首页|Bi2WO6/MIL-101光催化降解水中四环素的性能与机理

Bi2WO6/MIL-101光催化降解水中四环素的性能与机理

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利用水热法制备Bi2WO6/MIL-101(BWO/MIL-101)异质结光催化剂,并研究其在可见光下降解水中四环素(tetracycline;TC)的性能及机理。结果表明,Bi2WO6纳米片在MIL-101载体表面致密生长形成BWO/MIL-101异质结材料后可见光催化TC降解的性能明显提高。其中,结构优化的BWO/MIL-101-40在60min内的TC降解效率为85。9%,其反应速率常数是Bi2WO6的1。4倍,是MIL-101的3。1倍,且BWO/MIL-101在中性及碱性环境中表现出稳定且良好的光催化性能。能带结构分析表明,Bi2WO6/MIL-101构成Ⅱ型异质结,有效拓宽了可见光响应范围,加快光生载流子的迁移速率,并抑制e-和h+的复合。通过自由基猝灭实验和电子顺磁共振(EPR)测试发现,在光催化体系中超氧自由基(·O2-)和空穴(h4)是反应的主要活性物种。
Performance and mechanism of photocatalytic tetracycline degradation by Bi2WO6/MIL-101in water
The Bi2WO6/MIL-101composite photocatalysts were synthesized via a hydrothermal method to facilitate the degradation of tetracycline(TC)under visible light.Research findings demonstrated that the TC degradation efficiency of Bi2WO6 under visible light was significantly enhanced following the dense growth of BWO nanosheets on the surface of MIL-101.Furthermore,the structurally optimized BWO/MIL-101-40exhibited a TC degradation efficiency of 85.9%within 60minutes,with a reaction rate constant approximately 1.4 times that of Bi2WO6 and 3.1times that of MIL-101.Additionally,BWO/MIL-101 displayed consistent and robust photocatalytic performance in neutral and alkaline conditions.Band structure analysis revealed the formation of type Ⅱ heterojunctions between Bi2WO6 and MIL-101,contributing to effective photoelectron-hole separation.Quenching experiments and electron paramagnetic resonance(EPR)tests indicated superoxide radical(·O2-)and holes(h+)as the primary active species in this particular photocatalytic system.

bismuth tungstatemetal-organic frameworktetracyclinephotocatalysisheterojunction

蔡奉颖、许煜航、龙浩然、袁语馨、张宇晴、何秋香、吕健

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福建农林大学资源与环境学院,福建福州 350002

福建福晶科技股份有限公司,福建福州 350003

钨酸铋 金属有机框架 四环素 光催化 异质结

国家自然科学基金资助项目福建省教育厅中青年教师教育科研项目福建农林大学创新基金福建农林大学创新基金

22371042JAT200090CXZX2019073GCXZX2020070A

2024

中国环境科学
中国环境科学学会

中国环境科学

CSTPCDCHSSCD北大核心
影响因子:2.174
ISSN:1000-6923
年,卷(期):2024.44(8)