BiOBr microspheres anchored with Cu2O nanoparticles and rGO: A Z-scheme heterojunction photocatalyst for efficient reduction of Cr(VI) under visible light irradiation

被引:13
|
作者
Ma, Jian [1 ]
Liang, Congjie [1 ]
Yu, Changjiang [1 ]
Li, Huaming [1 ,2 ]
Xu, Hui [2 ]
Hua, Yingjie [1 ]
Wang, Chongtai [1 ]
机构
[1] Hainan Normal Univ, Sch Chem & Chem Engn, Key Lab Electrochem Energy Storage & Energy Conver, Key Lab Electrochem Energy Storage & Light Energy, Haikou 571158, Peoples R China
[2] Jiangsu Univ, Sch Environm & Safety Engn, Inst Energy Res, Zhenjiang 212013, Peoples R China
基金
海南省自然科学基金;
关键词
Cu2O; rGO; BiOBr; Z-scheme heterojunction; Synergy effect; Photocatalysis; Cr(VI) reduction; FACET-DEPENDENT PERFORMANCE; OXYGEN-VACANCY; GRAPHENE OXIDE; H-2; EVOLUTION; REMOVAL; FABRICATION; NANOSHEETS; G-C3N4; NANOCOMPOSITES; PHOTOREDUCTION;
D O I
10.1016/j.apsusc.2022.155247
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
Photocatalytic reduction of hexavalent chromium (Cr(VI)) is an effective way to reduce its environmental risk. However, it remains a challenge to achieve a high removal rate in mild conditions. In order to efficiently remove Cr(VI) from water, a novel Z-scheme heterojunction composite photocatalyst rCB-20 (Cu2O/rGO/BiOBr, 20% Cu2O) was successfully prepared using a simple two-step strategy in this work. The characterizations of the catalyst show that the Z-scheme heterojunction formed between Cu2O and BiOBr is favorable for facilitating the separation of photogenerated carriers. The existence of rGO can reduce the resistance of electron transport. Therefore, the composite photocatalyst exhibits a very high photocatalytic activity in the photoreduction of Cr (VI). For example, using it to completely remove Cr(VI) with a concentration of 20 mg center dot L-1 in the pH = 4 solution only requires 40 min. Even the complete removal of the same concentration of Cr(VI) in neutral water at pH 7 does not take more than 90 min. Meanwhile, it possesses a high stability in catalytic activity and structure.
引用
收藏
页数:11
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