Fabrication of dual dynamic crosslinking polyurethane networks towards self-healing, resist fatigue, and highly stretchable ionic skins

IF 4.1 2区 化学 Q2 POLYMER SCIENCE Polymer Pub Date : 2024-08-15 DOI:10.1016/j.polymer.2024.127506
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Abstract

The limited anti-fatigue performance of self-healing polyurethane elastomers under high-strain conditions restricts their application in high-performance ionic skins. Herein, a polyurethane network (PU-DDN) synergistically reversibly crosslinked by dynamic thiourethane bonds and hydrogen bonds was synthesized successfully. This dual reversibly crosslinking strategy not only endowed the polyurethane network with an excellent fatigue resistance (showing a residual strain of only 63 % after 10 uninterrupted cyclic tensile tests at 400 % strains), but also imparted it with a high strength (6.12 MPa) and stretchability (611.42 %). Owing to the thermo-reversibility of dual dynamic networks, the damaged PU-DDN heated at 100 °C for 3h could fully restore its initial mechanical properties. Subsequently, transparent stretchable ionic skins were fabricated by mixing the PU-DDN with ionic liquids. A resulting highly-sensitive ionic skin (GF1 = 1.25, GF2 = 2.01) named PU-DDN/IL20 demonstrated exceptional durability, which could produce repeatable electrical signals even after 2000 cycles of stretching to an extensive deformation of 400 %. Meanwhile, it can also monitor human motions, showcasing its promising potential in the realm of intelligent wearable applications.

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制造双动态交联聚氨酯网络,实现自愈合、抗疲劳和高拉伸性离子表皮
自愈合聚氨酯弹性体在高应变条件下的抗疲劳性能有限,限制了其在高性能离子表皮中的应用。本文成功合成了一种通过动态硫代氨基甲酸酯键和氢键协同可逆交联的聚氨酯网络(PU-DDN)。这种双重可逆交联策略不仅赋予了聚氨酯网络极佳的抗疲劳性(在 400 % 的应变下进行 10 次不间断循环拉伸试验后,残余应变仅为 63 %),还赋予了其高强度(6.12 兆帕)和拉伸性(611.42 %)。由于双动态网络的热可逆性,在 100 °C 下加热 3 小时后,受损的聚氨酯-DDN 可完全恢复其初始机械性能。随后,通过将 PU-DDN 与离子液体混合,制备出了透明的可拉伸离子表皮。制备出的高灵敏度离子表皮(GF1 = 1.25,GF2 = 2.01)被命名为 PU-DDN/IL20,具有超强的耐久性,即使经过 2000 次拉伸至 400% 的大变形,也能产生可重复的电信号。同时,它还能监测人体运动,在智能可穿戴应用领域大有可为。
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来源期刊
Polymer
Polymer 化学-高分子科学
CiteScore
7.90
自引率
8.70%
发文量
959
审稿时长
32 days
期刊介绍: Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics. The main scope is covered but not limited to the following core areas: Polymer Materials Nanocomposites and hybrid nanomaterials Polymer blends, films, fibres, networks and porous materials Physical Characterization Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films Polymer Engineering Advanced multiscale processing methods Polymer Synthesis, Modification and Self-assembly Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization Technological Applications Polymers for energy generation and storage Polymer membranes for separation technology Polymers for opto- and microelectronics.
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