平面的
极化(电化学)
分子
胶体
材料科学
纳米技术
光电子学
化学工程
化学
计算机科学
工程类
有机化学
物理化学
计算机图形学(图像)
作者
Xi Chen,Xianghong Liu,Mohd Yasir Khan,Zuyao Yan,Dezhou Cao,Shifang Duan,Lingshan Fu,Wei Wang
出处
期刊:Research
[American Association for the Advancement of Science]
日期:2024-01-01
卷期号:7
被引量:1
标识
DOI:10.34133/research.0490
摘要
Colloidal molecules, ordered structures assembled from micro- and nanoparticles, serve as a valuable model for understanding the behavior of real molecules and for constructing materials with tunable properties. In this work, we introduce a universal strategy for assembling colloidal molecules consisting of a central active particle surrounded by several passive particles as ligands. During the assembly process, active particles attract the surrounding passive particles through phoresis and osmosis resulting from the chemical reactions on the surface of the active particles, while passive particles repel each other due to the electric polarization induced by an alternating current (AC) electric field. By carefully selecting particles of varying structures and sizes, we have assembled colloidal molecules of symmetric and asymmetric dimers, trimers, and multimers. Furthermore, the coordination number of these colloidal molecules can be regulated in real time and in situ by tuning the interaction forces between the constituent particles. Brownian dynamics simulations reproduced the formation of the colloidal molecules and validated that the self-assembly arises from chemically induced attraction and electrical dipolar repulsion. This strategy for reconfigurable colloidal assemblies poses the potential for designing adaptive micro-nanomachines.
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