降级(电信)
光催化
制作
异质结
聚苯乙烯
四环素
材料科学
化学工程
纳米技术
光电子学
化学
复合材料
计算机科学
有机化学
催化作用
电信
医学
工程类
聚合物
病理
替代医学
抗生素
生物化学
作者
Wensheng Zhang,Qingmei Tan,Tianren Liu,Ying He,Gang Chen,Ke Chen,Dongxue Han,Dongdong Qin,Li Niu
出处
期刊:Materials horizons
[Royal Society of Chemistry]
日期:2023-01-01
卷期号:10 (12): 5869-5880
被引量:28
摘要
The exploration of advanced photocatalysts for antibiotic degradation is critical, but it remains a challenge due to the lack of rational structural design and in-depth insights into molecular oxygen activation. Water-floating photocatalysts could be one of the best choices owing to their technical features in terms of reasonability and efficiency involving a high oxygenation of photocatalyst surface, fully solar irradiation, and simple recycling and reuse. Herein, a floatable litchi-like architecture of a polystyrene-sphere-supported TiO2/Bi2O3 (PS@TiO2/Bi2O3) S-scheme heterojunction was skillfully constructed and evaluated for photodegradation of model tetracycline (TC) antibiotics. By integrating the advantages of floatability and S-scheme, the TC removal rate of the optimal PS@TiO2/Bi2O3-0.4 catalyst can reach 88.4% under 1 h illumination, which is higher than that of pristine Bi2O3 (60.8%) and PS@TiO2 (40.1%). Moreover, PS@TiO2/Bi2O3-0.4 exhibits high recyclability and stability, and there is no significant loss of activity after five cycles of repeated use. With the aid of liquid chromatography-mass spectrometry analysis and density functional theory calculations, a reasonable degradation pathway for TC was proposed. The present work provides a recyclable and efficient approach for the photodegradation of TC, expecting to guide the innovative exploitation of other environmental systems.
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