粘弹性
材料科学
纳米技术
聚合物
纳米颗粒
放松(心理学)
连接器
拓扑(电路)
网络拓扑
分子动力学
星团(航天器)
分子工程
应力松弛
计算机科学
化学
复合材料
计算化学
工程类
心理学
社会心理学
蠕动
电气工程
程序设计语言
操作系统
作者
Jia‐Fu Yin,Wei Liu‐Fu,Junsheng Yang,Yuyan Lai,Binghui Xue,Haiyan Xiao,Qing‐Yun Guo,Yuchu Liu,Panchao Yin
标识
DOI:10.1021/acs.jpclett.4c00833
摘要
The search for alternative chemical systems other than polymers with chain topologies for soft structural materials raises general interests in fundamental materials and chemical sciences. It is also appealing from an engineering perspective for the urgent need to resolve the typical trade-offs of polymer systems. Herein, a subnanometer molecular cluster, polyhedral oligomeric silsesquioxanes, is assembled into molecular nanoparticles (MNPs) with star topology. Broadly tunable viscoelasticity can be realized by fine-tuning the MNPs' deformability. Being analogous to polymeric systems, the hierarchical structural relaxation dynamics can be observed, and their relaxation time and temperature dependence are dominated by the linker flexibilities. This not only provides microscopic understanding on MNP's unique viscoelasticity but also offers enormous opportunities for modulating their mechanical properties via linker engineering. Our work proves the possibility of applying structural units with particle topologies for the design of soft structural materials.
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