期刊
CHEMICAL ENGINEERING JOURNAL
卷 455, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.140943
关键词
Metal -organic framework (MOF); S -scheme heterojunction; Cr(VI) removal; MIL-101(Fe); Bi 2 WO 6 microspheres; Antibiotic destruction; Toxicity analysis
Solar-driven elimination of refractory contaminants is an ideal approach for environmental remediation. However, the photocatalytic performance of photocatalysts is limited by insufficient reactive sites and fast recombination of electrons and holes. In this study, a novel metal-organic framework-based heterostructure of MIL-101(Fe)/Bi2WO6 was synthesized, which exhibited significantly enhanced photoactivity for Cr(VI) reduction and tetracycline hydrochloride oxidation compared to individual Bi2WO6 and MIL-101(Fe). The improved catalytic performance can be attributed to the enlarged surface area and pollutant adsorption facilitated by MIL-101(Fe), as well as the efficient photo-carrier transport mechanism supported by oxygen vacancies.
Solar-driven elimination of refractory contaminants is an ideal route to tackle the environmental issues. Nevertheless, the photocatalytic performance of photocatalysts is heavily restrained due to the insufficient accessible reactive sites and fast electrons/holes reunion. Herein, a novel metal-organic framework-based S -scheme heterostructure of MIL-101(Fe)/Bi2WO6 was synthesized by a simple solvothermal approach. The opti-mized MIL-101(Fe)/Bi2WO6 (MIL/BWO-2) affords the highest photo-activities under visible light, which are 13.7, 6.7 folds greater for Cr(VI) reduction, and 0.8, 10.5 folds higher for tetracycline hydrochloride oxidation compared with individual Bi2WO6 and MIL-101(Fe), respectively. The preeminent catalytic capability lies in two aspects: 1) the introduction of MIL-101(Fe) substantially enlarges the surface area of the composites, offering ample reaction sites and fostering pollutant adsorption and mass transportation; 2) the novel S-scheme photo -carrier transport mechanism assisted by oxygen vacancies favors spatial segregation and transport of photoin-duced electrons/holes with superior redox capacity. Reactive species identification experiments verify that center dot O2- and e- dominantly contribute to Cr(VI) reduction, while center dot O2-, h+ and center dot OH account for tetracycline hydrochloride destruction. Furthermore, the tetracycline photo-decomposition pathway, eco-toxicity evaluation, and photo -catalytic mechanism were investigated comprehensively. This research paves the way for building high-performance MOFs-based S-scheme heterojunctions toward photocatalytic water purification.
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