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将少层 TiCT 嵌入碱化 g-CN 纳米片中以实现高效光催化降解。

Embedding few-layer TiCT into alkalized g-CN nanosheets for efficient photocatalytic degradation.

机构信息

State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan University, Changsha 410082, PR China.

College of Materials Science and Engineering, Hunan University, Changsha 410082, PR China.

出版信息

J Colloid Interface Sci. 2020 Jul 1;571:297-306. doi: 10.1016/j.jcis.2020.03.061. Epub 2020 Mar 17.

DOI:10.1016/j.jcis.2020.03.061
PMID:32208200
Abstract

Solution of the increasingly important problem of aquatic pollution requires the use of an economical, energy-efficient, highly effective and environmentally-friendly catalyst. Polymeric carbon nitride (CN) has shown to be a promising metal-free photocatalyst that however suffers from strong charge recombination and poor conductivity, while MXenes have shown to be perfect co-catalysts for the photocatalytic process but show poor stability. In this study, we successfully constructed a robust heterostructure photocatalyst in which few-layer TiCT was embedded into alkalized CN without being oxidized. The photocatalyst showed stable and effective photocatalytic performance for the removal of tetracycline hydrochloride and other organic compounds under visible light irradiation. Different characterization methods were used to elucidate the morphology and structure of the as-prepared photocatalyst. The robust heterostructure and the intimate interaction between the two constituents of the composite were verified. Based on the van der Waals heterostructure, TiCT acts as the electron acceptor and helps to form Schottky junction, preventing charge recombination of the photocatalyst. And in the meantime, the electrons from CN protect TiCT from oxidation. SEM and XRD results demonstrated that the TiCT structure remains unchanged after calcination and after photodegradation experiments. Furthermore, a possible mechanism for photocatalytic tetracycline hydrochloride degradation was proposed based on the results of radical scavenging experiments. This work provides a strategy to strengthen heterostructure between 2D materials, and shows that carbon nitride and Mxenes could be promising materials for photocatalytic wastewater pre-treatment applications.

摘要

解决日益严重的水污染问题需要使用经济、节能、高效且环保的催化剂。聚合碳氮化物(CN)已被证明是一种很有前途的无金属光催化剂,但它存在着强烈的电荷复合和较差的导电性问题,而 MXenes 则被证明是光催化过程的理想共催化剂,但它们的稳定性较差。在本研究中,我们成功地构建了一种稳健的异质结构光催化剂,其中将少层 TiCT 嵌入到未被氧化的碱化 CN 中。该光催化剂在可见光照射下表现出稳定而有效的光催化性能,可去除盐酸四环素和其他有机化合物。采用不同的表征方法对所制备的光催化剂的形貌和结构进行了阐明。证实了所制备的复合材料具有稳健的异质结构和两种组分之间的紧密相互作用。基于范德华异质结构,TiCT 作为电子受体,有助于形成肖特基结,防止光催化剂的电荷复合。同时,来自 CN 的电子保护 TiCT 免受氧化。SEM 和 XRD 结果表明,TiCT 结构在煅烧和光降解实验后保持不变。此外,根据自由基捕获实验的结果,提出了一种用于光催化盐酸四环素降解的可能机制。这项工作提供了一种增强二维材料之间异质结构的策略,并表明碳氮化物和 MXenes 可能是用于光催化废水预处理应用的有前途的材料。

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