Visible light active CdS@TiO2 core-shell nanostructures for the photodegradation of chlorophenols

被引:34
作者
Al-Fandi, Thuraya [1 ]
Al Marzouqi, Faisal [1 ]
Kuvarega, Alex T. [2 ]
Mamba, Bhekie B. [2 ]
Al Kindy, Salma M. Z. [1 ]
Kim, Younghun [3 ]
Selvaraj, Rengaraj [1 ]
机构
[1] Sultan Qaboos Univ, Coll Sci, Dept Chem, POB 36,PC 123, Muscat, Oman
[2] Univ South Africa, Coll Sci Engn & Technol, Nanotechnol & Water Sustainabil Res Unit, Florida Sci Campus, Johannesburg, South Africa
[3] Kwangwoon Univ, Dept Chem Engn, Seoul 139701, South Korea
关键词
Chlorophenol; Core-shell structure; Photocatalysis; Visible light; CdS@TiO2; PHOTOCATALYTIC ACTIVITY; CDS; NANOCRYSTALS; NANOSPHERES; OXIDATION; ANATASE;
D O I
10.1016/j.jphotochem.2019.01.019
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
The presence of chlorophenols in various environmental media has become a human health concern. In this study, homogeneous cadmium sulfide (CdS) sub-microspheres were prepared through a solution phase and hydrothermal method, form cadmium acetate dihydrate and thiourea. CdS@TiO2 core-shell nanostructures were synthesized using the as prepared CdS (1:4), through two steps including the solution phase and hydrothermal methods. The prepared CdS sub-microspheres and CdS@TiO2 were characterized using a number of physicochemical techniques such as X-ray diffraction (XRD), RAMAN spectroscopy, X-ray photoelectron spectroscopy (XPS), UV-vis Diffuse Reflectance Spectroscopy (UV-vis DRS), Scanning Electron Microscopy (SEM), Transmission Electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). The experimental results demonstrated that the morphology of the CdS sub-microspheres can be easily controlled by changing the ratio of cadmium acetate/thiourea. The SEM analysis revealed that the CdS sub-microspheres prepared by solution phase and hydrothermal methods possess an average size of around 149 and 470 nm respectively. The CdS sub-microspheres and CdS@TiO2 core-shell materials were evaluated for the visible light photocatalytic degradation of 2,4-dichlorophenol and 2,4,6-trichlorophenol. CdS@TiO2 showed up to 20% enhanced photo catalytic activity for the degradation of 2,4-DCP and 2,4,6-TCP compared to pure CdS. Up to 70% of 2,4-DCP and 2,4,6-TCP were removed in 6 h. The enhanced photoactivity can be attributed to the longer lifetime of photogenerated electron - hole pairs from the CdS@TiO2 compared to the pure CdS material.
引用
收藏
页码:75 / 83
页数:9
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