Xing Yuedong, Li Jiongchao, Cheng Jie, Lu Liwei, Xue Tao, Xu Jianben, Xu Xiang, Zhang Faai
Key Laboratory of New Processing Technology for Nonferrous Metal and Materials, Ministry of Education, Guangxi Key Laboratory of Optical and Electronic Materials and Devices, Guangxi Colleges and Universities Key Laboratory of Natural and Biomedical Polymer Materials, College of Material Science and Engineering, Guilin University of Technology, Guilin, Guangxi, 541004, China.
College of Chemistry and Biology Engineering, Guilin University of Technology, Guilin, Guangxi, 541004, China.
Small. 2025 Feb;21(5):e2411040. doi: 10.1002/smll.202411040. Epub 2024 Dec 12.
High-performance elastomers with exceptional mechanical properties and self-healing capabilities have garnered significant attention due to their wide range of potential applications. However, designing elastomers that strike a balance between self-healing capabilities and mechanical properties remains a considerable challenge. Inspired by biological cartilage, a highly robust, tough, and crack-resistant self-healing elastomer is presented by incorporating hydrogen-bond-rich 2D polyamide (2DPA) into a poly(urethane-urea) matrix. This integration enhances supramolecular interactions driven by multiple hydrogen bonds. The resulting elastomer exhibits impressive strength (54.6 MPa), remarkable elongation at break (705.4%), exceptional toughness (116.7 MJ m), outstanding crack resistance (fracture energy up to 187.2 kJ m), high self-healing efficiency (98.9% at 50 °C for 9 h, 97.9% at room temperature for 48 h), and excellent recyclability, capable of lifting ≈40 000 times its own weight. Furthermore, a damage-tolerant, fatigue-resistant anticorrosive coating from this elastomer, showcasing its potential for protective skin applications in underwater robotics is developed. The underlying enhancement mechanism is validated through testing of various elastomers and molecular dynamics simulations, confirming the potential of engineering 2DPA for high-performance elastomers by leveraging supramolecular interactions.
具有卓越机械性能和自修复能力的高性能弹性体因其广泛的潜在应用而备受关注。然而,设计出在自修复能力和机械性能之间取得平衡的弹性体仍然是一项重大挑战。受生物软骨的启发,通过将富含氢键的二维聚酰胺(2DPA)融入聚(脲氨酯)基体中,制备出了一种高度坚固、坚韧且抗裂的自修复弹性体。这种结合增强了由多个氢键驱动的超分子相互作用。所得弹性体表现出令人印象深刻的强度(54.6兆帕)、显著的断裂伸长率(705.4%)、出色的韧性(116.7兆焦/平方米)、卓越的抗裂性(断裂能高达187.2千焦/平方米)、高自修复效率(50℃下9小时为98.9%,室温下48小时为97.9%)以及出色的可回收性,能够承受约其自身重量40000倍的重量。此外,还开发了一种由这种弹性体制成的耐损伤、抗疲劳的防腐涂层,展示了其在水下机器人防护皮肤应用中的潜力。通过对各种弹性体的测试和分子动力学模拟验证了潜在的增强机制,证实了利用超分子相互作用设计用于高性能弹性体的二维聚酰胺的潜力。