A versatile hydrogel network–repairing strategy achieved by the covalent-like hydrogen bond interaction

韧性 共价键 海藻糖 化学 纳米技术 氢键 自愈水凝胶 化学工程 材料科学 分子 复合材料 高分子化学 有机化学 工程类
作者
Zilong Han,Peng Wang,Yuchen Lu,Zheng Jia,Shaoxing Qu,Wei Yang
出处
期刊:Science Advances [American Association for the Advancement of Science]
卷期号:8 (8) 被引量:169
标识
DOI:10.1126/sciadv.abl5066
摘要

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.
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