期刊
JOURNAL OF ALLOYS AND COMPOUNDS
卷 854, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2020.157166
关键词
BiOI; MOF; Photocatalyst; Tetracycline degradation
资金
- National Natural Science Foundation of China [21576112, 21902060]
- Natural Science Foundation Project of Jilin Province [20180623042TC, 20180101181JC, 20170520147JH]
- Project of Human Resources and Social Security Department of Jilin Province [2017956]
- Project of Development and Reform Commission of Jilin Province [2019C044-2]
- Project of Education Department of Jilin Province [JJKH20191009KJ, JJKH20191015KJ]
A series of BiOI/MIL-125(Ti) composites were prepared by coupling semiconductor with metal-organic framework via one-step hydrothermal method. The optimized composite showed excellent photocatalytic activity with 80% degradation efficiency for tetracycline and superior stability and reusability in successive catalytic runs. The enhanced photocatalytic activity was attributed to high specific surface area, promoting visible light absorption, and efficient charge transfer of the composites.
Herein, coupling semiconductor with metal-organic framework, a series of BiOI/MIL-125(Ti) composites have been prepared via one-step hydrothermal method. Morphology analyses reveal that the formation of heterostructure and the BiOI is uniformly covering on the surface of MIL-125(Ti). Under visible light illumination, the optimized 9 wt% BiOI/MIL-125(Ti) composite (BT-9) exhibits excellent photocatalytic activity for the degradation of tetracycline (TC) and the efficiency could reach 80%, which is much higher than that of bare BiOI and MIL-125(Ti). In particular, the BT-9 photocatalyst features superior stability and reusability in successive catalytic runs. Based on the comprehensive characterization studies, the enhancement of photocatalytic activity can be ascribed to the high specific surface area, promoting visible light absorption and outstanding efficiency of charge transfer of BiOI/MIL-125(Ti) composites. (C) 2020 Elsevier B.V. All rights reserved.
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