Hierarchical heterostructures of p-type bismuth oxychloride nanosheets on n-type zinc ferrite electrospun nanofibers with enhanced visible-light photocatalytic activities and magnetic separation properties

被引:41
|
作者
Sun, Yucong
Shao, Changlu [1 ]
Li, Xinghua [1 ]
Guo, Xiaohui
Zhou, Xuejiao
Li, Xiaowei
Liu, Yichun
机构
[1] Northeast Normal Univ, Minist Educ, Ctr Adv Optoelect Funct Mat Res, 5268 Renmin St, Changchun 130024, Jilin, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
ZnFe2O4; nanofiber; BiOCl nanosheet; p-n heterojunction; Hierarchical structure; Photocatalysis; Magnetic separation; TIO2; NANOFIBERS; DEGRADATION; EFFICIENT; DYE; IDENTIFICATION; MICROSPHERES; FABRICATION; COMPOSITES; BI2WO6; BIOCL;
D O I
10.1016/j.jcis.2018.01.033
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
P-type bismuth oxychloride (p-BiOCl) nanosheets were uniformly grown on n-type zinc ferrite (n-ZnFe2O4) electrospun nanofibers via a solvothermal technique to form hierarchical heterostructures of p-BiOCl/n-ZnFe2O4 (p-BiOCl/n-ZnFe2O4 H-Hs). The density and loading amounts of the BiOCl nanosheets with exposed {001} facets were easily controlled by adjusting the reactant concentration in the solvothermal process. The p-BiOCl/n-ZnFe2O4 H-Hs exhibited enhanced visible-light photocatalytic activities for the degradation of Rhodamine B (RhB). The apparent first-order rate of the p-BiOCl/n-ZnFe2O4 H-Hs and its normalized constant were about 12.6- and 8-fold higher than pure ZnFe2O4 nanofibers. This suggests that both the improved charge separation efficiency from the uniform p-n heterojunctions and the enlarged active surface sites from the hierarchical structures increase the photocatalytic performances. Furthermore, the p-BiOCl/n-ZnFe2O4 H-Hs could be efficiently separated from the solution with an external magnetic field via the ferromagnetic behavior of ZnFe2O4 nanofibers. The magnetic p-BiOCl/n-ZnFe2O4 H-Hs with enhanced visible-light photocatalytic performances might have potential applications in water treatment. (C) 2018 Published by Elsevier Inc.
引用
收藏
页码:110 / 120
页数:11
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