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Strongly Reducing (Diarylamino)benzene-Based Covalent Organic Framework for Metal-Free Visible Light Photocatalytic H(2)O(2) Generation
[Image: see text] Photocatalytic reduction of molecular oxygen is a promising route toward sustainable production of hydrogen peroxide (H(2)O(2)). This challenging process requires photoactive semiconductors enabling solar energy driven generation and separation of electrons and holes with high char...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705891/ https://www.ncbi.nlm.nih.gov/pubmed/33185433 http://dx.doi.org/10.1021/jacs.0c09684 |
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author | Krishnaraj, Chidharth Sekhar Jena, Himanshu Bourda, Laurens Laemont, Andreas Pachfule, Pradip Roeser, Jérôme Chandran, C. Vinod Borgmans, Sander Rogge, Sven M. J. Leus, Karen Stevens, Christian V. Martens, Johan A. Van Speybroeck, Veronique Breynaert, Eric Thomas, Arne Van Der Voort, Pascal |
author_facet | Krishnaraj, Chidharth Sekhar Jena, Himanshu Bourda, Laurens Laemont, Andreas Pachfule, Pradip Roeser, Jérôme Chandran, C. Vinod Borgmans, Sander Rogge, Sven M. J. Leus, Karen Stevens, Christian V. Martens, Johan A. Van Speybroeck, Veronique Breynaert, Eric Thomas, Arne Van Der Voort, Pascal |
author_sort | Krishnaraj, Chidharth |
collection | PubMed |
description | [Image: see text] Photocatalytic reduction of molecular oxygen is a promising route toward sustainable production of hydrogen peroxide (H(2)O(2)). This challenging process requires photoactive semiconductors enabling solar energy driven generation and separation of electrons and holes with high charge transfer kinetics. Covalent organic frameworks (COFs) are an emerging class of photoactive semiconductors, tunable at a molecular level for high charge carrier generation and transfer. Herein, we report two newly designed two-dimensional COFs based on a (diarylamino)benzene linker that form a Kagome (kgm) lattice and show strong visible light absorption. Their high crystallinity and large surface areas (up to 1165 m(2)·g(–1)) allow efficient charge transfer and diffusion. The diarylamine (donor) unit promotes strong reduction properties, enabling these COFs to efficiently reduce oxygen to form H(2)O(2). Overall, the use of a metal-free, recyclable photocatalytic system allows efficient photocatalytic solar transformations. |
format | Online Article Text |
id | pubmed-7705891 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-77058912020-12-02 Strongly Reducing (Diarylamino)benzene-Based Covalent Organic Framework for Metal-Free Visible Light Photocatalytic H(2)O(2) Generation Krishnaraj, Chidharth Sekhar Jena, Himanshu Bourda, Laurens Laemont, Andreas Pachfule, Pradip Roeser, Jérôme Chandran, C. Vinod Borgmans, Sander Rogge, Sven M. J. Leus, Karen Stevens, Christian V. Martens, Johan A. Van Speybroeck, Veronique Breynaert, Eric Thomas, Arne Van Der Voort, Pascal J Am Chem Soc [Image: see text] Photocatalytic reduction of molecular oxygen is a promising route toward sustainable production of hydrogen peroxide (H(2)O(2)). This challenging process requires photoactive semiconductors enabling solar energy driven generation and separation of electrons and holes with high charge transfer kinetics. Covalent organic frameworks (COFs) are an emerging class of photoactive semiconductors, tunable at a molecular level for high charge carrier generation and transfer. Herein, we report two newly designed two-dimensional COFs based on a (diarylamino)benzene linker that form a Kagome (kgm) lattice and show strong visible light absorption. Their high crystallinity and large surface areas (up to 1165 m(2)·g(–1)) allow efficient charge transfer and diffusion. The diarylamine (donor) unit promotes strong reduction properties, enabling these COFs to efficiently reduce oxygen to form H(2)O(2). Overall, the use of a metal-free, recyclable photocatalytic system allows efficient photocatalytic solar transformations. American Chemical Society 2020-11-13 2020-11-25 /pmc/articles/PMC7705891/ /pubmed/33185433 http://dx.doi.org/10.1021/jacs.0c09684 Text en © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Krishnaraj, Chidharth Sekhar Jena, Himanshu Bourda, Laurens Laemont, Andreas Pachfule, Pradip Roeser, Jérôme Chandran, C. Vinod Borgmans, Sander Rogge, Sven M. J. Leus, Karen Stevens, Christian V. Martens, Johan A. Van Speybroeck, Veronique Breynaert, Eric Thomas, Arne Van Der Voort, Pascal Strongly Reducing (Diarylamino)benzene-Based Covalent Organic Framework for Metal-Free Visible Light Photocatalytic H(2)O(2) Generation |
title | Strongly
Reducing (Diarylamino)benzene-Based Covalent
Organic Framework for Metal-Free Visible Light Photocatalytic H(2)O(2) Generation |
title_full | Strongly
Reducing (Diarylamino)benzene-Based Covalent
Organic Framework for Metal-Free Visible Light Photocatalytic H(2)O(2) Generation |
title_fullStr | Strongly
Reducing (Diarylamino)benzene-Based Covalent
Organic Framework for Metal-Free Visible Light Photocatalytic H(2)O(2) Generation |
title_full_unstemmed | Strongly
Reducing (Diarylamino)benzene-Based Covalent
Organic Framework for Metal-Free Visible Light Photocatalytic H(2)O(2) Generation |
title_short | Strongly
Reducing (Diarylamino)benzene-Based Covalent
Organic Framework for Metal-Free Visible Light Photocatalytic H(2)O(2) Generation |
title_sort | strongly
reducing (diarylamino)benzene-based covalent
organic framework for metal-free visible light photocatalytic h(2)o(2) generation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7705891/ https://www.ncbi.nlm.nih.gov/pubmed/33185433 http://dx.doi.org/10.1021/jacs.0c09684 |
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