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具有协同效应的超薄h-BN/BiMoO异质结用于可见光光催化降解四环素

Ultrathin h-BN/BiMoO heterojunction with synergetic effect for visible-light photocatalytic tetracycline degradation.

作者信息

Du Zhao, Feng Lang, Guo Zhonglu, Yan Tongqi, Hu Qi, Lin Jing, Huang Yang, Tang Chengchun, Fang Yi

机构信息

School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130, China; Hebei Key Laboratory of Boron Nitride Micro and Nano Materials, Hebei University of Technology, Tianjin 300130, China.

School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130, China.

出版信息

J Colloid Interface Sci. 2021 May;589:545-555. doi: 10.1016/j.jcis.2021.01.027. Epub 2021 Jan 13.

Abstract

Herein, a series of ultrathin h-BN/BiMoO 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 BiMoO as well as the effective photogenerated carrier separation induced by the synergetic effect between h-BN and BiMoO. Moreover, DFT calculations reveal that the built-in electric field formed between h-BN and BiMoO 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/BiMoO heterojunction as a novel tetracycline degradation photocatalyst and further guides the design of more visible-light photocatalysts.

摘要

在此,通过一种可行的溶剂热法首次制备了一系列具有优异光催化活性的超薄h-BN/BiMoO异质结。我们的结果表明,优化后的光催化剂在可见光照射下对四环素(TC)、土霉素(OTC)和强力霉素(DC)的降解率分别高达99.19%、95.28%和91.04%。我们强调,出色的光催化活性主要归因于h-BN对四环素的显著吸附性能、BiMoO对可见光的主要吸收以及h-BN和BiMoO之间协同效应诱导的有效光生载流子分离。此外,密度泛函理论计算表明,h-BN和BiMoO之间形成的内建电场导致载流子分离和四环素分子的极化。最后但同样重要的是,还阐明了可见光驱动下光催化四环素降解的具体过程和微观机制。本工作开创了超薄h-BN/BiMoO异质结作为新型四环素降解光催化剂的应用,并进一步指导了更多可见光光催化剂的设计。

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