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Engineering PDA@CNTs-Enhanced sulfobetaine methacrylate hydrogels for superior flexible sensor applications

自愈水凝胶 甲基丙烯酸酯 生物相容性 材料科学 复合数 高分子化学 胶粘剂 碳纳米管 纳米技术 化学工程 单体 复合材料 聚合物 图层(电子) 工程类 冶金
作者
Jian Liu,Xiao Wang,Kai Han,Jing Liu,Jinfeng Yuan,Mingwang Pan,Zhicheng Pan
出处
期刊:Polymer [Elsevier]
卷期号:311: 127482-127482 被引量:8
标识
DOI:10.1016/j.polymer.2024.127482
摘要

Conductive hydrogels have attracted significant attention as versatile materials for flexible sensors, with potential implementation in wearable technologies, electronic skins, and health diagnostics. However, traditional hydrogel models are frequently limited by their inadequate mechanical strength, poor conductivity, weak adhesion, and low durability, which pose significant barriers to their further application in flexible sensors. In this work, we prepared composite multifunctional hydrogels as flexible sensors, which were synthesized from sulfobetaine methacrylate SBMA) and acrylamide (AM), infused with dodecyl quaternary ammonium salt (Q12), and incorporated with poly(dopamine)-functionalized carbon nanotubes (PDA@CNTs). The PDA modification enhances the compatibility of CNTs with the hydrogel matrix. The incorporation of PDA@CNTs into the hydrogel matrix, along with the establishment of multiple dynamic bonds—such as ionic bonds, hydrogen bonds, cation-π interactions, and π-π stacking between polymer chains and PDA moieties—significantly enhances its tensile strength (53.79 kPa), toughness (134.77 kJ/m3), adhesive capabilities (29.84 kPa to paper), and electrical conductivity (0.2 S/m). Moreover, the composite hydrogel reveals a remarkable mechanical strain response, coupled with impressive stability and durability over prolonged periods. It efficiently differentiates between mild elongations (10%–40 %) and substantial elongations (50%–300 %), thereby showcasing its capability for real-time biomechanical motion monitoring. Additionally, the composite hydrogel displays remarkable photothermal antibacterial efficacy upon exposure to near-infrared (NIR) radiation, along with outstanding biocompatibility under standard conditions, thereby confirming its suitability for safe and long-term biological interactions. The exceptional functionality of these composite hydrogels renders them highly conducive to diverse applications in the realm of wearable sensor technologies.
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