1D CuBi2O4@2D UiO-66-NH2 Core-Shell Nanostructures for Photodegradation of Tetracycline Hydrochloride

被引:6
作者
Zhang, Jian [1 ]
Qian, Canhui [1 ]
Chen, Wei [2 ]
Huang, Huajie [3 ]
机构
[1] Nanjing Univ Posts & Telecommun NUPT, Coll Sci, New Energy Technol Engn Lab Jiangsu Prov, Nanjing 210023, Peoples R China
[2] Taizhou Univ, Sch Pharmaceut & Chem Engn, Jiaojiang 318000, Zhejiang, Peoples R China
[3] Hohai Univ, Coll Mech & Mat, Nanjing 210098, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
UiO-66-NH2; CuBi2O4; Z-scheme charge-separation mechanism; photodegradation; catalytic activity; antibiotic; ENHANCED PHOTOCATALYTIC PERFORMANCE; ELECTRONIC-STRUCTURE; HYDROGEN EVOLUTION; DEGRADATION; HETEROJUNCTION; FABRICATION; COMPOSITES; DESIGN; TIO2;
D O I
10.1021/acsanm.3c03862
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Unidimensional (1D) CuBi2O4@two-dimensional (2D) UiO-66-NH2 core-shell nanostructures were rationally fabricated by decorating thin-layered UiO-66-NH2 on the surface of CuBi2O4 nanorods for improving photodegradation activities toward removing tetracycline hydrochloride (TCH). A high tetracycline TCH photodegradation efficiency was achieved for the CuBi2O4@UiO-66-NH2(0.2) sample, with a kinetic degradation constant of up to 0.0126 min(-1), which is 6.49 and 4.51 times higher than those of bare CuBi2O4 and UiO-66-NH2, respectively, because of the greatly enhanced charge-separation efficiency. Recycling experiments for TCH photodegradation reveal that the CuBi2O4@UiO-66-NH2(0.2) sample is recyclable and relatively stable. The synthesized CuBi2O4@UiO-66-NH2(0.2) sample also exhibits photodegradation activities for the removal of other pharmacologically active compounds (PACs), such as ceftiofur sodium (CS), ciprofloxacin (CIP), and cephalexin (CPX). The efficient charge transfer and improved photocatalytic activity could be attributed to the Z-scheme charge transfer and were verified by band structure analyses, radical-trapping experiments, and electron paramagnetic resonance (EPR) spectra. This investigation could push the design and fabrication of a series of metal-organic frameworks-based core-shell nanostructures toward practical applications of PACs removal.
引用
收藏
页码:20062 / 20073
页数:12
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