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Stimuli-responsive supramolecular hydrogels with high extensibility and fast self-healing via precoordinated mussel-inspired chemistry

机译:刺激响应的超分子水凝胶具有高可扩展性并通过预先配位的贻贝启发化学快速自我修复

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摘要

Supramolecular hydrogels have the advantages of stimuli responsiveness and self-healing compared to covalently crosslinked hydrogels. However, the existing supramolecular hydrogels are usually poor in mechanical properties especially in extensibility. In addition, these supramolecular hydrogels need a long self-healing time and have low self-healing efficiency. In this manuscript, we report a novel strategy to develop highly extensible and fast self-healing supramolecular hydrogels by using pre-coordinated mussel-inspired catechol-Fe3+ complexes as dynamic crosslinkers. The hydrogel can be fabricated and cast into various shapes by one-step photo-crosslinking. Thus fabricated hydrogels can be stretched beyond 10 times their original lengths, and the high extensibility can completely recover within a very short time (less than 20 minutes) even after the hydrogels are entirely cut apart. Utilizing the dynamic nature of supramolecular hydrogels, we can realize different mechanical behaviors including strength, extensibility and recoverability by varying the loading conditions. In addition, the hydrogels respond to multiple stimuli including mechanical force, temperature and certain chemicals because of the dynamic catechol-Fe3+ bond.
机译:与共价交联的水凝胶相比,超分子水凝胶具有刺激响应性和自我修复的优势。但是,现有的超分子水凝胶通常在机械性能,特别是延展性方面较差。另外,这些超分子水凝胶需要较长的自修复时间,并且自修复效率低。在本手稿中,我们报告了一种新策略,该策略通过使用预先配位的贻贝启发的邻苯二酚-Fe 3 + 复合物作为动态交联剂来开发高度可扩展且快速自修复的超分子水凝胶。水凝胶可以通过一步光致交联制备并浇铸成各种形状。这样制成的水凝胶可以被拉伸超过其原始长度的十倍,并且即使在将水凝胶完全切开之后,高可延展性也可以在很短的时间内(不到20分钟)完全恢复。利用超分子水凝胶的动力学性质,我们可以通过改变加载条件来实现不同的机械行为,包括强度,可扩展性和可恢复性。此外,由于动态的儿茶酚-Fe 3 + 键,水凝胶对多种刺激产生响应,包括机械力,温度和某些化学物质。

著录项

  • 期刊名称 other
  • 作者

    Sen Hou; Peter X. Ma;

  • 作者单位
  • 年(卷),期 -1(27),22
  • 年度 -1
  • 页码 7627–7635
  • 总页数 20
  • 原文格式 PDF
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