Self-assembly in the synthesis of ceramic materials and composites

被引:100
作者
Liu, J
Kim, A
Wang, LQ
Palmer, BJ
Chen, YL
Bruinsma, P
Bunker, BC
Exarhos, GJ
Graff, GL
Rieke, PC
Fryxell, GE
Virden, JW
Tarasevich, BJ
Chick, LA
机构
[1] Pac. Northwest National Laboratory, Richland
关键词
self-assembly; nanocomposites; mesoporous; surfactant; biomimetic;
D O I
10.1016/S0001-8686(96)00309-0
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 self-assembly process provides an effective and environmentally benign method for synthesizing novel ceramic and composite materials. Three different approaches are discussed in this article: (1) self-assembly of colloidal crystals, (2) self-assembled monolayers, and (3) three-dimensional self-assembly with amphiphilic molecules. The self-assembly of colloidal crystals allows the synthesis of periodic optical devices and quantum dots from simple monodispersed particles. Self-assembled monolayers provide a molecular template to control the nucleation and growth of ceramic thin films. The emphasis of this paper will be on the self-assembly process with amphiphilic molecules, which represents the latest breakthrough in the design and synthesis of tailored nanoscale materials and composites. In the past few years, self-assembled materials have become a very active research area. This article illustrates how the basic principles of self-assembly can be applied in the synthesis of ceramic materials and discusses the role of various inter-molecular and into-particular forces.
引用
收藏
页码:131 / 180
页数:50
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