Bi2Sn2O7/CeO2Z型异质结光催化剂在可见光下降解有机污染物性能研究

王妮都, 汪业勇, 王逸菲, 沈正千, 黄江华, 竺柏康, 杨淑清

现代化工 ›› 2024, Vol. 44 ›› Issue (3) : 175 -181.

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现代化工 ›› 2024, Vol. 44 ›› Issue (3) : 175-181. DOI: 10.16606/j.cnki.issn0253-4320.2024.03.031
科研与发展

Bi2Sn2O7/CeO2Z型异质结光催化剂在可见光下降解有机污染物性能研究

    王妮都, 汪业勇, 王逸菲, 沈正千, 黄江华, 竺柏康, 杨淑清
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Degradation of organic pollutants by Bi2Sn2O7/CeO2 Z-type heterojunction photocatalyst in visible light

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摘要

利用水热法将Bi2Sn2O7纳米颗粒负载到CeO2微球上制备Z型异质结光催化剂并用于光催化降解水污染物。结果表明,在光照下60min时,优化的Bi2Sn2O7/CeO2(BSC-5)对盐酸四环素的降解效率达到88.4%(反应速率常数k=0.0334 min-1),是CeO2的8.25倍和Bi2Sn2O7的4.71倍。Z型异质结可以形成更多暴露的活性中心,具有更好的光电子-空穴对分离效率、优异的氧化还原能力以及有效产生超氧自由基(·O-2)和羟基自由基(·OH)。此外,Bi2Sn2O7/CeO2在光催化降解实验中表现出良好的稳定性,经过5次循环后降解效率保持在85%以上。同时,在实验研究的基础上阐明了Bi2Sn2O7/CeO2光催化剂的光催化机理。

Abstract

Bi2Sn2O7 nanoparticles are loaded onto CeO2 microspheres via hydrothermal method to produce Z-type heterojunction for photocatalytic degradation of contaminants in water.Results show that the degradation efficiency of tetracycline hydrochloride by the optimized Bi2Sn2O7/CeO2 (BSC-5) reaches 88.4% after 60 minutes of exposure to light (reaction rate constant k=0.0334 min-1),which is 8.25 times that over CeO2 and 4.71 times that over Bi2Sn2O7.Z-type heterojunction can form more exposed active centers,presenting better photoelectron-hole pair separation efficiency and excellent redox ability,and effectively generating superoxide radicals (·O-2) and hydroxyl radicals (·OH).In addition,Bi2Sn2O7/CeO2 shows good stability in photocatalytic degradation experiments,and delivers a degradation efficiency above 85% after 5 cycles.Meanwhile,the photocatalytic mechanism of Bi2Sn2O7/CeO2 photocatalyst is elucidated on the basis of experimental study.

关键词

Bi2Sn2O7/CeO2 / 四环素 / Z型异质结

Key words

Bi2Sn2O7/CeO2 / tetracycline / Z-type heterojunction

Author summay

王妮都(1999-),女,硕士生,研究方向为新能源材料的合成与应用,wangnidu@zjou.edu.cn;杨淑清(1974-),女,博士,副教授,研究方向为离子液体的催化应用以及轻质油品中硫化物的组成结构分析,通讯联系人,ysqjane@163.com。

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Bi2Sn2O7/CeO2Z型异质结光催化剂在可见光下降解有机污染物性能研究[J]. 现代化工, 2024, 44(3): 175-181 DOI:10.16606/j.cnki.issn0253-4320.2024.03.031

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