Synthesis and Photocatalytic Activity of Z-Scheme Photocatalyst Sb2WO6/g-C3N4

被引:0
作者
Zhang Jing [1 ]
Dong Yuming [1 ]
Liu Xiang [1 ]
Li Hexing [2 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Minist Educ, Key Lab Synthet & Biol Colloids, Wuxi 214122, Peoples R China
[2] Shanghai Normal Univ, Chinese Minist Educ Resource Chem, Key Lab, Shanghai 200234, Peoples R China
来源
CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE | 2019年 / 40卷 / 01期
基金
中国国家自然科学基金;
关键词
Sb2WO6/g-C3N4; Z-Scheme photocatalyst; Photocatalytic activity; GRAPHITIC CARBON NITRIDE; DEGRADATION; PERFORMANCE; HETEROJUNCTION; FABRICATION; G-C3N4; COMPOSITES; ADSORPTION; NANOSHEETS;
D O I
10.7503/cjcu20180498
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Sb2WO6 modified g-C3N4 (Sb2WO6/g-C3N4) composites were synthesized by hydrothermal reaction. The properties of the Sb2WO6/g-C3N4 composites were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM) , UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS) and photoluminescence( PL) spectroscopy. The results indicated that the Sb2WO6 grew on the surface of g-C3N4, forming closely contacted interfaces between the Sb2WO6 and g-C3N4 components. The photocatalytic performance of Sb2WO6/g-C3N4 composites was evaluated through the photodegradation of Rhodamine B (RhB). The results showed that 99. 3% of RhB was degraded by Sb2WO6/g-C3N4 composites with 10% (mass fraction) of Sb2WO6 in 60 min under simulated sunlight, which was much higher than that of pure g-C3N4 and Sb2WO6. This highly enhanced photocatalytic activity of the Sb2WO6/g-C3N4 composites can be mainly attributed to strong interfacial interaction promoting the photo-generated electron-hole separation and migration. The results of radical scavenger experiments showed that center dot O-2(-) and h(+) were the dominant reactive species in the photocatalytic reaction. Besides, the Sb2WO6/g-C3N4 composites showed excellent stability over several reaction cycles. Finally, a possible Z-scheme photocatalytic mechanism was proposed based on the experimental results.
引用
收藏
页码:123 / 129
页数:7
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