木质素
柔性电子器件
材料科学
超分子化学
数码产品
聚合物
氢键
软机器人
超分子聚合物
纳米技术
生物电子学
灵活的显示器
离子键合
倍半硅氧烷
可扩展性
硫系化合物
人工肌肉
电子皮肤
软质材料
粘附
纳米颗粒
纳米结构
化学工程
可穿戴技术
胶粘剂
层状结构
无定形固体
纳米复合材料
复合材料
作者
Zhimin Kou,Ye Sha,Lihong Hu,Meiting Liu,Fuchun Huang,Jie Wang,Caiying Bo,Yonghong Zhou,Dawei Zhao,Puyou Jia
标识
DOI:10.1002/advs.202512983
摘要
Ionogels have emerged as a groundbreaking category of materials for flexible electronics, yet the challenge of integrating high mechanical stretchability, rapid electrical response, and reliable self-repair in bio-based ionogels persists. Here, a lignin-derived ionogel is presented, designated P(LA-TA)-gel, through a straightforward, one-step solvent-free process. By leveraging arginine-grafted lignin-terminated polythioctic acid and incorporating imine and hydroxyl groups into the supramolecular framework, the P(LA-TA)-gel with both dynamic disulfide bonds and supramolecular hydrogen bonds achieves effective energy dissipation channels. This configuration adeptly balances mechanical stretchability-exhibiting a strain of 1233%-with dynamic reversibility, evidenced by an adhesion strength of 335.5 kPa. Notably, the P(LA-TA)-gel showcases rapid response characteristics, achieving a response time of 0.1 s, along with high ionic conductivity of 17.36 mS cm-1 and robust self-healing capabilities exceeding 90%. When utilized in flexible sensors, this ionogel demonstrates a wide response range and high sensitivity. This study establishes a sustainable platform for the development of next-generation flexible sensors and highlights significant potential applications across wearable electronics, electronic skin technology, and soft robotics.
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