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软质微颗粒自组装形成复杂的镶嵌结构。

Self-templating assembly of soft microparticles into complex tessellations.

机构信息

Laboratory for Soft Materials and Interfaces, Department of Materials, ETH Zurich, Zurich, Switzerland.

出版信息

Nature. 2020 Jun;582(7811):219-224. doi: 10.1038/s41586-020-2341-6. Epub 2020 Jun 11.

DOI:10.1038/s41586-020-2341-6
PMID:32528093
Abstract

Encoding Archimedean and non-regular tessellations in self-assembled colloidal crystals promises unprecedented structure-dependent properties for applications ranging from low-friction coatings to optoelectronic metamaterials. Yet, despite numerous computational studies predicting exotic structures even from simple interparticle interactions, the realization of complex non-hexagonal crystals remains experimentally challenging. Here we show that two hexagonally packed monolayers of identical spherical soft microparticles adsorbed at a liquid-liquid interface can assemble into a vast array of two-dimensional micropatterns, provided that they are immobilized onto a solid substrate one after the other. The first monolayer retains its lowest-energy hexagonal structure and acts as a template onto which the particles of the second monolayer are forced to rearrange. The frustration between the two lattices elicits symmetries that would not otherwise emerge if all the particles were assembled in a single step. Simply by varying the packing fraction of the two monolayers, we obtain not only low-coordinated structures such as rectangular and honeycomb lattices, but also rhomboidal, hexagonal and herringbone superlattices encoding non-regular tessellations. This is achieved without directional bonding, and the structures formed are equilibrium structures: molecular dynamics simulations show that these structures are thermodynamically stable and develop from short-range repulsive interactions, making them easy to predict, and thus suggesting avenues towards the rational design of complex micropatterns.

摘要

在自组装胶体晶体中对阿基米德和非正则镶嵌的编码有望为从低摩擦涂层到光电超材料的各种应用带来前所未有的结构依赖性特性。然而,尽管有许多计算研究预测了即使从简单的粒子间相互作用也能产生奇异结构,但复杂的非六边形晶体的实现仍然具有实验挑战性。在这里,我们表明,在液体-液体界面上吸附的相同球形软微粒子的两个六边形单层可以组装成大量二维微图案,只要它们一个接一个地固定在固体基底上。第一层保留其最低能量的六边形结构,并作为模板,迫使第二层的粒子在其上重新排列。两个晶格之间的干扰引发了如果所有粒子都在单个步骤中组装,则不会出现的对称性。只需改变两个单层的堆积分数,我们不仅可以获得低配位结构,如矩形和蜂窝晶格,还可以获得菱形、六边形和人字形超晶格,对非正则镶嵌进行编码。这是在没有定向键合的情况下实现的,并且形成的结构是平衡结构:分子动力学模拟表明,这些结构在热力学上是稳定的,并且由短程排斥相互作用发展而来,这使得它们易于预测,从而为复杂微图案的合理设计提供了途径。

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Using symmetry to elucidate the importance of stoichiometry in colloidal crystal assembly.利用对称性阐明化学计量比在胶体晶体组装中的重要性。
Nat Commun. 2019 May 2;10(1):2028. doi: 10.1038/s41467-019-10031-4.
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Microgels Adsorbed at Liquid-Liquid Interfaces: A Joint Numerical and Experimental Study.
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Capillary-driven self-assembly of soft ellipsoidal microgels at the air-water interface.毛细管驱动的软椭球形微凝胶在气-水界面的自组装。
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