Development of an Ionic Conductive Elastomer from the Photocopolymerization of a Ternary Polymerizable Deep Eutectic Solvent for Human Motions Sensing.

IF 4.2 3区 化学 Q2 POLYMER SCIENCE Macromolecular Rapid Communications Pub Date : 2024-11-15 DOI:10.1002/marc.202400798
Zhengyang Qian, Chenlin Pan, Hao Chen, Mingzu Zhang, Jinlin He, Peihong Ni
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Abstract

Polymerizable deep eutectic solvents (PDES) represent a novel class of ionic liquids characterized by the presence of polymerizable groups in their hydrogen-bond donor or acceptor components. Within the realm of flexible electronics, PDES is emerged as a promising material for the fabrication of sensors that exhibit both flexibility and stretchability. This research employs the UV-initiated photocopolymerization of a ternary PDES composed of choline chloride (ChCl), 2-hydroxyethyl acrylate (HEA), and itaconic acid (IA), to synthesize an ionic conductive elastomer (ICE) that boasts desirable comprehensive performances, which can be controlled by meticulously adjusting the ratios of these components. The fabrication process is streamlined and efficient, utilizing cost-effective and eco-friendly materials. This elastomer exhibits favorable ionic conductivity (1.70 × 10-2-5.45 × 10-2 S m-1), mechanical strength (0.48-1.21 MPa stress at break, 395-701% elongation at break), adhesion capacity (49-120 kPa adhesion strength), and sensing sensitivity toward human motions.

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利用三元可聚合深共晶溶剂的光聚合作用开发用于人体运动传感的离子导电弹性体
可聚合深共晶溶剂(PDES)是一类新型离子液体,其特点是在氢键供体或受体成分中存在可聚合基团。在柔性电子领域,PDES 已成为一种很有前途的材料,可用于制造具有柔性和拉伸性的传感器。本研究利用紫外线引发的光聚合反应,将氯化胆碱(ChCl)、丙烯酸羟乙酯(HEA)和衣康酸(IA)组成的三元 PDES 合成出一种离子导电弹性体(ICE),该弹性体具有理想的综合性能,可通过精心调整这些成分的比例来控制其性能。制备过程精简高效,使用的材料既经济又环保。这种弹性体具有良好的离子导电性(1.70 × 10-2-5.45 × 10-2 S m-1)、机械强度(0.48-1.21 兆帕断裂应力,395-701%断裂伸长率)、粘附能力(49-120 千帕粘附强度)以及对人体运动的感应灵敏度。
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来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
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