聚合物
材料科学
粒子(生态学)
纳米颗粒
聚合物纳米复合材料
纳米复合材料
复合材料
化学工程
韧性
吸附
粒径
纳米技术
色散(光学)
作者
Quanyin Xu,Hongbo Qu,Zhenghao Wu,Zhen Zhao,Sisi Ge,Jintian Luo,Biao Zuo
标识
DOI:10.1038/s41467-025-64841-w
摘要
Polymer nanocomposites (PNCs) benefit from the enhanced properties originating from the synergistic effects of nanoparticles (NPs) and a polymer matrix. However, the incorporation of NPs slows PNC relaxation, and particularly at high-particle-loading, the PNC melts become non-flowing because the interfacially adsorbed polymers bridge the particles, generating a kinetically quasi-permanent particle network. Herein, by introduction of bound polymer loops on the NP surfaces, we molecularly design a relaxation-enhanced PNC, where interfacial polymers adhering to the NP surfaces freely relaxed, enabling formation of a dynamic, loose particle network that facilitates flow of the PNC melts. The resultant molten high-NP-loading composites maintain fluid-like and low-viscosity dynamics, while the corresponding glassy materials possess enhanced toughness and strength. Thus, the demonstrated principle of preparing relaxation-enhanced PNCs by optimizing the way by which polymers are attached to the filler surface represents the state-of-the-art strategy for overcoming the tradeoff between the processability and mechanical performance of PNCs.
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