材料科学
电致变色
自愈水凝胶
聚合物
韧性
超分子化学
纳米技术
化学工程
复合材料
分子
电极
高分子化学
化学
有机化学
工程类
物理化学
作者
Kaifang Wang,Hai Wang,Jingjing Li,Yujia Liang,Xiao‐Qiao Xie,Junpeng Liu,Chaonan Gu,Yunfei Zhang,Guo Zhang,Chun‐Sen Liu
出处
期刊:Materials horizons
[The Royal Society of Chemistry]
日期:2021-01-01
卷期号:8 (9): 2520-2532
被引量:80
摘要
The current tough and stretchable gels with various integrated functions are mainly based on polymer hydrogels. By introducing a non-covalent supramolecular self-assembled network into a covalently cross-linked polymer network in the presence of eco-friendly and cost-effective deep eutectic solvents (DESs), we developed a new small molecule-based supramolecular-polymer double-network (SP-DN) eutectogel platform. This exciting material exhibits high stretchability and toughness (>18 000% areal strain), spontaneous self-healing ability, ultrafast (∼5 s) in situ underwater and low-temperature (-80 °C) adhesion, and unusual boiling water-resistance, as well as strong base-, strong acid- (even aqua regia), ultra-low-temperature- (liquid nitrogen, -196 °C), and high-temperature- (200 °C) resistance. All these outstanding properties strongly recommend the SP-DN eutectogels as a quasi-solid electrolyte for soft electrochromic devices, which exhibited exceptional flexibility and consistent electrochromic behaviours in harsh mechanical or temperature environments. The experimental and simulation results uncovered the assembly mechanism of the SP-DN eutectogels. Unlike polymer hydrogels, the obtained SP-DN eutectogels showed high molecular design freedom and structural versatility. The findings of this work offer a promising strategy for developing the next generation of mechanically robust and functionally integrated soft materials with high environmental adaptability.
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