Construction of Br-Cu2O@NiFe-LDHs Z-scheme heterojunction and photocatalytic degradation of catechol

被引:2
|
作者
Chen, Zhuying [1 ]
Huang, Zhiling [2 ]
Meng, Yue [2 ]
Xie, Bo [1 ]
Ni, Zheming [1 ]
Xia, Shengjie [1 ]
机构
[1] Zhejiang Univ Technol, Dept Chem, Coll Chem Engn, Hangzhou 310014, Peoples R China
[2] Huzhou Coll, Sch Life & Hlth Sci, Dept Pharmaceut Engn, Huzhou 313000, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Br doping; Layered double hydroxides; Z -scheme heterojunction; Facet regulation; Built in electric field; CU2O;
D O I
10.1016/j.jece.2024.113686
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Facet regulation and construction of heterojunctions are important means to enhance the photocatalytic performance of single-phase materials. In this paper, the facet index of Cu2O 2 O was changed through Br doping, and then a Br doped Cu2O@NiFe-LDHs 2 O@NiFe-LDHs Z-scheme heterojunction (BC@LDHs) was constructed for photocatalytic degradation of catechol. The optimal conditions for photocatalytic degradation reaction were explored; the kinetic and thermodynamic parameters of the reaction, as well as the stability and reusability of the material were studied. Under optimal reaction conditions, the photocatalytic degradation of catechol can reach up to 95.68 % by BC@LDHs, which is much higher than that of single-phase materials and Cu2O@LDHs. 2 O@LDHs. By combining experiments and theoretical calculations, the intrinsic reasons and mechanisms for Br doping to enhance the photocatalytic degradation performance of BC@LDHs Z-scheme heterojunctions were fully explored from the perspectives of band structure and oxygen adsorption, determination of built-in electric field in Z-scheme heterojunctions, calculation of built-in electric field strength and bulk charge separation efficiency. This work proposes the insights that using Br doping to alter exposed facets and regulate the strength of the built-in electric field in Br-Cu2O@NiFe-LDHs 2 O@NiFe-LDHs heterojunctions, thereby promoting its efficient photocatalytic degradation.
引用
收藏
页数:15
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