化学工程
壳聚糖
化学
共晶体系
铵
材料科学
可穿戴计算机
生物相容性材料
高分子化学
傅里叶变换红外光谱
作者
Peng Liu,Decai Zou,Changxiu Chen,Wenlong Zhang,Xiangqun Ding,Ning Tang,Hui Li,Lili Gao,Yunwu Yu
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2026-06-25
卷期号:27 (7): 4650-4661
被引量:1
标识
DOI:10.1021/acs.biomac.6c00606
摘要
Hydrogel adhesives that simultaneously possess high toughness, strong interfacial adhesion, and freeze resistance are urgently needed for emerging flexible electronics and wearable devices. However, conventional hydrogels typically suffer from weak bonding to diverse substrates and brittle failure under subzero conditions. Herein, we present a cation–dipole-enhanced eutectic organohydrogel (APQ-DES) constructed via an interpenetrating network strategy using a choline chloride/glycerol deep eutectic solvent (DES) as the dispersion medium. The system combines chemically cross-linked polyacrylamide (PAM), poly(vinyl alcohol) (PVA), and cationic quaternary ammonium chitosan (QCS). The DES endows the hydrogel with excellent freeze tolerance, while synergistic cation–dipole interactions between QCS and various substrates, together with hydrogen bonding from PVA and PAM, enable robust adhesion across diverse materials, including PTFE, rubber, glass, and wood, achieving lap-shear strengths up to 584.57 kPa. The optimized APQ-DES hydrogel exhibits outstanding mechanical properties (tensile strength: 206.99 kPa, elongation at break: 1891%, toughness: 1.71 MJ·m –3 ), maintains flexibility and ionic conductivity at −20 °C, and functions as a reliable strain sensor with rapid response (361 ms), broad sensing range (0–400% strain), and stable cyclic performance. Demonstrations of multisite human motion monitoring under cold conditions highlight its potential for winter sports training evaluation, human–machine interfaces, and low-temperature wearable healthcare applications.
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