材料科学
执行机构
智能聚合物
聚合物
纳米技术
氢键
变形
仿生学
人工肌肉
智能材料
计算机科学
化学工程
高分子科学
复合材料
人工智能
分子
有机化学
工程类
化学
作者
Hao Hu,Mingzhe Nie,Massimiliano Galluzzi,Xue‐Feng Yu,Xuemin Du
标识
DOI:10.1002/adfm.202304634
摘要
Abstract Artificial intelligent actuators are extensively explored for emerging applications such as soft robots, human‐machine interfaces, and biomedical devices. However, intelligent actuating systems based on synthesized polymers suffer from challenges in renewability, sustainability, and safety, while natural polymer‐based actuators show limited capabilities and performances due to the presence of abundant hydrogen‐bond lockers. Here this study reports a new hydrogen bond‐mediated strategy to develop mimosa‐inspired starch actuators (SA). By harnessing the unique features of gelatinization and abundant hydrogen bonds, these SA enable high‐sensitivity and multi‐responsive actuation in various scenarios. The non‐gelatinized SA can be irreversibly programmed into diverse shapes, such as artificial flowers, bowl shapes, and helix structures, using near‐infrared light. Furthermore, the gelatinized SA exhibit reversibly multi‐responsive actuation when exposed to low humidity (10.2%), low temperature (37 °C), or low‐energy light (0.42 W cm −2 ). More importantly, the SA demonstrate robust applications in smart living, including artificial mimosa, intelligent lampshade, and morphing food. By overcoming the hydrogen‐bond lockers inherent in natural polymers, SA open new avenues for next‐generation recyclable materials and actuators, bringing them closer to practical applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI