Shape-Controlled Colloidal Interactions in Nematic Liquid Crystals

被引:275
|
作者
Lapointe, Clayton P. [1 ,2 ,3 ,4 ]
Mason, Thomas G. [3 ,4 ]
Smalyukh, Ivan I. [1 ,2 ]
机构
[1] Univ Colorado, Dept Phys, Renewable & Sustainable Energy Inst, Boulder, CO 80309 USA
[2] Univ Colorado, Liquid Crystals Mat Res Ctr, Boulder, CO 80309 USA
[3] Univ Calif Los Angeles, Dept Chem & Biochem, Dept Phys & Astron, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Calif NanoSyst Inst, Los Angeles, CA 90095 USA
基金
美国国家科学基金会;
关键词
D O I
10.1126/science.1176587
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Robust control over the positions, orientations, and assembly of nonspherical colloids may aid in the creation of new types of structured composite materials that are important from both technological and fundamental standpoints. With the use of lithographically fabricated equilateral polygonal platelets, we demonstrate that colloidal interactions and self-assembly in anisotropic nematic fluids can be effectively tailored via control over the particles' shapes. The particles disturb the uniform alignment of the surrounding nematic host, resulting in both a distinct equilibrium alignment and highly directional pair interactions. Interparticle forces between polygonal platelets exhibit either dipolar or quadrupolar symmetries, depending on whether their number of sides is odd or even, and drive the assembly of a number of ensuing self-assembled colloidal structures.
引用
收藏
页码:1083 / 1086
页数:4
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