材料科学
执行机构
软机器人
刚度
超分子化学
仿生学
软质材料
超分子聚合物
聚合物
人工肌肉
计算机科学
构造(python库)
纳米技术
离子键合
机械工程
智能材料
变量(数学)
机制(生物学)
电活性聚合物
仿生材料
结构工程
气动执行机构
作者
Jiajie Jing,Bowen Yao,Wen Bin Sun,Jiaoyang Chen,Jian‐Hua Xu,Jiajun Fu
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-08-01
卷期号:63 (42): e202410693-e202410693
被引量:11
标识
DOI:10.1002/anie.202410693
摘要
Abstract 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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