Self-Assembly of Bi2Sn2O7/?-Bi2O3 S-Scheme Heterostructures for Efficient Visible-Light-Driven Photocatalytic Degradation of Tetracycline

被引:14
作者
Zhu, Baikang [1 ,2 ]
Dong, Qinbin [1 ]
Huang, Jianghua [1 ]
Yang, Mengmeng [1 ]
Chen, Xianlei [3 ]
Zhai, Chunyang [1 ,4 ]
Chen, Qingguo [1 ]
Wang, Bohong [1 ]
Tao, Hengcong [1 ,2 ]
Chen, Li [5 ]
机构
[1] Zhejiang Ocean Univ, Sch Petrochem Engn & Environm, Zhoushan 316022, Peoples R China
[2] Natl & Local Joint Engn Res Ctr Harbor Oil & Gas S, Zhoushan 316022, Peoples R China
[3] Zhoushan Inst Calibrat & Testing Qual & Technol Su, Zhoushan 316000, Zhejiang, Peoples R China
[4] Ningbo Univ, Sch Mat Sci & Chem Engn, Ningbo 315021, Peoples R China
[5] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Gen Practice, Beijing 100036, Peoples R China
基金
中国国家自然科学基金;
关键词
HETEROJUNCTION; COMPOSITE; RAMAN; OXIDATION; WATER; BI; PHOTODEGRADATION; NANOCOMPOSITE; MECHANISMS; NANOSHEETS;
D O I
10.1021/acsomega.2c07899
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Fabrication of S-scheme heterojunctions with enhanced redox capability offers an effective approach to address environmental remediation. In this study, high-performance Bi2Sn2O7/fi-Bi2O3 S-scheme heterojunction photocatalysts were fabricated via the in situ growth of Bi2Sn2O7 on fi-Bi2O3 microspheres. The optimized Bi2Sn2O7/fi-Bi2O3 (BSO/BO-0.4) degradation efficiency for tetracycline hydrochloride was 95.5%, which was 2.68-fold higher than that of fi-Bi2O3. This improvement originated from higher photoelectron-hole pair separation efficiency, more exposed active sites, excellent redox capacity, and efficient generation of center dot O2- and center dot OH. Additionally, Bi2Sn2O7/ fi-Bi2O3 exhibited good stability against photocatalytic degradation, and the degradation efficiency remained >89.7% after five cycles. The photocatalytic mechanism of Bi2Sn2O7/fi-Bi2O3 S-scheme heterojunctions was elucidated. In this study, we design and fabricate high-performance heterojunction photocatalysts for environmental remediation using S-scheme photocatalysts.
引用
收藏
页码:13702 / 13714
页数:13
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