自愈水凝胶
执行机构
聚电解质
调制(音乐)
化学
空间调制
材料科学
纳米技术
高分子化学
复合材料
物理
计算机科学
工程类
聚合物
电信
电气工程
声学
频道(广播)
多输入多输出
作者
Jinghua Duan,Wenxin Fan,Zihan Xu,Lu Cui,Ziyou Wang,Zhihong Nie,Kunyan Sui
标识
DOI:10.1002/ange.202410383
摘要
Hydrogel actuators with complex 3D initial shapes show numerous important applications, but it remains challenging to fabricate such actuators. This article describes a polyelectrolyte‐based strategy for modulating small‐scale internal stresses within hydrogels to construct complex actuators with tailored 3D initial shapes. Introducing polyelectrolytes into precursor solutions significantly enhances the volume shrinkage of hydrogel networks during polymerization, allowing us to modulate internal stresses. Photopolymerization of these polyelectrolyte‐containing solutions through a mask produces mechanically strong hydrogel sheets with large patterned internal stresses. Consequently, these hydrogel sheets attain complex 3D initial shapes at equilibrium, in contrast to the planar initial configuration of 2D actuators. We demonstrate that these 3D actuators can reversibly transform into other 3D shapes (i.e., 3D‐to‐3D shape transformations) in response to external stimuli. Additionally, we develop a predictive model based on the Flory‐Rehner theory to analyze the polyelectrolyte‐mediated shrinking behaviors of hydrogel networks during polymerization, allowing precise modulation of shrinkage and internal stress. This polyelectrolyte‐boosted shrinking mechanism paves a route to the fabrication of high‐performance 3D hydrogel actuators.
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