韧性
消散
自愈水凝胶
磁滞
量子纠缠
极限抗拉强度
纳米技术
材料科学
物理
复合材料
量子
凝聚态物理
热力学
高分子化学
量子力学
作者
Zhu Ruixin,Dandan Zhu,Zhen Zheng,Xinling Wang
标识
DOI:10.1038/s41467-024-45485-8
摘要
Abstract Most tough hydrogels are reinforced by introducing energy dissipation mechanisms, but simultaneously realizing a high toughness and low hysteresis is challenging because the energy dissipation structure cannot recover rapidly. In this work, high mechanical performance highly entangled double network hydrogels without energy dissipation structure are fabricated, in which physical entanglements act as the primary effective crosslinking in the first network. This sliding entanglement structure allows the hydrogel network to form a highly uniform oriented structure during stretching, resulting in a high tensile strength of ~3 MPa, a fracture energy of 8340 J m −2 and a strain-stiffening capability of 47.5 in 90% water content. Moreover, almost 100% reversibility is obtained in this hydrogel via energy storage based on entropy loss. The highly entangled double network structure not only overcomes the typical trade-off between the high toughness and low hysteresis of hydrogels, but more importantly, it provides an insight into the application of entanglement structures in high-performance hydrogels.
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