Meng Zhi-Jun, Liu Ji, Yu Ziyi, Zhou Hantao, Deng Xu, Abell Chris, Scherman Oren A
Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu 610054, People's Republic of China.
Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, United Kingdom.
ACS Appl Mater Interfaces. 2020 Apr 15;12(15):17929-17935. doi: 10.1021/acsami.9b21240. Epub 2020 Mar 31.
Fiber-shaped soft constructs are indispensable building blocks for various 3D functional objects such as hierarchical structures within the human body. The design and fabrication of such hierarchically structured soft materials, however, are often challenged by the trade-offs between stiffness, toughness, and continuous production. Here, we describe a microfluidic platform to continuously fabricate double network hydrogel microfibers with tunable structural, chemical, and mechanical features. Construction of the double network microfibers is accomplished through the incorporation of dynamic cucurbit[]uril host-guest interactions, as energy dissipation moieties, within an agar-based brittle network. These microfibers exhibit an increase in fracture stress, stretchability, and toughness by 2-3 orders of magnitude compared to the pristine agar network, while simultaneously gaining recoverable hysteretic energy dissipation without sacrificing mechanical strength. This strategy of integrating a wide range of dynamic interactions with the breadth of natural resources could be used in the preparation of functional hydrogels, providing a versatile approach toward the continuous fabrication of soft materials with programmable functions.
纤维状软结构是各种三维功能物体(如人体内部的层次结构)不可或缺的构建块。然而,这种层次结构软材料的设计和制造常常受到刚度、韧性和连续生产之间权衡的挑战。在此,我们描述了一种微流控平台,用于连续制造具有可调结构、化学和机械特性的双网络水凝胶微纤维。双网络微纤维的构建是通过在基于琼脂的脆性网络中引入动态葫芦脲主客体相互作用作为能量耗散部分来实现的。与原始琼脂网络相比,这些微纤维的断裂应力、拉伸性和韧性提高了2 - 3个数量级,同时在不牺牲机械强度的情况下获得了可恢复的滞后能量耗散。这种将广泛的动态相互作用与丰富的自然资源相结合的策略可用于制备功能性水凝胶,为连续制造具有可编程功能的软材料提供了一种通用方法。