Healable, luminescent, notch-insensitive waterborne polyurethane via noncovalent crosslinking with hydrogen bonds and ionic interactions

被引:27
|
作者
Ye, Ting [1 ]
Liu, Jiayin [1 ]
Sun, Juanjuan [1 ]
Tan, Jialing [1 ]
Chen, Xin [1 ]
Yin, Yunjie [1 ]
Wang, Chaoxia [1 ]
机构
[1] Jiangnan Univ, Coll Text Sci & Engn, 1800 Lihu Rd, Wuxi 214122, Peoples R China
基金
美国国家科学基金会;
关键词
Waterborne polyurethane; Self-healing; Damage tolerance; Crack diagnosis; Light-emitting materials; SELF-HEALING ELASTOMERS; TOUGH; EVOLUTION; ACID;
D O I
10.1016/j.cej.2023.146393
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
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 degrees 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.
引用
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页数:11
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