自愈水凝胶
材料科学
构造(python库)
纳米技术
共价键
动态共价化学
聚合物
可重用性
多样性(控制论)
复合材料
计算机科学
化学
高分子化学
分子
超分子化学
有机化学
人工智能
程序设计语言
软件
作者
Wei Wang,Yinyu Zhang,Wenguang Liu
标识
DOI:10.1016/j.progpolymsci.2017.04.001
摘要
In nature, many soft supporting tissues capable of withstanding multiform external forces during various activities consist of high strength hydrogels (HSHGs) in their delicately organized structures, in which non-covalent interactions play an irreplaceable role in the formation of these HSHGs systems. Inspired by this, researchers have attempted to develop many strategies to construct HSHGs by introducing dynamic and reversible non-covalent interactions in polymer networks. In the last decade, various non-covalent interactions were employed as the enhancing factors to produce a series of multifunctional HSHGs in our lab. By incorporating dynamic non-covalent interactions into hydrogel systems, a myriad of intriguing properties have been unraveled, such as fatigue resistance, self-healing, thermoresponsiveness and/or pH responsiveness, self-recovery, shape memory, and remoldability/recyclability/reusability, and their encouraging applications have been explored as well. However, achieving functionalized HSHGs and extending them to a broad range of applications is still in its infancy. This article provides an overview of bioinspired construction of HSHGs by utilizing a variety of non-covalent interactions; their applications in diverse fields are also presented. Meanwhile, we point out the future development of non-covalent interaction-reinforced HSHGs and potential challenges.
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