Self-healable and freeze-resistant polyelectrolyte based on an EG anchor chain and dual dynamic reversible interaction as highly sensitive ionic skin

被引:8
作者
Liao, Haiyang [1 ,2 ]
Zhong, Wenzhao [1 ]
Han, Jieling [1 ]
Xiao, Yeqi [1 ]
Xiao, Tieming [1 ]
Sun, Xiao [1 ]
Cui, Guixin [2 ]
Huang, Jie [1 ]
机构
[1] Hunan Univ Technol, Sch Mech Engn, Zhuzhou 412007, Hunan, Peoples R China
[2] China Text Acad Zhejiang Technol Res Inst Co Ltd, Shaoxing 312071, Zhejiang, Peoples R China
关键词
FLEXIBLE SUPERCAPACITOR; HEALING HYDROGELS; STRAIN SENSORS; ORGANOHYDROGEL; ADHESIVE;
D O I
10.1039/d2tc05393d
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Presently, it is necessary to develop fully flexible sensors for the next generation of wearable electronics, and in this case, hydrogel-based flexible sensors are highly attractive due to their unique mechanical performances. However, the low-temperature freezing and bending fatigue of hydrogels severely hinder their application in flexible sensors. Herein, a polymeric dual-function hydrogel (DF-hydrogel) integrating self-healing and anti-freezing properties was prepared by building a dual dynamic network for application as ionic skin with excellent and reliable sensing performances. In DF-hydrogel, ethylene glycol (EG) and disulfide bonds were anchored in the molecular structure of double-bond-capped water-based polyurethane crosslinkers (DB-waPU) and subsequently introduced into the molecular backbone of the hydrogel via free radical polymerization. A multi-hydrogen bonding network was formed by the copolymerization of acrylamide with 2-ureido-4[1H]-pyrimidinone (UPy)-functionalized 1-vinylimidazole ionic liquid. Due to the dual dynamic network, DF-hydrogel exhibited exceptional self-healing capabilities and mechanical properties such as high healing efficiency, stretchability, compressibility, and self-adhesion. The anchored EG molecule in the polymer backbone endowed the hydrogel with intrinsic freeze-resistance without compromising its mechanical properties. The introduced poly(ionic liquid) provided free ions to the hydrogel, enhancing its ionic conductivity up to 9.6 mS cm(-1) in the absence of applied electrolyte salts. The DF-hydrogel-based ionic skins exhibited rapid, reversible, and dependable resistance changes with a wide range of strain sensing capabilities (10-300%). Moreover, a prototype 2D sensor array was fabricated to detect strains or pressures in two dimensions, strongly showing potential for the preparation of electronic skin, touch-pads, biosensors, and other applications.
引用
收藏
页码:4753 / 4765
页数:13
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