Micro- and nanoparticles self-assembly for virtually defect-free, adjustable monolayers

被引:86
作者
Aubry, N. [1 ]
Singh, P. [2 ]
Janjua, M. [2 ]
Nudurupati, S. [2 ]
机构
[1] Carnegie Mellon Univ, Dept Mech Engn, Pittsburgh, PA 15213 USA
[2] New Jersey Inst Technol, Dept Mech Engn, Newark, NJ 07102 USA
关键词
capillarity; electrohydrodynamics; nanotechnology; nanocrystal; dipole-dipole interactions;
D O I
10.1073/pnas.0712392105
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
As chips further shrink toward smaller scales, fabrication processes based on the self-assembly of individual particles into patterns or structures are often sought. One of the most popular techniques for two-dimensional assembly (self-assembled monolayers) is based on capillary forces acting on particles placed at a liquid interface. Capillarity-induced clustering, however, has several limitations: it applies to relatively large (radius > approximate to 10 mu m) particles only, the clustering is usually non-defect-free and lacks long-range order, and the lattice spacing cannot be adjusted. The goal of the present article is to show that these shortcomings can be addressed by using an external electric field normal to the interface. The resulting self-assembly is capable of controlling the lattice spacing statically or dynamically, forming virtually defect-free monolayers, and manipulating a broad range of particle sizes and types including nanoparticles and electrically neutral particles.
引用
收藏
页码:3711 / 3714
页数:4
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