光催化
四环素
异质结
材料科学
光化学
可见光谱
降级(电信)
化学工程
盐酸四环素
光电子学
化学
催化作用
有机化学
工程类
电信
抗生素
生物化学
计算机科学
作者
Zhao Du,Lang Feng,Zhonglu Guo,Tongqi Yan,Qi Hu,Jing Lin,Yang Huang,Chengchun Tang,Yi Fang
标识
DOI:10.1016/j.jcis.2021.01.027
摘要
Herein, a series of ultrathin h-BN/Bi2MoO6 heterojunction with excellent photocatalytic activity has been firstly prepared via a feasible solvothermal method. Our results suggest that the optimized photocatalyst possesses a high degradation ratio of tetracycline (TC), oxytetracycline (OTC) and doxycycline (DC) up to 99.19%, 95.28% and 91.04% under visible-light irradiation, respectively. We highlight that the outstanding photocatalytic activity is mainly attributed to the prominent performance of tetracycline adsorption on h-BN and the dominant visible-light absorption by Bi2MoO6 as well as the effective photogenerated carrier separation induced by the synergetic effect between h-BN and Bi2MoO6. Moreover, DFT calculations reveal that the built-in electric field formed between h-BN and Bi2MoO6 gives rise to the separation of carriers and the polarization of tetracycline molecules. Last but not the least, the specific process and micro-mechanism of the photocatalytic tetracycline degradation under visible-light driven have also been illuminated. The present work pioneers the application of ultrathin h-BN/Bi2MoO6 heterojunction as a novel tetracycline degradation photocatalyst and further guides the design of more visible-light photocatalysts.
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