弹性体
材料科学
自愈
极限抗拉强度
复合材料
氢键
超分子化学
金刚烷
聚合物网络
聚合物
高分子科学
分子
有机化学
病理
化学
替代医学
医学
作者
Junbo Hou,Xiaoqin Zhang,Di Wu,Junfeng Feng,Duo Ke,Bang‐Jing Li,Sheng Zhang
标识
DOI:10.1021/acsami.9b00626
摘要
Inspired by animal muscles, we developed a kind of tough elastomers combining high strength and high stretchability with autonomous self-healing capability. A key structural feature is the construction of a double network (DN) connected by the hydrogen bond and host-guest interactions. The first network is the classic elastomer polyacrylate matrix cross-linked by strong hydrogen bonding. The second network is formed through the host-guest interactions between polycyclodextrin and the adamantane (Ad) groups on the side of the polyacrylate chain. Supramolecular interactions between two networks make them miscible and interpenetrate in the molecular level and then can share the load as the sample was stretched. The host-guest interactions act not only as sacrificial bonds for energy dissipation but also as self-healing driving forces. The tensile strength of the DN elastomer reaches about 6.7 MPa and the strain is as high as about 950%. The DN elastomer can be easy to repair by touching the damaged surface together at ambient conditions when broken or cut. The recovered tensile strength can reach over 4.5 MPa, which is better than the most pristine strength of existing spontaneous self-healing elastomers.
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