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Ultra-fast single-crystal polymerization of large-sized covalent organic frameworks
In principle, polymerization tends to produce amorphous or poorly crystalline materials. Efficiently producing high-quality single crystals by polymerization in solvent remains as an unsolved issue in chemistry, especially for covalent organic frameworks (COFs) with highly complex structures. To pro...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382702/ https://www.ncbi.nlm.nih.gov/pubmed/34426571 http://dx.doi.org/10.1038/s41467-021-24842-x |
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author | Peng, Lan Guo, Qianying Song, Chaoyu Ghosh, Samrat Xu, Huoshu Wang, Liqian Hu, Dongdong Shi, Lei Zhao, Ling Li, Qiaowei Sakurai, Tsuneaki Yan, Hugen Seki, Shu Liu, Yunqi Wei, Dacheng |
author_facet | Peng, Lan Guo, Qianying Song, Chaoyu Ghosh, Samrat Xu, Huoshu Wang, Liqian Hu, Dongdong Shi, Lei Zhao, Ling Li, Qiaowei Sakurai, Tsuneaki Yan, Hugen Seki, Shu Liu, Yunqi Wei, Dacheng |
author_sort | Peng, Lan |
collection | PubMed |
description | In principle, polymerization tends to produce amorphous or poorly crystalline materials. Efficiently producing high-quality single crystals by polymerization in solvent remains as an unsolved issue in chemistry, especially for covalent organic frameworks (COFs) with highly complex structures. To produce μm-sized single crystals, the growth time is prolonged to >15 days, far away from the requirements in practical applications. Here, we find supercritical CO(2) (sc-CO(2)) accelerates single-crystal polymerization by 10,000,000 folds, and produces two-dimensional (2D) COF single crystals with size up to 0.2 mm within 2~5 min. Although it is the fastest single-crystal polymerization, the growth in sc-CO(2) leads to not only the largest crystal size of 2D COFs, but also higher quality with improved photoconductivity performance. This work overcomes traditional concept on low efficiency of single-crystal polymerization, and holds great promise for future applications owing to its efficiency, industrial compatibility, environmental friendliness and universality for different crystalline structures and linkage bonds. |
format | Online Article Text |
id | pubmed-8382702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83827022021-09-22 Ultra-fast single-crystal polymerization of large-sized covalent organic frameworks Peng, Lan Guo, Qianying Song, Chaoyu Ghosh, Samrat Xu, Huoshu Wang, Liqian Hu, Dongdong Shi, Lei Zhao, Ling Li, Qiaowei Sakurai, Tsuneaki Yan, Hugen Seki, Shu Liu, Yunqi Wei, Dacheng Nat Commun Article In principle, polymerization tends to produce amorphous or poorly crystalline materials. Efficiently producing high-quality single crystals by polymerization in solvent remains as an unsolved issue in chemistry, especially for covalent organic frameworks (COFs) with highly complex structures. To produce μm-sized single crystals, the growth time is prolonged to >15 days, far away from the requirements in practical applications. Here, we find supercritical CO(2) (sc-CO(2)) accelerates single-crystal polymerization by 10,000,000 folds, and produces two-dimensional (2D) COF single crystals with size up to 0.2 mm within 2~5 min. Although it is the fastest single-crystal polymerization, the growth in sc-CO(2) leads to not only the largest crystal size of 2D COFs, but also higher quality with improved photoconductivity performance. This work overcomes traditional concept on low efficiency of single-crystal polymerization, and holds great promise for future applications owing to its efficiency, industrial compatibility, environmental friendliness and universality for different crystalline structures and linkage bonds. Nature Publishing Group UK 2021-08-23 /pmc/articles/PMC8382702/ /pubmed/34426571 http://dx.doi.org/10.1038/s41467-021-24842-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Peng, Lan Guo, Qianying Song, Chaoyu Ghosh, Samrat Xu, Huoshu Wang, Liqian Hu, Dongdong Shi, Lei Zhao, Ling Li, Qiaowei Sakurai, Tsuneaki Yan, Hugen Seki, Shu Liu, Yunqi Wei, Dacheng Ultra-fast single-crystal polymerization of large-sized covalent organic frameworks |
title | Ultra-fast single-crystal polymerization of large-sized covalent organic frameworks |
title_full | Ultra-fast single-crystal polymerization of large-sized covalent organic frameworks |
title_fullStr | Ultra-fast single-crystal polymerization of large-sized covalent organic frameworks |
title_full_unstemmed | Ultra-fast single-crystal polymerization of large-sized covalent organic frameworks |
title_short | Ultra-fast single-crystal polymerization of large-sized covalent organic frameworks |
title_sort | ultra-fast single-crystal polymerization of large-sized covalent organic frameworks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382702/ https://www.ncbi.nlm.nih.gov/pubmed/34426571 http://dx.doi.org/10.1038/s41467-021-24842-x |
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