自愈水凝胶
材料科学
生物高聚物
共价键
化学工程
弹性体
纳米复合材料
壳聚糖
韧性
离子键合
复合材料
聚合物
高分子化学
化学
离子
有机化学
工程类
作者
Mehdihasan I. Shekh,Guangming Zhu,Wei Xiong,Weiling Wu,Florian J. Stadler,Dijit M. Patel,Chengtian Zhu
标识
DOI:10.1016/j.ijbiomac.2022.10.150
摘要
Biopolymer-based conductive hydrogels (HGs) are promising candidates for preparing environmentally friendly flexible electronics. However, it is still a great challenge to synthesize biopolymer-based tough, self-healable, and fast strain recoverable HGs. Herein, a facile strategy is demonstrated to synthesize stretchable, self-recoverable, conductive, and tough HGs strain sensors through the formation of multi-dynamic interactions (i.e., imine bond formation, hydrogen bonds, ionic bonds, and electrostatic bonds) and strong covalent interactions between MXene (Ti3C2Tx), oxidized sodium alginate (OSA), chitosan (CS), polyacrylamide (PAAm), Fe(III) and PEDOT:PSS. Thus, obtaining dynamically and covalently bonded nanocomposite hydrogels (NCHGs) with controllable interfacial interactions exhibited a high mechanical strength (0.91 MPa), toughness (2.99 MJ/m3), stretchability (820 %), elasticity (>600 %) and conductivity (1.31 S/m). In addition, the presence of Fe(III) ions and conducting fillers endows excellent repeatability with high stability in resistance change upon bending or stretching with ultra-broad sensitivity up to 11-gauge factor and consisting lowest resistance change up to 0.5 %.
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