Mechanism for hierarchical self-assembly of nanoparticles on scaffolds derived from block copolymers

被引:38
|
作者
Darling, S. B. [1 ]
机构
[1] Argonne Natl Lab, Ctr Nanoscale Mat, Argonne, IL 60439 USA
关键词
atomic force microscopy; electron microscopy; self-assembly; hierarchical assembly; block copolymers; nanostructures; cadmium selenide; iron platinum;
D O I
10.1016/j.susc.2006.11.052
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
Lithographically patterned substrates can direct the self-assembly of block copolymer films into aligned structures that, in turn, template the self-organization of colloidal nanoparticles. Deposition on pristine diblock copolymer films does not lead to reproducible selective decoration, but films modified to have nanoscale corrugation act as scaffolds for highly selective nanoparticle adsorption. The mechanism for this selectivity relies on the lateral forces inherent to spin casting to remove all of the nanoparticle suspension not confined within the nanoscopic trenches. This technique does not rely on interactions between the surfactant capping molecules and the polymer and is therefore general to a wide class of nanoparticle materials. Prospects to obtain long-range ordering and associated potential applications are discussed. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:2555 / 2561
页数:7
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