自愈水凝胶
仿生学
材料科学
共聚物
聚乙二醇
PEG比率
纳米技术
海参
聚合物
高分子化学
化学
复合材料
地质学
有机化学
经济
古生物学
财务
作者
Longyu Li,Qianming Lin,Miao Tang,Esther H. R. Tsai,Chenfeng Ke
标识
DOI:10.1002/ange.202017019
摘要
Abstract The development of integrated systems that mimic the multi‐stage stiffness change of marine animals such as the sea cucumber requires the design of molecularly tailored structures. Herein, we used an integrated biomimicry design to fabricate a sea cucumber mimic using sidechain polypseudorotaxanes with tunable nano‐to‐macroscale properties. A series of polyethylene glycol (PEG)‐based sidechain copolymers were synthesized to form sidechain polypseudorotaxanes with α‐cyclodextrins (α‐CDs). By tailoring the copolymers’ molecular weights and their PEG grafting densities, we rationally tuned the sizes of the formed polypseudorotaxanes crystalline domain and the physical crosslinking density of the hydrogels, which facilitated 3D printing and the mechanical adaptability to these hydrogels. After 3D printing and photo‐crosslinking, the obtained hydrogels exhibited large tensile strain and broad elastic‐to‐plastic variations upon α‐CD (de)threading. These discoveries enabled a successful fabrication of a sea cucumber mimic, demonstrating multi‐stage stiffness changes.
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