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原位构建碳酸氧铋/溴氧化铋Z型异质结用于高效光催化去除四环素和环丙沙星

In situ construction bismuth oxycarbonate/bismuth oxybromide Z-scheme heterojunction for efficient photocatalytic removal of tetracycline and ciprofloxacin.

作者信息

Yan Xuemei, Ji Qingjie, Wang Chao, Xu Jixiang, Wang Lei

机构信息

Key Laboratory of Eco-Chemical Engineering, Ministry of Education, State Laboratory of Inorganic Synthesis and Applied Chemistry, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.

Key Laboratory of Eco-Chemical Engineering, Ministry of Education, State Laboratory of Inorganic Synthesis and Applied Chemistry, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.

出版信息

J Colloid Interface Sci. 2021 Apr;587:820-830. doi: 10.1016/j.jcis.2020.11.043. Epub 2020 Nov 13.

Abstract

Finely engineering the morphology and regulating the hybrid interface of each component in a heterojunction are important for facilitating charge carrier separation. In this study, a flower-like bismuth oxycarbonate/bismuth oxybromide (BiOCO/BiOBr, BOC/BiOBr) Z-scheme heterojunction was prepared via generation of BOC followed by in situ self-growth of BiOBr on just generated BOC. The obtained photocatalyst has an interlaced nanosheet structure with oxygen vacancies, which enhances light adsorption and facilitates the migration and separation of charge carriers. The highest apparent rate constants (k) in the degradation of tetracycline and ciprofloxacin using the BOC/BiOBr-2 photocatalyst under visible-light irradiation were 0.0282 and 0.0220 min, respectively; these values were 6.1 and 6.2 times, respectively higher than that achieved using BOC as a photocatalyst. The hybrid mode of BOC and BiOBr, and the Z-scheme electron transfer path and oxygen vacancies present in BOC/BiOBr are the factors responsible for its high photocatalytic activity.

摘要

精细设计异质结中各组分的形貌并调控其杂化界面对于促进电荷载流子的分离至关重要。在本研究中,通过生成碱式碳酸铋(BOC),然后在刚生成的BOC上原位自生长溴氧化铋(BiOBr),制备了一种花状碱式碳酸铋/溴氧化铋(BiOCO/BiOBr,BOC/BiOBr)Z型异质结。所制备的光催化剂具有带氧空位的交错纳米片结构,这增强了光吸附并促进了电荷载流子的迁移和分离。在可见光照射下,使用BOC/BiOBr-2光催化剂降解四环素和环丙沙星时的最高表观速率常数(k)分别为0.0282和0.0220 min⁻¹;这些值分别比使用BOC作为光催化剂时高6.1倍和6.2倍。BOC与BiOBr的杂化模式以及BOC/BiOBr中存在的Z型电子转移路径和氧空位是其高光催化活性的原因。

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