Ma Yanfei, Hua Mutian, Wu Shuwang, Du Yingjie, Pei Xiaowei, Zhu Xinyuan, Zhou Feng, He Ximin
State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China.
Department of Material Science and Engineering, University of California Los Angeles, Los Angeles, CA 90095, USA.
Sci Adv. 2020 Nov 18;6(47). doi: 10.1126/sciadv.abd2520. Print 2020 Nov.
Stimuli-responsive hydrogels have large deformability but-when applied as actuators, smart switch, and artificial muscles-suffer from low work density due to low deliverable forces (2 kPa) and speed through the osmotic pressure-driven actuation. Inspired by the energy conversion mechanism of many creatures during jumping, we designed an elastic-driven strong contractile hydrogel through storing and releasing elastic potential energy in polymer network. It can generate high contractile force (40 kPa) rapidly at ultrahigh work density (15.3 kJ/m), outperforming current hydrogels (0.01 kJ/m) and even biological muscles (~8 kJ/m). This demonstrated elastic energy storing and releasing method endows hydrogels with elasticity-plasticity switchability, multi-stable deformability in fully reversible and programmable manners, and anisotropic or isotropic deformation. With the high power density and programmability via this customizable modular design, these hydrogels demonstrated potential for broad applications in artificial muscles, contractile wound dressing, and high-power actuators.
刺激响应水凝胶具有很大的可变形性,但在用作致动器、智能开关和人造肌肉时,由于渗透压驱动的致动产生的可传递力较低(约2千帕)且速度较慢,导致工作密度较低。受许多生物跳跃过程中能量转换机制的启发,我们通过在聚合物网络中存储和释放弹性势能,设计了一种弹性驱动的强收缩水凝胶。它可以在超高工作密度(15.3千焦/立方米)下快速产生高收缩力(40千帕),优于目前的水凝胶(约0.01千焦/立方米),甚至超过生物肌肉(约8千焦/立方米)。这种展示的弹性能量存储和释放方法赋予水凝胶弹性-塑性可切换性、以完全可逆和可编程方式的多稳态可变形性以及各向异性或各向同性变形。通过这种可定制的模块化设计,这些水凝胶具有高功率密度和可编程性,在人造肌肉、收缩性伤口敷料和高功率致动器等广泛应用中显示出潜力。