A novel hierarchical BaTiO3/AgI heterojunction with boosting spatial charge kinetics for photocatalytic degradation of organic pollutant

被引:28
作者
He, Chenpu [1 ]
Jing, Panpan [1 ]
Wang, Peifeng [1 ]
Ji, Jiamin [1 ]
Ouyang, Tao [1 ]
Cui, Yongfei [1 ]
Pu, Yongping [1 ]
机构
[1] Shaanxi Univ Sci & Technol, Shaanxi Key Lab Green Preparat & Functionalizat I, Sch Mat Sci & Engn, Xian 710021, Shaanxi, Peoples R China
关键词
BaTiO3; AgI; Ag medium; Hierarchical microstructure; Heterojunction photocatalyst; Rhodamine B; Spatial charge kinetics; Z-SCHEME PHOTOCATALYST; LIGHT; NANOPARTICLES; EFFICIENT; REDUCTION;
D O I
10.1016/j.ceramint.2021.08.249
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A novel BaTiO3/AgI heterojunction with a three-dimensional (3D) hierarchical microstructure was synthesized via a hydrothermal and in-situ co-precipitation route. As a photocatalyst, the BaTiO3/AgI heterojunction exhibited an optimal Rhodamine B (RhB) removal performance (92.2%) under the visible-light irradiation within 15 min, which was 82.3 and 3.7 times of the pure BaTiO3 and AgI, respectively. The superior photocatalytic activity was achieved by the considerable specific surface area of hierarchical microstructure, reinforced visiblelight response ability and promoted spatial separation efficiency of photo-induced carriers by heterojunction interface. It was suggested that small amount of Ag nanoparticles reduced in-situ on the BaTiO3/AgI heterojunction surface during the photocatalytic reaction process could act as an electronic transfer medium for promoting the photo-induced electrons on conduction band (ECB) of AgI. Therefore, a typical spatial charge transfer mechanism of the BaTiO3/AgI heterojunction was proposed. Moreover, this current work can significantly provide a new insight of the BaTiO3-based photocatalysts for the efficient environmental governance and energy utilization.
引用
收藏
页码:33426 / 33434
页数:9
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