韧性
材料科学
执行机构
超分子化学
刚度
软机器人
仿生学
聚合物
稳健性(进化)
超分子聚合物
纳米技术
软质材料
复合材料
计算机科学
机械工程
人工智能
分子
工程类
化学
有机化学
生物化学
基因
作者
Jiajie Jing,Bowen Yao,Wen Sun,Jiaoyang Chen,Jian‐Hua Xu,Jiajun Fu
标识
DOI:10.1002/ange.202410693
摘要
Variable stiffness materials have shown considerable application in soft robotics. However, previously reported materials often struggle to reconcile high stiffness, stretchability, toughness, and self‐healing ability, because of the inherently conflicting requisite of these properties in molecular design. Herein, we propose a novel strategy that involves incorporating acid‐base ionic pairs capable of from strong crosslinking sites into a dense and robust hydrogen‐bonding network to construct rigid self‐healing polymers with tunable stiffness and excellent toughness. To demonstrate these distinct features, the polymer was employed to serve as the strain‐regulation layers within a fiber‐reinforced pneumatic actuator (FPA). The exceptional synergy between the configuration versatility of FPA and the dynamic molecular behavior of the supramolecular polymers equips the actuator with simultaneous improvement in motion dexterity, multimodality, loading capacity, robustness, and durability. Additionally, the concept of integrating high dexterity at both macro‐ and micro‐scale is prospective to inspire the design of intelligent yet robust devices across various domains.
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