Covalent organic framework nanorods bearing single Cu sites for efficient photocatalysis
[Display omitted] •COF-909(Cu) nanorods based on a terpyridyl N-doped linker are facilely prepared.•COF-909(Cu) shows an improved visible light absorption due to single Cu sites.•The complete electron-hole separation in COF-909(Cu) is proved by DFT stimulation.•COF-909(Cu) enriches N/O-containing ta...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2021-01, Vol.403, p.126383, Article 126383 |
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Sprache: | eng |
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•COF-909(Cu) nanorods based on a terpyridyl N-doped linker are facilely prepared.•COF-909(Cu) shows an improved visible light absorption due to single Cu sites.•The complete electron-hole separation in COF-909(Cu) is proved by DFT stimulation.•COF-909(Cu) enriches N/O-containing target molecules by specific binding sites.•COF-909(Cu) exhibits high performance in photodegradation of sulfamethoxazole.
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. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2020.126383 |