Controlled growth of hard-sphere colloidal crystals

被引:188
作者
Cheng, ZD
Russell, WB
Chaikin, PM [1 ]
机构
[1] Princeton Univ, Dept Phys, Princeton, NJ 08540 USA
[2] Princeton Univ, Dept Chem Engn, Princeton, NJ 08540 USA
关键词
D O I
10.1038/44785
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
Three-dimensional ordered colloidal systems with lattice, constants comparable to the wavelength of visible light might find important application as photonic crystals(1), optic filters and switches(2), and chemical sensors(3). Colloidal crystallization has been actively studied(4-8), leading to the development of several methods to control the self-assembly of the colloidal particles; examples include colloidal epitaxy(9) and space-based reduced-gravity techniques(10,11). Here we report a method to control the nucleation and growth of hard-sphere colloidal crystals that relies on the use of temperature gradients to define a density gradient. This is somewhat counterintuitive as temperature does not play a role in determining the hard-sphere phase diagram. We obtain hard-sphere single crystals (size similar to 3mm) from a sample in a concentration regime that would remain in the liquid state in the absence of a temperature gradient. We expect the method to have applications in controlling the ordering and growth of various 'soft' systems including colloids, copolymers, emulsions and proteins.
引用
收藏
页码:893 / 895
页数:3
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