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通过尿素的均相超分子组装,氧掺杂石墨相氮化碳实现对抗生素污染物的高效可见光驱动降解。

Efficient visible light driven degradation of antibiotic pollutants by oxygen-doped graphitic carbon nitride via the homogeneous supramolecular assembly of urea.

作者信息

Cao Shihai, Zhang Yu, Ding Keqiang, Xu Jianhua, Zhao Yuqi, Wang Yi, Xie Xianchuan, Wang Huiya

机构信息

College of Environmental Engineering, Nanjing Institute of Technology, Nanjing, 211167, China.

Key Laboratory of Jiangsu Province for Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China.

出版信息

Environ Res. 2022 Jul;210:112920. doi: 10.1016/j.envres.2022.112920. Epub 2022 Feb 12.

Abstract

Graphitic carbon nitride (CN), as a non-metal material, has emerged as a promising photocatalyst to address environmental issues with the favorable band gap and chemical stability. The porous oxygen-doped CN nanosheets (CNO) were synthesized by an ecofriendly and efficient self-assembled approach using a sole urea as the precursor. The CNO photocatalysts were derived from the hydrogen-bonded cyanuric acid-urea supramolecular complex, which were obtained by pretreatment of urea at high temperature and pressure. The homogeneous supramolecular assembly was advantageous to the formation of uniform porous and oxygen-doped CN nanosheets. The formation process of the supramolecular intermediate and the CNO nanosheets were investigated. Moreover, doping amount of O in CNO could be controlled by the time of the high-pressure thermal polymerization of urea. The characterization results shown that the O atoms were successfully doped into the framework of CN by substitution the N atoms to form the C-O structures. The obtained CNO photocatalysts demonstrated the excellent visible-light photocatalytic performances for sulfamerazine (SMR) degradation, which was ascribed to synergistic interaction of porous structure and O doping. The degradation intermediates of SMR were identified and the degradation pathway were also proposed. Furthermore, density functional theory (DFT) calculations proved that O doping changed the electronic structure of CN, resulting in more easier to activate O. This work provides a novel perceptive for the development of high-performance nonmetal photocatalysts by using the homogeneous supramolecular assembly, which exhibits great potential in the environmental treatment.

摘要

石墨相氮化碳(CN)作为一种非金属材料,因其具有合适的带隙和化学稳定性,已成为一种有前景的光催化剂,可用于解决环境问题。采用环保高效的自组装方法,以单一尿素为前驱体,合成了多孔氧掺杂的CN纳米片(CNO)。CNO光催化剂源自氢键连接的氰尿酸 - 尿素超分子复合物,该复合物通过尿素在高温高压下的预处理获得。均匀的超分子组装有利于形成均匀的多孔且氧掺杂的CN纳米片。研究了超分子中间体和CNO纳米片的形成过程。此外,CNO中O的掺杂量可通过尿素高压热聚合的时间来控制。表征结果表明,O原子通过取代N原子成功掺杂到CN的骨架中,形成了C - O结构。所制备的CNO光催化剂对磺胺甲嘧啶(SMR)降解表现出优异的可见光光催化性能,这归因于多孔结构和O掺杂的协同作用。鉴定了SMR的降解中间体,并提出了降解途径。此外,密度泛函理论(DFT)计算证明,O掺杂改变了CN的电子结构,使得更容易活化O。这项工作为通过使用均匀超分子组装开发高性能非金属光催化剂提供了新的视角,在环境处理方面具有巨大潜力。

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