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基于多重动态键的聚氨酯-氧化石墨烯网络具有超高机械强度和优异的室温自修复性能。

Ultrahigh Mechanical Strength and Robust Room-Temperature Self-Healing Properties of a Polyurethane-Graphene Oxide Network Resulting from Multiple Dynamic Bonds.

机构信息

Key Laboratory of Marine Materials and Related Technologies, Zhejiang Key Laboratory of Marine Materials and Protective Technologies, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, People's Republic of China.

University of Chinese Academy of Sciences, Beijing 100049, People's Republic of China.

出版信息

ACS Nano. 2022 Oct 25;16(10):16724-16735. doi: 10.1021/acsnano.2c06264. Epub 2022 Oct 10.

DOI:10.1021/acsnano.2c06264
PMID:36215403
Abstract

Addressing the conflict between achieving high mechanical properties and room-temperature self-healing ability is extremely significant to achieving a breakthrough in the application of self-healing materials. Therefore, inspired by natural spider silk and nacre, a room-temperature self-healing supramolecular material with ultrahigh strength and toughness is developed by synergistically incorporating flexible disulfide bonds and dynamic sextuple hydrogen bonds (H-bonds) into polyurethanes (PUs). Simultaneously, abundant H-bonds are introduced at the interface between graphene oxide nanosheets with dynamic multiple H-bonds and the PU matrix to afford strong interfacial interactions. The resulting urea-containing PU material with an inverse artificial nacre structure has a record mechanical strength (78.3 MPa) and toughness (505.7 MJ m), superior tensile properties (1273.2% elongation at break), and rapid room-temperature self-healing abilities (88.6% at 25 °C for 24 h), forming the strongest room-temperature self-healing elastomer reported to date and thus upending the previous understanding of traditional self-healing materials. In addition, this bionic PU-graphene oxide network endows the fabricated flexible intelligent robot with functional repair and shape memory capabilities, thus providing prospects for the fabrication of flexible functional devices.

摘要

解决在实现高机械性能和室温自修复能力方面的冲突,对于实现自修复材料的应用突破至关重要。因此,受天然蜘蛛丝和珍珠母启发,通过将柔性二硫键和动态六元氢键(H 键)协同纳入到聚氨酯(PU)中,开发出了一种具有超高强度和韧性的室温自修复超分子材料。同时,在具有动态多重 H 键的氧化石墨烯纳米片和 PU 基质的界面处引入了丰富的 H 键,以提供强大的界面相互作用。由此得到的含脲的具有反向人工珍珠母结构的 PU 材料具有创纪录的机械强度(78.3 MPa)和韧性(505.7 MJ m)、优异的拉伸性能(断裂伸长率 1273.2%)和快速的室温自修复能力(在 25°C 下 24 小时自修复率 88.6%),形成了迄今为止报道的最强室温自修复弹性体,从而颠覆了传统自修复材料的已有认知。此外,这种仿生 PU-氧化石墨烯网络赋予了所制备的柔性智能机器人功能性修复和形状记忆能力,从而为柔性功能器件的制造提供了前景。

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