Covalent organic framework nanorods bearing single Cu sites for efficient photocatalysis

被引:107
|
作者
Dong, Zhiyue [1 ]
Zhang, Liang [2 ]
Gong, Jiang [1 ]
Zhao, Qiang [1 ]
机构
[1] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Hubei Key Lab Mat Chem & Serv Failure, Minist Educ,Sch Chem & Chem Engn, Wuhan 430074, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Minist Educ, Key Lab Biomed Polymers, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
Covalent organic framework; Nanostructure; Metallic atom; Photocatalysis; Sulfamethoxazole; Electrons-holes separation; HYDROGEN-PRODUCTION; DEGRADATION; CO2; PHOTODEGRADATION; HETEROJUNCTION; FABRICATION; WATER;
D O I
10.1016/j.cej.2020.126383
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Covalent organic frameworks (COFs) nanostructures capable of efficient visible light absorption, complete holes-electrons separation, and reactant enrichment remain a synthetic challenge for advanced photocatalysts. Herein, we rationally design a novel Cu-coordinated terpyridyl-based, 2D lamellar COF-909(Cu) nanorods. The coordinated single Cu sites not only dramatically enhance the visible light absorption and achieve the complete electrons-holes separation, but also provide the specific binding sites to enrich N/O-containing organic toxicants. The laminar arrangement and 1D nanochannel of COF-909(Cu) nanorods shorten the transfer distance of electrons to the active sites. As a proof of concept, it shows excellent performance in the photocatalytic degradation of sulfamethoxazole, which surpasses the-state-of-art photocatalysts. Density functional theory calculations confirm the structure-function relationship between the single Cu sites and the complete electrons-holes separation as well as strong binding sites for target molecules.
引用
收藏
页数:10
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