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A versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction
Hydrogen bond engineering is widely exploited to impart stretchability, toughness, and self-healing capability to hydrogels. However, the enhancement effect of conventional hydrogen bonds is severely limited by their weak interaction strength. In nature, some organisms tolerate extreme conditions du...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865770/ https://www.ncbi.nlm.nih.gov/pubmed/35196089 http://dx.doi.org/10.1126/sciadv.abl5066 |
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author | Han, Zilong Wang, Peng Lu, Yuchen Jia, Zheng Qu, Shaoxing Yang, Wei |
author_facet | Han, Zilong Wang, Peng Lu, Yuchen Jia, Zheng Qu, Shaoxing Yang, Wei |
author_sort | Han, Zilong |
collection | PubMed |
description | Hydrogen bond engineering is widely exploited to impart stretchability, toughness, and self-healing capability to hydrogels. However, the enhancement effect of conventional hydrogen bonds is severely limited by their weak interaction strength. In nature, some organisms tolerate extreme conditions due to the strong hydrogen bond interactions induced by trehalose. Here, we report a trehalose network–repairing strategy achieved by the covalent-like hydrogen bonding interactions to improve the hydrogels’ mechanical properties while simultaneously enabling them to tolerate extreme environmental conditions and retain synthetic simplicity, which proves to be useful for various kinds of hydrogels. The mechanical properties of trehalose-modified hydrogels including strength, stretchability, and fracture toughness are substantially enhanced under a wide range of temperatures. After dehydration, the modified hydrogels maintain their hyperelasticity and functions, while the unmodified hydrogels collapse. This strategy provides a versatile methodology for synthesizing extremotolerant, highly stretchable, and tough hydrogels, which expand their potential applications to various conditions. |
format | Online Article Text |
id | pubmed-8865770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-88657702022-03-10 A versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction Han, Zilong Wang, Peng Lu, Yuchen Jia, Zheng Qu, Shaoxing Yang, Wei Sci Adv Physical and Materials Sciences Hydrogen bond engineering is widely exploited to impart stretchability, toughness, and self-healing capability to hydrogels. However, the enhancement effect of conventional hydrogen bonds is severely limited by their weak interaction strength. In nature, some organisms tolerate extreme conditions due to the strong hydrogen bond interactions induced by trehalose. Here, we report a trehalose network–repairing strategy achieved by the covalent-like hydrogen bonding interactions to improve the hydrogels’ mechanical properties while simultaneously enabling them to tolerate extreme environmental conditions and retain synthetic simplicity, which proves to be useful for various kinds of hydrogels. The mechanical properties of trehalose-modified hydrogels including strength, stretchability, and fracture toughness are substantially enhanced under a wide range of temperatures. After dehydration, the modified hydrogels maintain their hyperelasticity and functions, while the unmodified hydrogels collapse. This strategy provides a versatile methodology for synthesizing extremotolerant, highly stretchable, and tough hydrogels, which expand their potential applications to various conditions. American Association for the Advancement of Science 2022-02-23 /pmc/articles/PMC8865770/ /pubmed/35196089 http://dx.doi.org/10.1126/sciadv.abl5066 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Physical and Materials Sciences Han, Zilong Wang, Peng Lu, Yuchen Jia, Zheng Qu, Shaoxing Yang, Wei A versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction |
title | A versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction |
title_full | A versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction |
title_fullStr | A versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction |
title_full_unstemmed | A versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction |
title_short | A versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction |
title_sort | versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction |
topic | Physical and Materials Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8865770/ https://www.ncbi.nlm.nih.gov/pubmed/35196089 http://dx.doi.org/10.1126/sciadv.abl5066 |
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