Heterojunction Cu2O/RGO/BiVO4 ternary nanocomposites with enhanced photocatalytic activities towards degradation of rhodamine B and tetracycline hydrochloride

被引:18
作者
Hu, Xiaoying [1 ,2 ]
Zhang, Qi [1 ,2 ]
Nan, Haoshan [1 ,2 ]
Wang, Ming [1 ,2 ]
Qiao, Liang [1 ,2 ]
Tian, Hongwei [3 ,4 ]
机构
[1] Changchun Univ, Coll Sci, Changchun 130022, Jilin, Peoples R China
[2] Changchun Univ, Lab Mat Design & Quantum Simulat, Changchun 130022, Jilin, Peoples R China
[3] Jilin Univ, Key Lab Automobile Mat MOE, Changchun 130012, Jilin, Peoples R China
[4] Jilin Univ, Sch Mat Sci & Engn, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
CORE-SHELL STRUCTURE; CATALYTIC-ACTIVITY; WATER OXIDATION; LIGHT; PERFORMANCE; COMPOSITE; GRAPHENE; BIVO4; CONSTRUCTION; FABRICATION;
D O I
10.1039/c9nj04351a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Compared to the traditional type II heterojunction photocatalyst (Cu2O/BiVO4), bulk BiVO4 was modified in this study by reduced graphene oxide (RGO) with a Schottky structure to optimize the coupling interface of BiVO4. Cu2O nanoparticles were then grown in situ on the RGO/BiVO4 surface to yield a heterojunction structure with an internal electric field, allowing movement of photogenerated electrons and holes in opposite directions to participate in redox reactions. The as-obtained optimized Cu2O/RGO/BiVO4 material exhibited excellent photocatalytic degradation performance towards organic pollutants. The reaction rate constant of rhodamine B (RhB) was estimated as 0.0324 min(-1), which was almost 5.94, 5.15 and 1.94-fold higher than those of bare BiVO4, 4%RGO/BiVO4 and 5%Cu2O/BiVO4, respectively. Moreover, the optimized material displayed good activity in the degradation of the colorless organic contaminant tetracycline hydrochloride (TC). The reaction rate constant was estimated as 0.0219 min(-1), which was almost 1.6-, 1.4- and 1.63-fold higher than those of bare BiVO4, 4%RGO/BiVO4 and 5%Cu2O/BiVO4, respectively. The hole and superoxide radical worked as active species for degradation of organic matter. Such a significant increase in degradation efficiencies was attributed not only to the formation of a heterojunction structure but also to rapid electron transfer between interfaces.
引用
收藏
页码:18240 / 18250
页数:11
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