Three-dimensional Z-Scheme Ag3PO4/Co3(PO4)2@Ag heterojunction for improved visible-light photocatalytic degradation activity of tetracycline

被引:98
|
作者
Shi, Weilong [1 ]
Li, Mingyang [3 ]
Huang, Xiliu [3 ]
Ren, Hongji [3 ]
Guo, Feng [2 ]
Yan, Chao [1 ]
机构
[1] Jiangsu Univ Sci & Technol, Sch Mat Sci & Engn, Zhenjiang 212003, Jiangsu, Peoples R China
[2] Jiangsu Univ Sci & Technol, Sch Energy & Power, Zhenjiang 212003, Jiangsu, Peoples R China
[3] Jiangsu Univ Sci & Technol, Sch Environm & Chem Engn, Zhenjiang 212003, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Co-3(PO4)(2); Ag3PO4; Ag nanoparticles; Heterostructure; Z-Scheme; OXYGEN EVOLUTION; COMPOSITE PHOTOCATALYST; HYBRID PHOTOCATALYST; QUANTUM DOTS; EFFICIENT; PERFORMANCE; FABRICATION; MICRORODS; NANOSHEETS; MECHANISM;
D O I
10.1016/j.jallcom.2019.152883
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Constructing Z-scheme photocatalyst is paramount to improve the photocatalytic activity of single semiconductor materials by the efficient separation of photo-generated carriers. Herein, a novel Zscheme photocatalyst Ag3PO4/Co-3(PO4)(2)@Ag was successfully synthesized, which has the distinctive three dimensional (3D) structure with the Ag3PO4 rhombic dodecahedrons on the flower-like Co-3(PO4)(2). The ternary Ag3PO4/Co-3(PO4)(2)@Ag heterostructure photocatalyst exhibits the highest photocatalytic activity in comparison with Ag3PO4, Co-3(PO4)(2) and Ag3PO4/Co-3(PO4)(2), which can be up to 91.2% at 60 min for the degradation of tetracycline (TC) under visible light irradiation. This enhanced photocatalytic performance is attributed to the surface plasmon resonance (SPR) of Ag to effectively broaden the absorption of visible light in composites, which is proved by the finite-difference time domain (FDTD) simulation. Moreover, the results of electron spin resonance (ESR) confirmed that the introduction of Ag nanoparticles can further facilitate the charge transfer of heterostructure Ag3PO4/Co-3(PO4)(2) through the route of the Z-scheme, fully retaining prominent redox ability of Ag3PO4 and Co-3(PO4)(2). Finally, the possible photocatalytic degradation mechanism over Ag3PO4/Co-3(PO4)(2)@Ag was proposed and discussed in detail. (C) 2019 Elsevier B.V. All rights reserved.
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页数:10
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