Synthesis of graphene-based CdS@CuS core-shell nanorods by cation-exchange for efficient degradation of ciprofloxacin

被引:34
|
作者
Zhao, Yitao [1 ,2 ]
Zuo, Yuanjie [1 ]
He, Guangyu [1 ]
Chen, Qun [1 ]
Meng, Qi [1 ]
Chen, Haiqun [1 ]
机构
[1] Changzhou Univ, Adv Catalysis & Green Mfg Collaborat Innovat Ctr, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
[2] Changzhou Vocat Inst Text & Garment, Changzhou Key Lab New Text Mat, Changzhou 213164, Peoples R China
基金
中国国家自然科学基金;
关键词
CdS@CuS/RGO; Solvothermal method; Cation-exchange; Core-shell nanorods; Photocatalysis; ENHANCED PHOTOCATALYTIC ACTIVITY; HIGH-PERFORMANCE; OXIDE; EVOLUTION; CONSTRUCTION; COMPOSITES; HYBRID;
D O I
10.1016/j.jallcom.2021.159305
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
Reduced graphene oxide (RGO) supported CdS@CuS core-shell nanorods (CdS@CuS/RGO) were prepared by a simple, solvothermal method involving cation-exchange for efficient degradation of the fluoroquinolone antibiotic, ciprofloxacin (CIP). CdS@CuS/RGO delivers superior photocatalytic degradation of CIP in simulated sunlight. Ascribed to the unique nanostructure, the CIP degradation efficiency of CdS@CuS/RGO reaches 91.5%, which is higher than that of CdS (67.1%) alone. Compared with previously reported catalysts, CdS@CuS/RGO exhibits higher degradation efficiency in less time and lower dosage. Furthermore, its degradation efficiency remains at around 81.5% after five usage cycles, which represents excellent cycling stability. Free radical scavenging experiments show that superoxide radicals and holes play important roles in the degradation. The CdS@CuS/RGO utilizes the synergistic effects of CdS, CuS and RGO to effectively retard the photo corrosion of CdS upon visible light exposure, reduce the band-gap energy, suppress the recombination of photo-generated electron-hole pairs and promote the adsorption of catalyst toward CIP, thereby, enhancing the catalytic performance of the composite. (C) 2021 Elsevier B.V. All rights reserved.
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页数:9
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