木质素
竹子
材料科学
超分子化学
数码产品
聚合物
纳米技术
高分子科学
复合材料
化学
有机化学
分子
物理化学
作者
Zhimin Kou,Ye Sha,Lihong Hu,Meiting Liu,Fuchun Huang,Jie Wang,Caiying Bo,Yonghong Zhou,Dawei Zhao,Puyou Jia
出处
期刊:PubMed
日期:2025-09-12
卷期号:: e12983-e12983
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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