One-pot fabrication of Bi3O4Cl/BiOCl plate-on-plate heterojunction with enhanced visible-light photocatalytic activity

被引:142
|
作者
Ning, Shangbo [1 ]
Ding, Luyao [1 ]
Lin, Zheguan [1 ]
Lin, Qianying [1 ]
Zhang, Hualei [1 ]
Lin, Huaxiang [1 ]
Long, Jinlin [1 ]
Wang, Xuxu [1 ]
机构
[1] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
关键词
Bi3O4Cl/BiOCl; Heterostructure; Visible light; Photocatalysis; Orange II; SOLVOTHERMAL SYNTHESIS; HYDROTHERMAL SYNTHESIS; BIOCL PHOTOCATALYST; MODEL COMPOUNDS; PERFORMANCE; NANOSTRUCTURES; IRRADIATION; COMPOSITES; PHOTODEGRADATION; NANOCOMPOSITE;
D O I
10.1016/j.apcatb.2015.12.021
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
Bi3O4Cl/BiOCl (B3O4C/BOC) heterojunction photocatalyst with high visible-light photocatalytic activity was synthesized by one-pot hydrothermal method. The morphology, crystal, structure, optical and photo catalytic property of the synthesized samples were characterized by XRD, SEM, HRTEM, EDX, BET, UV-vis DRS, photocurrent, PL, and etc. The B3O4C/BOC heterojunction photocatalyst exhibited higher photocatalytic activity than pure BiOCl (BOC) and Bi3O4Cl (B3O4C) for the degradation of Orange II under visible light (lambda >= 420 nm). The 0.50B(3)O(4)C/BOC-1 heterojunction exhibited the highest photocatalytic activity and its photocatalytic efficiency was 4.4-fold more than those of pure BOC. In addition, the 0.50B(3)O(4)C/BOC-1 synthesized by one-pot hydrothermal method exhibited higher photocatalytic activity than that prepared by two-step traditional synthesis method. The enhanced photocatalytic activity of the B3O4C/BOC heterostructure photocatalyst was predominantly attributed to the efficient separation of photoinduced electrons and holes. Ultimately, the results also reveal that (OH)-O-center dot and center dot O2- radicals are primarily reactive species in the photocatalytic system, which are the key factors responsible for the nearly complete mineralization of Orange II. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:203 / 212
页数:10
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