Atomically thin Bi/Bi4Ti3O12 heterojunction mediated increasing active photogenerated carriers for boosting photocatalytic activity

被引:33
|
作者
Liu, Tong [1 ]
Cheng, Zhiyuan [1 ]
Shi, Tian [1 ]
Yang, Shenghong [1 ]
Zhang, Yueli [1 ]
机构
[1] Sun Yat Sen Univ, Sch Mat Sci & Engn, Sch Phys, State Key Lab Optoelect Mat & Technol, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalytic; Bi/Bi4Ti3O12 2D ultrathin heterojunction; Internal electric field; Charge separation; Degradation; METAL-FREE PHOTOCATALYST; CO2; PHOTOREDUCTION; OXYGEN VACANCIES; CONTROLLABLE SYNTHESIS; EXCITON DISSOCIATION; HIGHLY EFFICIENT; 001; FACETS; NANOSHEETS; CONVERSION; BIOBR;
D O I
10.1016/j.jcis.2022.01.048
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
Two-dimensional (2D) semiconductors play an essential role in the field of photocatalytic repairing environment on account of their unique electronic structure and ultra-high specific surface area. Here, a 1-2-layer 2D ultrathin Bi/Bi4Ti3O12 (BTO-U-B2) heterojunction photocatalyst is constructed, and the delivery mechanism of electronic is proposed based on photoelectric performance and theoretical calculation results. The efficiency of separation, transfer and recombination of photogenerated carriers is considerably improved due to the enhanced internal electric field, shorter transfer distance and the introduction of electron traps, respectively. Moreover, bisphenol A (BPA) degradation rate of BTO-U-B2 heterojunction under xenon lamp is 9.06 and 2.57 times higher than that of Bi4Ti3O12 microplates and nanosheets, respectively. The enhanced photocatalytic activity benefits from the synergistic effect of 2D ultrathin structure and surface heterojunction. Additionally, the photocatalysis test are performed by replacing different environmental solutions and various organic pollutants, and results reveal that this heterojunction has a certain applicability. This work provides a deep insight into designing efficient 2D heterojunction photocatalysis. (C) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:625 / 635
页数:11
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