材料科学
复合材料
韧性
脆性
复合数
聚合物
极限抗拉强度
弹性体
纳米复合材料
变形(气象学)
纳米颗粒
纳米纤维
芯(光纤)
粘弹性
压力(语言学)
模数
断裂韧性
粘附
天然橡胶
增韧
结构材料
纳米
聚乙烯醇
消散
聚合物纳米复合材料
聚酰亚胺
纳米反应器
纤维
纳米结构
软机器人
作者
S J Zhang,Xinyi Ji,Xiaoqian Mi,Weiqing Zhan,Peiqi Wu,Peng Lv,Huanhuan Gao,Xiangjian Wan,Wei Feng,Yiyu Feng,Jiajie Liang
摘要
ABSTRACT The intrinsic trade‐off between mechanical strengthening and toughening restricts the advancement of high‐performance polymer nanocomposites. Conventional rigid fillers often induce brittleness via stress concentrations, while liquid inclusions compromise load‐bearing capacity. To resolve this fundamental material paradox, we presented a bioinspired “rigid armor‐stretchable core” nanostructure architecture: liquid metal nanoparticles encapsulated by MXene nanosheets (LMNPs@MXene), synthesized via a thermodynamically driven, hyperbranched polymer‐mediated interfacial assembly. This hybrid design functioned as a dynamic interfacial stress regulator to alter the stress transfer paradigm within polymer matrices: the rigid MXene shell ensured robust interfacial adhesion and efficient load transfer, while the liquid core underwent adaptive, reversible deformation to serve as a high‐capacity energy dissipation sink. Upon integration into a polyvinyl alcohol matrix, the composite films exhibited a simultaneous breakthrough in tensile strength (58.1 MPa) and elongation at break (297.2%), culminating in a toughness of 102.8 MJ m −3 . This strategy proved universal across diverse matrices, ranging from brittle cellulose nanofibers to engineering polyimide and elastomeric polyurethane. Furthermore, the photothermal conversion capability of the hybrid filler endowed the composites with rapid, light‐triggered self‐healing properties. This work establishes a new paradigm for designing adaptive, stress‐managing materials, transcending the limits of static reinforcement.
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