Internal electric field-modulated charge migration behavior in atom co-sharing Bi2S3/Bi2Sn2O7 heterojunction for efficient

被引:0
|
作者
Tian, Fengyu [1 ]
Li, Yaohao [1 ]
Miao, Wei [1 ]
Liang, Jiayu [1 ]
Rodriguez, Diana Vanessa Cordero [1 ]
Yan, Xuemin [1 ]
机构
[1] Yangtze Univ, Coll Chem & Environm Engn, Jingzhou 434023, Peoples R China
关键词
in-situ fabrication; Atom co-sharing; Photocatalytic tetracycline degradation; Internal electric field; PHOTOCATALYTIC ACTIVITY; DEGRADATION; TRANSFORMATION; FABRICATION; REDUCTION; REMOVAL;
D O I
10.1016/j.surfin.2025.106280
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
Developing highly efficient and visible-light responsive Bi2Sn2O7-based photocatalysts for diverse pollutants removal has attracted considerable attention. In this work, Bi2S3/Bi2Sn2O7 heterostructure photocatalyst with co-shared Bi atoms was fabricated through an in-situ sulfuration process. Experimental studies and theoretical calculations verified that the co-sharing of Bi atoms through O-Bi-S bonds across the interface and the internal electric field (IEF) between Bi2Sn2O7 and Bi2S3 can transform the type-I charge transfer process into an IEFmodulated charge migration behavior, significantly enhancing charge separation efficiency. Additionally, the incorporation of Bi2S3 broadened the visible light absorption range. Consequently, the optimal Bi2S3/Bi2Sn2O7 heterostructure exhibited a remarkable enhancement in photocatalytic tetracycline degradation activities compared to pure Bi2S3 and Bi2Sn2O7. This work provides valuable guidance for the rational design of highly-efficient Bi-based heterojunctions for photocatalytic environmental remediation.
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页数:9
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