发光
材料科学
聚氨酯
韧性
离子键合
氢键
聚合物
纳米技术
化学工程
复合材料
分子
光电子学
化学
有机化学
离子
工程类
作者
Ting Ye,Jiayin Liu,Juan‐Juan Sun,Jialing Tan,Xin Chen,Yunjie Yin,Chaoxia Wang
标识
DOI:10.1016/j.cej.2023.146393
摘要
Luminescent materials display their fascinating performance in wearable electronics, optoelectronics, and information interactions. Enhancing reliability and longevity is particularly attractive for next-generation luminescent polymeric materials. Here we fabricate a supramolecular healable, luminescent waterborne polyurethane (Supra-LWPU) by incorporating reversible hydrogen bonds and ionic interactions into the noncovalent crosslinking network. The Supra-LWPU polymer exhibits excellent mechanical performance with robust tensile strength (6.8 MPa), superior stretchability (1755.4 %), high toughness (70.9 MJ m−3), and damage tolerance (44.7 KJ m−2). Owing to the sacrificial and reversible hard domains, the damaged network demonstrates a dynamic rearrangement with efficient healing efficiency (92.1 %), accompanying the restored toughness (65.3 MJ m−3) at 60 °C after 24 h. Multiple H-bonds induce aggregation domain formation of tertiary amine groups, rendering a luminous polyurethane network. An aggregate luminescence behavior can effectively assist in observing the healing process of Supra-LWPU networks. The mechanically responsive luminescent (MRL) device with well-organized microcracks exhibits strain-dependent luminescence for fluorescent patterns, demonstrating promise in next-generation stimuli responsive light-emitting materials.
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