材料科学
制作
纳米技术
稳健性(进化)
聚合物
支化(高分子化学)
共聚物
复合材料
生物化学
医学
基因
病理
化学
替代医学
作者
Chuao Ma,Jun Wei,Yuqiang Zhang,Xingchao Chen,Чан Лю,Shen Diao,Yuan Gao,Krzysztof Matyjaszewski,Hongliang Liu
标识
DOI:10.1002/adfm.202211771
摘要
Abstract Currently, the increasing needs of conductive ionogels with intricate shapes and high processability by individual requirements of next‐generation flexible electronics constitute significant challenges. Here, the design of highly processable ionogels is reported with mechanical robustness by self‐assembly of a common triblock copolymer into a precursor in functional mixed ionic liquids (ILs) containing conductivity‐enhancing and polymerizable strength‐enhancing components. The subsequent in situ polymerization of the precursor forms physical‐co‐chemical cross‐linked networks, in which the entanglement between physical and chemical cross‐linked networks and microphase separation give rise to mechanical robustness of as‐fabricated ionogel. The viscosity of the self‐assembled precursor can be rationally tuned, which makes the fabrication process compatible with diverse technologies including inkjet printing, spray coating, and 3D printing. By virtue of highly processable capability of the designed ionogels, an auxetic‐structured ionogel can be easily generated using 3D printing, which exhibits greatly improved sensitivity and thus is able to monitor tiny deformations. This study that relies on designing functional mixed ILs as the dispersion phase rather than focusing on synthesizing new‐type polymers establishes a new route for versatile and programmable fabrication of high‐performance ionogels for broader applications.
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