Novel direct dual Z-scheme AgBr(Ag)/MIL-101(Cr)/CuFe2O4 for efficient conversion of nitrate to nitrogen

被引:35
|
作者
Li, Zhaoyang [1 ,2 ]
Zhao, Yongjie [1 ]
Guan, Qing [1 ]
Liu, Qian [1 ]
Khan, Sara [1 ]
Zhang, Leilei [1 ]
Wang, Xianze [1 ]
Chen, Lei [1 ]
Yang, Xia [1 ]
Huo, Mingxin [1 ]
机构
[1] Northeast Normal Univ, Sch Environm, Jingyue St 2555, Changchun 130117, Peoples R China
[2] Tongji Architectural Design Grp Co Ltd, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
AgBr(Ag)/MIL-101(Cr)/CuFe2O4; Magnetism; Photoreduction; Nitrate; Dual Z-scheme; ENHANCED PHOTOCATALYTIC ACTIVITY; VISIBLE-LIGHT PHOTOCATALYST; REDUCTION; COMPOSITE; PERFORMANCE; WATER; CONSTRUCTION; DEGRADATION; ADSORPTION; NANOPARTICLES;
D O I
10.1016/j.apsusc.2019.145225
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 nitrate has attracted much attention recently, however, low efficiency and difficult separation have limited its application in practice. In this study, the novel direct dual Z-scheme AgBr(Ag)/MIL-101(Cr)/CuFe2O4 (AB/M/CFO) was fabricated by the hydrothermal technology combined with the photodeposition method for the first time. The AB/M/CFO exhibited the highest nitrate conversion and nitrogen selectivity (79.9% and 94.5%, respectively) compared to AgBr(Ag)/MIL-101(Cr), MIL-101(Cr) and CuFe2O4 for 30 min UV-light irradiation. The dual Z-scheme of AB/M/CFO enhanced electron transfer and charge separation, which was proved by transient photocurrent responses, leading to a significant improvement in photocatalytic efficiency. Meanwhile, after four cycles, the AB/M/CFO photocatalyst also displayed a strong magnetic separation ability and excellent recycling stability. Furthermore, the excitation and electron transfer process over dual Z-scheme AB/M/CFO photocatalytic material were proposed, based on the radical trapping experiments. Our work provides a new strategy to construct dual Z-scheme MOFs-based materials that have promising applications in photocatalytic reduction of pollutants.
引用
收藏
页数:11
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