Carbon Doping and Oxygen Vacancy-Tungsten Trioxide/Cu3SnS4 S-Scheme Heterojunctions for Boosting Visible-Light-Driven Photocatalytic Performance

被引:0
|
作者
Zhang, Na [1 ]
Wang, Yichao [1 ]
Xing, Zipeng [1 ]
Li, Zhenzi [2 ]
Zhou, Wei [2 ]
机构
[1] Heilongjiang Univ, Sch Chem & Mat Sci, Dept Environm Sci, Minist Educ Peoples Republ China,Key Lab Funct Ino, Harbin 150080, Peoples R China
[2] Qilu Univ Technol, Shandong Acad Sci, Sch Chem & Chem Engn, Shandong Prov Key Lab Mol Engn, Jinan 250353, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
photocatalysis; S-scheme heterojunction; oxygenvacancy; carbon doping; tungsten trioxide; Cu3SnS4; CU3SNS4; ACTIVATION; COMPOSITE; REMOVAL; CO2;
D O I
10.1021/acsami.4c22048
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Developing ideal photocatalysts for energy regeneration and environmental remediation by combining the advantages of individual semiconductors remains a significant challenge. Herein, tungsten trioxide (WO3)/Cu3SnS4 S-scheme heterojunction composite photocatalysts are developed. Initially, doped oxygen vacancy (OV) was prepared on two-dimensional WO3 nanosheets by direct calcination method. Subsequently, Cu3SnS4 nanoflowers are produced via a one-step hydrothermal process, which are then used to wrap the WO3 nanosheets. The close contact between WO3 and Cu3SnS4, coupled with unsaturated C-OV coordination, enhanced the interfacial electron transport. Under visible light irradiation, the WO3/Cu3SnS4 shows an impressive H-2 production rate of 3345.26 mu mol h(-1) g(-1), a significant improvement over the individual performances of WO3 and Cu3SnS4. Moreover, WO3/Cu3SnS4 demonstrated the highest photocatalytic tetracycline degradation efficiency, achieving 99.4% degradation within 90 min of illumination. An efficient S-scheme heterojunction system with a well-aligned band structure was successfully constructed. This design effectively extends their lifetime, allowing the heterojunction to achieve maximum efficiency in the light reaction.
引用
收藏
页码:18296 / 18306
页数:11
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