Crystal face-selective Bi4Ti3O12/BiOI heterojunction constructed for enhanced visible ligtht-driven photocatalytic activity

被引:34
作者
Liu, Tong [1 ]
Li, Yongjin [1 ]
Cheng, Zhiyuan [1 ]
Peng, Yan [1 ]
Shen, Menghan [1 ]
Yang, Shenghong [1 ]
Zhang, Yueli [1 ]
机构
[1] Sun Yat Sen Univ, Sch Mat Sci & Engn, State Key Lab Optoelect Mat & Technol, Sch Phys, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalytic; Bi4Ti3O12/BiOI heterojunction; Ferroelectric; Spontaneous polarization; CO2; PHOTOREDUCTION; OXYGEN VACANCIES; PERFORMANCE; NANOSHEETS; BIOI; HETEROSTRUCTURES; NANOPARTICLES; CONVERSION; ER3+;
D O I
10.1016/j.apsusc.2021.149507
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
Spontaneous polarization of ferroelectric is used to promote the separation of photogenerated electrons and holes, showing tremendous potentials of solar-light driven photocatalytic. However, designing a system of efficient response to visible light, remains a fundamental challenge due to rapid recombination of electrons-holes and weak absorption in visible region. Here, we synthetized Bi4Ti3O12/BiOI heterojunction, which BiOI nanosheets selectively deposited on (110) facets of Bi4Ti3O12 by epitaxy growth. The synthetized heterojunction is characterized by phase structures, morphology, and surface chemical state. The results of ferroelectric phase curve illustrate that the construction of heterojunction enhances the ferroelectric properties, which is favorable to improve the separation and recombination processes of carriers. Furthermore, the sample Bi4Ti3O12/BiOI-3 reveals better photocatalytic kinetics in photodegradation of bisphenol A (BPA) under visible-light irradiation, which is about 74.16 and 1.83 times faster than that of pure Bi4Ti3O12 and BiOI. This work provides an effective and scalable strategy for designing a system of efficient response to visible light.
引用
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页数:9
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