材料科学
复合材料
弹性体
电阻式触摸屏
炭黑
导电体
延伸率
胶粘剂
聚氨酯
断裂(地质)
机械强度
工作(物理)
标度系数
二硫键
阳极
比强度
极限抗拉强度
碳纤维
断裂强度
作者
Yufei Cao,Pengyu Zhu,Shuo Yang,Wenwen Wu,Dongli Fan,Peng Zhu,Haiyan Ma,H J Lu,Jie Liu,Yufeng Cao,Tao Qian
标识
DOI:10.1021/acsapm.6c01612
摘要
Conventional flexible sensors often face a compromise between mechanical properties and self-healing ability, which severely limits their long-term usability and functional reliability. In this work, we report a series of polyurethane elastomers synergistically reinforced by multiple hydrogen bonds and disulfide bonds, which integrates high mechanical strength and autonomous self-healing ability. The optimized composition, PU-BHO 0.3 -BHDS 0.7, achieved an excellent breaking strength of ∼39.73 MPa, an elongation at break of ∼1568.61%, and a fracture energy of ∼157.75 kJ·m –2 . It also exhibited an ultrahigh self-healing efficiency of ∼99.29% at room-temperature, retaining ∼85.90% even at −18 °C. Based on this elastomer, we fabricated a multilayer resistive sensor using liquid gallium (LG) and carbon black (CB) as conductive electrodes. The healed sensor maintained a gauge factor and resistance response nearly identical to its original state, demonstrating complete functional restoration. This work provides a feasible strategy for developing high-performance self-healing materials suitable for durable flexible electronic devices, such as human motion sensors.
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