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形状诱导变形、毛细桥接以及在流体-流体界面处的长方体自组装。

Shape-Induced Deformation, Capillary Bridging, and Self-Assembly of Cuboids at the Fluid-Fluid Interface.

机构信息

Polymer Engineering and Colloid Science (PECS) Laboratory, Department of Chemical Engineering, Indian Institute of Technology Madras , Chennai 600 036, India.

出版信息

Langmuir. 2017 Jan 24;33(3):791-801. doi: 10.1021/acs.langmuir.6b03866. Epub 2017 Jan 12.

Abstract

The controlled assembly of anisotropic particles through shape-induced interface deformations is shown to be a potential route for the fabrication of novel functional materials. In this article, the shape-induced interface deformation, capillary bridging, and directed self-assembly of cuboidal-shaped hematite particles at fluid-fluid interfaces are reported. The multipolar nature of the interface distortions is directly visualized using high-resolution scanning electron microscopy and 3D optical surface profiling. The nature of the interface deformations around cuboidal particles vary from monopolar to octupolar types depending on their orientation and position with respect to the interface. The deformations are of either hexapolar or octupolar type in the face-up orientation, quadrupolar or monopolar type in the edge-up orientation, and monopolar type in the vertex-up orientation. The particles adsorbed at the interface interact through the interface deformations, forming capillary bridges that lead to isolated assemblies of two or more particles. The arrangement of particles in any assembly is such that the condition for capillary attraction is satisfied, that is, in accordance with predictions based on the nature of interface deformations. At sufficient particle concentrations, these isolated structures interact to form a percolating network of cuboids. Furthermore, the difference in the nature of the assembly structures formed at the air-water interface and in the bulk water phase indicates that the interfacial assembly of these particles is controlled by the capillary interactions.

摘要

通过形状诱导的界面变形来控制各向异性颗粒的组装被证明是制造新型功能材料的一种有前途的方法。本文报道了在液-液界面上通过各向异性的四角形赤铁矿颗粒的形状诱导界面变形、毛细桥作用和定向自组装。使用高分辨率扫描电子显微镜和 3D 光学表面轮廓仪直接可视化了界面变形的多极性质。界面变形的性质可以是单极的或八极的,这取决于颗粒的取向和相对于界面的位置。在面朝上的取向中,变形是六极或八极的,在边朝上的取向中是四极或单极的,在顶点朝上的取向中是单极的。吸附在界面上的颗粒通过界面变形相互作用,形成毛细桥,导致两个或更多颗粒的孤立组装。在任何组装体中,颗粒的排列方式都满足毛细吸引力的条件,即符合基于界面变形性质的预测。在足够高的颗粒浓度下,这些孤立的结构相互作用形成一个具有渗透性的四角形长方体网络。此外,在空气-水界面和本体水相中形成的组装结构的性质的差异表明,这些颗粒的界面组装受到毛细相互作用的控制。

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