Zhu Chao Nan, Li Chen Yu, Wang Hu, Hong Wei, Huang Feihe, Zheng Qiang, Wu Zi Liang
Ministry of Education Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University, Hangzhou, 310027, China.
State Key Laboratory of Chemical Engineering, Center for Chemistry of High-Performance and Novel Materials, Department of Chemistry, Zhejiang University, Hangzhou, 310027, China.
Adv Mater. 2021 May;33(18):e2008057. doi: 10.1002/adma.202008057. Epub 2021 Mar 31.
Morphing hydrogels have versatile applications in soft robotics, flexible electronics, and biomedical devices. Controlling component distribution and internal stress within a hydrogel is crucial for shape-changing. However, existing gradient structures of hydrogels are usually non-reconstructable, once encoded by chemical reactions and covalent bonds. Fabricating hydrogels with distinct gradient structures is inevitable for every new configuration, resulting in poor reusability, adaptability, and sustainability that are disadvantageous for diverse applications. Herein, a hydrogel containing reversible photo-crosslinks that enable reprogramming of the gradient structures and 3D deformations into various configurations is reported. The hydrogel is prepared by micellar polymerization of hydrophobic coumarin monomer and hydrophilic acrylic acid. The presence of hexadecyltrimethylammonium chloride micelles increases the local concentration of coumarin units and also improves the mechanical properties of the hydrogel by forming robust polyelectrolyte/surfactant complexes that serve as the physical crosslinks. High-efficiency photodimerization and photocleavage reactions of coumarins are realized under 365 and 254 nm light irradiation, respectively, affording reversible tuning of the network structure of the hydrogel. Through photolithography, different gradient structures are sequentially patterned in one hydrogel that direct the deformations into distinct configurations. Such a strategy should be applicable for other photolabile hydrogels toward reprogrammable control of network structures and versatile functions.
变形水凝胶在软机器人技术、柔性电子学和生物医学设备中具有广泛的应用。控制水凝胶内的成分分布和内部应力对于形状改变至关重要。然而,水凝胶现有的梯度结构一旦由化学反应和共价键编码,通常是不可重构的。对于每一种新的构型,制造具有不同梯度结构的水凝胶是不可避免的,这导致了可重复使用性、适应性和可持续性较差,不利于各种应用。在此,报道了一种含有可逆光交联的水凝胶,其能够对梯度结构进行重新编程,并将3D变形转变为各种构型。该水凝胶通过疏水性香豆素单体和亲水性丙烯酸的胶束聚合制备。十六烷基三甲基氯化铵胶束的存在增加了香豆素单元的局部浓度,并且还通过形成作为物理交联的强大聚电解质/表面活性剂复合物来改善水凝胶的机械性能。香豆素分别在365和254nm光照射下实现了高效的光二聚化和光裂解反应,从而实现了水凝胶网络结构的可逆调节。通过光刻技术,在一种水凝胶中依次图案化不同的梯度结构,将变形引导成不同的构型。这种策略应该适用于其他对光不稳定的水凝胶,以实现对网络结构和多功能的可重新编程控制。