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Liquid crystal order in colloidal suspensions of spheroidal particles by direct current electric field assembly

机译:直流电场在球体胶体悬浮液中的液晶顺序

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DC electric fields are used to produce colloidal assemblies with orientational and layered positional order from a dilute suspension of spheroidal particles. These 3D assemblies, which can be visualized in situ by confocal microscopy, are achieved in short time spans (t < 1 h) by the application of a constant voltage across the capacitor-like device. This method yields denser and more ordered assemblies than had been previously reported with other assembly methods. Structures with a high degree of orientational order as well as layered positional order normal to the electrode surface are observed. These colloidal structures are explained as a consequence of electrophoretic deposition and field-assisted assembly. The interplay between the deposition rate and the rotational Brownian motion is found to be critical for the optimal ordering, which occurs when these rates, as quantified by the Peclet number, are of order one. The results suggest that the mechanism leading to ordering is equilibrium self-assembly but with kinetics dramatically accelerated by the application of the DC electric field. Finally, the crystalline symmetry of the densest structure formed is determined and compared with previously studied spheroidal assemblies.
机译:DC电场用于从球形颗粒的稀悬液中产生具有定向和分层位置顺序的胶体组件。这些3D组件可以通过共聚焦显微镜在现场看到,通过在类似电容器的设备上施加恒定电压,可以在较短的时间跨度(t <1 h)内实现。与以前使用其他组装方法所报告的方法相比,此方法可产生更密集和更有序的组装。观察到具有垂直于电极表面的高度取向次序以及分层位置次序的结构。这些胶体结构是电泳沉积和现场辅助组装的结果。发现沉积速率和旋转布朗运动之间的相互作用对于最佳排序是至关重要的,最佳排序发生在当这些速率(由佩克雷特数量化)为一阶时。结果表明,导致有序化的机制是平衡自组装,但是通过施加直流电场,其动力学急剧加快。最后,确定所形成的最致密结构的晶体对称性,并将其与先前研究的球状组件进行比较。

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