation of antibiotic pollutants such as levofloxacin(LEV)in aquatic environments.Here,we report an S-type heterojunction photocatalyst,MnFe2O4@MIL-101(Fe),prepared via hydrothermal coupling of magnetic MnFe2O4 nanoparticles with MIL-101(Fe).The synergistic effect of Fe3+/Fe2+and Mn3+/Mn2+redox pairs,combined with the heterojunction interface and built-in electric field,significantly enhances visible-light-driven photo-Fenton activity.The catalyst degraded over 95%of LEV with a rate constant of 0.05056 min-1 and retained 87%activity after five cycles.LC-MS analysis revealed defluorination and demethylation pathways,while toxicity assessments confirmed lower LC50,mutagenicity,and developmental toxicity of intermediates,validating the environmental viability of the photo-Fenton process.展开更多
Bi/Bi2Fe4O9nanocomposites consisting of Bi2Fe4O9nanosheets decorated with Bi nanodots were synthesized by a hydrothermal method.The formation of Bi nanodots on the Bi2Fe4O9nanosheet surfaces...Bi/Bi2Fe4O9nanocomposites consisting of Bi2Fe4O9nanosheets decorated with Bi nanodots were synthesized by a hydrothermal method.The formation of Bi nanodots on the Bi2Fe4O9nanosheet surfaces was attributed to the reducibility of 2-methoxyethanol in the precursor solution.Comparative photocatalytic evaluation reveals that the Bi/Bi2Fe4O9nanocomposites significantly enhance the degradation efficiency(99.0%)of bisphenol A compared with Bi2Fe4O9nanosheets(64.2%)under 120 min simulated solar irradiation.This remarkable enhancement can be attributed to the established Bi/Bi2Fe4O9heterojunction structure,which effectively facilitates the separation of photogenerated electron-hole pairs and accelerates interfacial charge transfer between the metallic Bi nanodots and semiconductor Bi2Fe4O9nanosheets.The synergistic effects arising from this unique architecture ultimately lead to superior photocatalytic performance.展开更多
基金supported by the National Natural Science Foundation of China(No.22178325)the Research Fund of Key Laboratory of the Ministry of Education for Advanced Catalysis Materials,Zhejiang Key Laboratory of Advanced Catalysis and Adsorption Materials。
摘要The uniform pore size distribution and inherent particle inseparability of iron-based metal-organic frameworks(Fe-MOFs)have been shown to significantly hinder their light-harvesting capabilities and charge carrier separation efficiency.These intrinsic limitations compromise catalyst recyclability and reaction kinetics in practical scenarios,thereby impeding their applicability in the degradation of antibiotic pollutants such as levofloxacin(LEV)in aquatic environments.Here,we report an S-type heterojunction photocatalyst,MnFe2O4@MIL-101(Fe),prepared via hydrothermal coupling of magnetic MnFe2O4 nanoparticles with MIL-101(Fe).The synergistic effect of Fe3+/Fe2+and Mn3+/Mn2+redox pairs,combined with the heterojunction interface and built-in electric field,significantly enhances visible-light-driven photo-Fenton activity.The catalyst degraded over 95%of LEV with a rate constant of 0.05056 min-1 and retained 87%activity after five cycles.LC-MS analysis revealed defluorination and demethylation pathways,while toxicity assessments confirmed lower LC50,mutagenicity,and developmental toxicity of intermediates,validating the environmental viability of the photo-Fenton process.
基金Funded by the National Natural Science Foundation of China(No.50902108)。
摘要Bi/Bi2Fe4O9nanocomposites consisting of Bi2Fe4O9nanosheets decorated with Bi nanodots were synthesized by a hydrothermal method.The formation of Bi nanodots on the Bi2Fe4O9nanosheet surfaces was attributed to the reducibility of 2-methoxyethanol in the precursor solution.Comparative photocatalytic evaluation reveals that the Bi/Bi2Fe4O9nanocomposites significantly enhance the degradation efficiency(99.0%)of bisphenol A compared with Bi2Fe4O9nanosheets(64.2%)under 120 min simulated solar irradiation.This remarkable enhancement can be attributed to the established Bi/Bi2Fe4O9heterojunction structure,which effectively facilitates the separation of photogenerated electron-hole pairs and accelerates interfacial charge transfer between the metallic Bi nanodots and semiconductor Bi2Fe4O9nanosheets.The synergistic effects arising from this unique architecture ultimately lead to superior photocatalytic performance.