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Oxygen-vacancy-mediated photocatalytic degradation of tetracycline under weak visible-light irradiation over hierarchical Bi2MoO6@Bi2O3 core–shell fibers

机译:氧气介导介导的光催化降解四环素在弱的可见光照射下层次BI2MOO6@bi2O3核心核 - 壳纤维

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摘要

Novel oxygen-vacancy-rich hierarchical Bi2MoO6@Bi2O3 core–shell fibers were prepared by the in situ growth of Bi2MoO6 nanosheets on Bi2O3 nanofibers via an electrospinning–calcination–solvothermal method. The in situ growth contributed to the formation of an intimate interface between Bi2MoO6 nanosheets and Bi2O3 nanofibers, thereby constructing an efficient 1D/2D heterojunction and obtaining a 3D hierarchical structure at the same time. More importantly, the growth of Bi2MoO6 nanosheets on Bi2O3 yielded superficial oxygen vacancies. Such a special morphology and defect structure could not only increase the light harvesting, but also promote the separation of photo-induced electrons and holes through a Z-scheme charge transfer mechanism. Therefore, the Bi2MoO6@Bi2O3 composite photocatalyst showed excellent photocatalytic performance under weak visible-light illumination, thus exhibiting potential for application in the degradation of antibiotics. This promising Bi2MoO6@Bi2O3 photocatalyst had a superior photocatalytic degradation rate of 96.3% for TC under 5 W LED visible-light irradiation for 3 hours, which was 6.0 and 4.9 times higher than those of pristine Bi2O3 and Bi2MoO6, respectively. Moreover, two main possible photocatalytic degradation pathways for TC over the Bi2MoO6@Bi2O3 photocatalyst were also proposed.
机译:新型的氧气含量层次层次BI2MOO6@bi2O3核 - 壳纤维是通过通过静电纺丝 - 钙化 - 溶剂溶剂化方法在BI2MOO6纳米片上的原位生长来制备的。原位增长有助于BI2MOO6纳米片和Bi2O3纳米纤维之间形成紧密的接口,从而在同一时间构建有效的1D/2D异质结并获得3D层次结构。更重要的是,BI2MOO6纳米片在BI2O3上的生长产生了浅氧空位。这种特殊的形态和缺陷结构不仅可以增加光收集,而且还可以通过Z-Scheme电荷转移机制促进光诱导的电子和孔的分离。因此,在弱的可见光照明下,BI2MOO6@BI2O3复合光催化剂在弱的光照射下表现出极好的光催化性能,因此在抗生素降解中具有潜力。这种有希望的BI2MOO6@BI2O3光催化剂的光催化降解速率高于5 W LED LED LED可见光照射3小时的96.3%,分别是原始BI2O3和BI2MOO6的6.0倍和4.9倍。此外,还提出了TC在BI2MOO6@BI2O3光催化剂上的两个主要可能的光催化降解途径。

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