Self-assembly of anisotropic tethered nanoparticle shape amphiphiles

被引:160
作者
Glotzer, SC [1 ]
Horsch, MA
Iacovella, CR
Zhang, ZL
Chan, ER
Zhang, X
机构
[1] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/j.cocis.2005.09.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The varied and exotic shapes of new nanoscale organic and inorganic building blocks provide new opportunities to engineer materials possessing specific functionality and physical properties dictated by the unique packings of these particles. We briefly review some of the current strategies for inducing the self-assembly of these building blocks focusing on one strategy in particular-the attachment of tethers to the building blocks at precise locations to create tethered nanoparticle "shape amphiphiles". We use Computer simulation to demonstrate that the resulting anisotropy imparted to nanocrystals or nanocolloids by the tethers can be used to encode simple design rules into the building blocks that ultimately result in a unique self-assembled structure. We present a general classification scheme for tethered nanoparticles wherein the anisotropy of a shape amphiphile is described by a vector comprised of one or more axes each describing a measure of anisotropy. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:287 / 295
页数:9
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