可穿戴技术
3D打印
可穿戴计算机
数码产品
材料科学
柔性电子器件
纳米技术
3d打印
计算机科学
嵌入式系统
工程类
复合材料
电气工程
生物医学工程
作者
Weiwei Cao,Lifang Lin,Herfried Lammer,Huihong Zhai,Dhandapani Kuzhandaivel,Xianmei Huang,Xuan Zhou,Zixiang Weng,Lixin Wu
标识
DOI:10.1021/acsapm.5c02172
摘要
Traditional ionogels often suffer from poor mechanical strength and low toughness, which limit their practical use in flexible devices. Although strategies such as constructing double-network and topological structures have improved the toughness of ionogels, their mechanical performance remains insufficient for wearable sensing applications under large stress and strain. To address this challenge, we propose a microphase separation-induced strategy to facilitate the formation of high-density hydrogen bonds. A bicontinuous-phase ionogel was synthesized via a one-step copolymerization method by combining acrylic acid (forming a solvent-rich phase) and a zwitterionic monomer (SPP) (forming a polymer-rich phase), which exhibited differential compatibility with ionic liquids. By leveraging synergistic hydrogen bonding and microphase separation, the ionogel achieves exceptional mechanical performance, with a tensile strength of 7.77 MPa, toughness of 40.24 MJ/m3, and fracture energy of 37.27 kJ/m2, surpassing most reported ionogels while maintaining crack insensitivity. Unlike the conventional ionogels used in sensing, the ionogel developed in this study maintained stable electrical signals even under 1000% strain. Moreover, the strong hydrogen bonding between the polar groups of the SPP segments endows the material with notch insensitivity (the notched samples still sustain 529% strain) and excellent adhesiveness, enabling direct skin contact for tape-free flexible sensors. This study provides a valuable design strategy for advancing ionogels in the field of wearable sensing.
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