材料科学
自愈水凝胶
韧性
磁滞
复合材料
极限抗拉强度
电容感应
磷酸
聚合物
聚合
单体
压力传感器
人工肌肉
压力(语言学)
变形(气象学)
作者
Chengdong Ma,Hongrui Zhang,Weigui Xie,Wangyu Liu
标识
DOI:10.1021/acsapm.6c00806
摘要
Phosphoric acid-based ion-conductive hydrogels face a long-standing challenge of balancing toughness, low hysteresis, and high conductivity, which are key requirements for advanced flexible sensing materials. In this work, a tough and low-hysteresis acrylamide-phosphoric acid (AP) hydrogel is proposed, using an ultralow-initiator-concentration (0.005 wt % relative to the monomer mass) polymerization method. Swelling, SAXS, and SEM experiments confirm the uniform chains, and FT-IR experiments demonstrate a strong hydrogen-bonding network of our ultralow-initiator-concentration-polymerized AP hydrogel. Uniaxial tensile tests show that the toughness and hysteresis of the AP hydrogel are inversely associated with the initiator concentration. Consequently, the ultralow-initiator-concentration-enabled AP hydrogel presents a tensile strength of 2.1 MPa, a toughness of 8.9 MJ m –3, and an ultralow hysteresis of 1.35% under 100% strain. Benefiting from the excellent electromechanical properties, the AP hydrogel-based flexible sensor exhibits high reliability as a flexible resistance strain sensor and an electric double-layer capacitive pressure sensor. This work not only resolves the inherent constraint of traditional phosphoric acid-based hydrogels but also provides a perspective for the structural regulation of functional hydrogels, enabling broader applications in flexible sensing and human–machine interactions.
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