弹性体
自愈
材料科学
导电体
复合材料
共聚物
可伸缩电子设备
深共晶溶剂
单体
纳米技术
高分子化学
数码产品
聚合物
共晶体系
化学
替代医学
物理化学
合金
病理
医学
作者
Ren’ai Li,Ting Fan,Guangxue Chen,Kaili Zhang,Bin Su,Junfei Tian,Minghui He
标识
DOI:10.1021/acs.chemmater.9b04592
摘要
It is a challenge to synthesize all-in-one molecular networks that are autonomously self-healable over a wide temperature range (from subzero to high), transparent, stretchable, and conductive. Here we demonstrate the fabrication of self-healing, transparent, conductive, and highly stretchable elastomers by a photoinitiated copolymerization of two polymerizable deep eutectic solvent (PDES) monomers, acrylic amide (AAm)/choline chloride (ChCl) and maleic acid (MA)/ChCl type PDESs. Hydrogen bonds between binary building blocks of the poly(AAm/ChCl-co-MA/ChCl) system can readily break and reform, allowing such all organic designed elastomers to self-heal over a wide temperature ranging from −23 to 60 °C while keep a highly transparent appearance. The hypermolecular network elastomers showed a fast self-healing property (within 2 s) without any other external stimuli and excellent self-healing efficiency (up to 94%). The elastomers were highly transparent (an average transmittance of 95.1%), intrinsically conductive (an ionic conductivity of 4.0 × 10–4 S cm–1), and stretchable (strains up to 450%) at room temperature. We hypothesize that this behavior will find their potential use in display and/or optically related fields of stretchable electronics in harsh environments.
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