Cao Feng, Wang Jianmin, Wang Yunan, Zhou Jun, Li Song, Qin Gaowu, Fan Weiqiang
Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), School of Material Science and Engineering, Northeastern University Shenyang 110819 China
School of Chemistry & Chemical Engineering, Jiangsu University Zhenjiang 212013 China
Nanoscale Adv. 2018 Dec 12;1(3):1124-1129. doi: 10.1039/c8na00197a. eCollection 2019 Mar 12.
Currently, there is an urgent demand for developing new materials to remove antibiotics in the water environment, especially for the simultaneous degradation of multiple antibiotics. Here, we fabricated a novel Bi/BiOBr heterostructure an solvothermal strategy, and it exhibited excellent visible-light-responsive photocatalytic activity for synchronously removing multiple antibiotics coexisting in water. The Bi nanoparticles could extend the light absorption spectra of the sample and further facilitate electron-hole pair separation. The in-depth electron spin resonance (ESR) results confirm that the active species in Bi/BiOBr are holes (h) and superoxide radicals (·O ) under irradiation, and it is also proved that Bi could selectively reduce the formation of ·O in the BiOBr matrix. The coexisting system of TC (tetracycline hydrochloride), CIP (ciprofloxacin) and DOX (doxycycline) could be simultaneously photodegraded to approximately 0% within 30 min by the Bi/BiOBr photocatalyst.
目前,迫切需要开发新型材料来去除水环境中的抗生素,特别是用于同时降解多种抗生素。在此,我们通过溶剂热法制备了一种新型的Bi/BiOBr异质结构,它对同步去除水中共存的多种抗生素表现出优异的可见光响应光催化活性。Bi纳米颗粒可以扩展样品的光吸收光谱,并进一步促进电子-空穴对的分离。深入的电子自旋共振(ESR)结果证实,Bi/BiOBr在光照下的活性物种是空穴(h)和超氧自由基(·O ),并且还证明Bi可以选择性地减少BiOBr基质中·O 的形成。Bi/BiOBr光催化剂可以在30分钟内将TC(盐酸四环素)、CIP(环丙沙星)和DOX(强力霉素)的共存体系同时光降解至约0%。