自愈水凝胶
催化作用
过硫酸铵
材料科学
金属
化学工程
激进的
纳米技术
聚合
水溶液中的金属离子
氧化还原
高分子化学
化学
聚合物
复合材料
有机化学
冶金
工程类
作者
Zhanrong Jia,Yan Zeng,Pengfei Tang,Donglin Gan,Wensi Xing,Yue Hou,Kefeng Wang,Chaoming Xie,Xiong Lu
标识
DOI:10.1021/acs.chemmater.9b01498
摘要
Tough and conductive hydrogels are the promising materials for various applications. However, fabrication of these hydrogels at room or low temperatures, without external stimuli, is a challenge. Herein, a novel dual self-catalytic system composed of a variety of metal ions and catechol-based molecules was developed to efficiently trigger the free-radical polymerization of tough, conductive, transparent, and self-healing hydrogels at low temperature without any external stimuli. Ferric ions (Fe3+) and dopamine (DA) were chosen as model compounds, which form stable redox pairs that act as a dual self-catalytic system to activate ammonium persulfate to generate free radicals. Consequently, the radicals could rapidly trigger the hydrogel self-gelation at low temperatures (6 °C) within 5 s. The dual self-catalytic system opens up a facile route to synthesize multifunctional hydrogels at mild conditions for a broad range of applications, especially in tissue engineering and wearable electronics.
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