Hierarchical N-doped TiO2@Bi2WxMo1-xO6 core-shell nanofibers for boosting visible-light-driven photocatalytic and photoelectrochemical activities

被引:70
作者
Ghoreishian, Seyed Majid [1 ]
Ranjith, Kugalur Shanmugam [2 ]
Lee, Hoomin [1 ]
Ju, Hong-il [1 ]
Nikoo, Somayeh Zeinali [3 ]
Han, Young-Kyu [2 ]
Huh, Yun Suk [1 ]
机构
[1] Inha Univ, Dept Biol Engn, Biohybrid Syst Res Ctr, Incheon 22212, South Korea
[2] Dongguk Univ Seoul, Dept Energy & Mat Engn, Seoul 04620, South Korea
[3] Kharazmi Univ, Fac Chem, Dept Organ Chem, Tehran, Iran
基金
新加坡国家研究基金会;
关键词
Core-shell nanofibers; Photocatalysis; Visible-light; Antibiotic; Electrospinning; CATALYTIC DEGRADATION; TETRACYCLINE; HETEROJUNCTION; NANOCOMPOSITE; PERFORMANCE; BI2WO6; FABRICATION; COMPOSITE; G-C3N4; PHOTOACTIVITY;
D O I
10.1016/j.jhazmat.2020.122249
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Heterogeneous photocatalysis has been proven to be a promising approach to overcome the great challenges encountered with conventional technologies for environmental remediation. Herein, for the first time, a novel hierarchical architecture of nitrogen-doped TiO2@Bi2WxMo1-xO6, x = 0-1.0) was rationally designed and fabricated through an electrospinning route followed by a solvothermal process. The photocatalytic activity of the as-prepared samples was evaluated based on the degradation of tetracycline hydrochloride (TC) under visible-light irradiation. The results indicated that the molar fraction of W/Mo has a strong impact on the photocatalytic efficiency and photoelectrochemical performance of the N-T@BWMO composites. Compared to N-TiO2 and the binary composites, N-T@BWMO-0.25 exhibited outstanding photocatalytic activity and significant cycling stability. The enhanced photocatalytic activity can be synergistically linked to the excellent native adsorption, extended light-harvesting region, hierarchical structure, and strong interfacial interaction between N-TiO2 and BWMO, which can effectively prolong the lifetime of charge-carriers. Moreover, active species-trapping and electron paramagnetic resonance results confirmed that holes and superoxide radicals were the dominant active species responsible for TC removal. A possible photocatalytic mechanism underlying the degradation of TC by N-T@BWMO-0.25 is also proposed. We expect that our findings will provide new insights into the use of highly efficient core-shell heterostructure photocatalysts, with potential applications in environmental decontamination.
引用
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页数:17
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