聚氨酯
弹性体
材料科学
复合数
聚合物
导电体
极限抗拉强度
碳纳米管
复合材料
电阻率和电导率
变形(气象学)
电导率
兴奋剂
纳米复合材料
导电聚合物
先进复合材料
机械强度
纳米技术
人工肌肉
碳纤维
超分子化学
共价键
作者
Mingfa Hou,Peiwen Li,Yujie Zhang,Chen Zhang,Zhi‐Hui Ren,Zheng‐Hui Guan
标识
DOI:10.1021/acsapm.5c02970
摘要
Polymeric materials integrating high mechanical strength, electrical conductivity, and self-healing capabilities demonstrate significant potential for advanced flexible electronics. Nevertheless, concurrent optimization of these mutually exclusive properties remains a critical challenge in materials design. A UV-responsive self-healing polyurethane elastomer (HEOMC-0.5) was synthesized via one-pot copolymerization, incorporating multiple hydrogen bonds and coumarin-derived photoreversible cross-links. Subsequent integration of carbon nanotubes (CNTs, 5 wt %) yielded an electrically conductive composite (HEOMC-0.5-CNTs). The composite exhibited exceptional mechanical (a mechanical strength of 28.42 MPa and a tensile strain of 1528.57%) and self-healing properties (a healing efficiency of 88.99%). Upon doping with CNTs, it possessed an electrical conductivity of 0.2098 mS/cm. Due to the self-healing property of HEOMC-0.5-CNTs, it can act as a “switch” in the circuit to control the lighting on and off of small bulbs through its healing ability. This synergistic design combines dynamic covalent networks with supramolecular interactions, enabling multifunctional polyurethanes. The integrated mechanical, electrical, and self-healing performance establishes a versatile strategy for advanced flexible electronics.
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