Enabling nanotechnology with self assembled block copolymer patterns

被引:1367
作者
Park, C
Yoon, J
Thomas, EL
机构
[1] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[2] Yonsei Univ, Dept Met Syst Engn, Seoul 120749, South Korea
[3] MIT, Inst Soldier Nanotechnol, Cambridge, MA 02139 USA
关键词
block copolymers; self-assembly; nanostructures;
D O I
10.1016/j.polymer.2003.08.011
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Block copolymers (BCPs) have received great attention for the past 40 years but only within the past decade have they been seriously considered for nanotechnological applications. Their applicability to nanotechnology stems from the scale of the microdomains and the convenient tunability of size, shape, and periodicity afforded by changing their molecular parameters. The use of the tensorial physical properties of BCPs in such areas as transport, mechanical, electrical, and optical properties will provide substantial benefits in the future. In this review article, we first focus on the current efforts to utilize BCPs in nanotechnologies including nanostructured membranes, BCP templates for narroparticle synthesis, photonic crystals, and high-density information storage media. In order to realize these applications, control over microdomain spatial and orientational order is paramount. This article reviews various methods to control BCP microdomain structures in the bulk state as well as in thin films. A variety of biases such as mechanical flow fields, electric fields, temperature gradients, and surface interactions can manipulate the microstructures of BCPs. A particular emphasis is made on two approaches, epitaxy and graphoepitaxy, and their combinations. Manipulation of BCP microdomain structures employing multiple external fields promises realization of many potential nanotechnological applications. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6725 / 6760
页数:36
相关论文
共 319 条
[11]   Confined thin film diblock copolymer in the presence of an electric field [J].
Ashok, B ;
Muthukumar, M ;
Russell, TP .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (03) :1559-1564
[12]  
BALL P, 1997, BIOMATERIALS, pCH4
[13]   Thermoreversible, epitaxial fcc ⇆ bcc transitions in block copolymer solutions -: art. no. 215505 [J].
Bang, J ;
Lodge, TP ;
Wang, XH ;
Brinker, KL ;
Burghardt, WR .
PHYSICAL REVIEW LETTERS, 2002, 89 (21)
[14]   Block copolymers - Designer soft materials [J].
Bates, FS ;
Fredrickson, GH .
PHYSICS TODAY, 1999, 52 (02) :32-38
[15]   Integration of self-assembled diblock copolymers for semiconductor capacitor fabrication [J].
Black, CT ;
Guarini, KW ;
Milkove, KR ;
Baker, SM ;
Russell, TP ;
Tuominen, MT .
APPLIED PHYSICS LETTERS, 2001, 79 (03) :409-411
[16]   Device applications of side-chain ferroelectric liquid crystalline polymer films [J].
Blackwood, KM .
SCIENCE, 1996, 273 (5277) :909-912
[17]   Self-assembly of nanoparticles into structured spherical and network aggregates [J].
Boal, AK ;
Ilhan, F ;
DeRouchey, JE ;
Thurn-Albrecht, T ;
Russell, TP ;
Rotello, VM .
NATURE, 2000, 404 (6779) :746-748
[18]  
Bockstaller M, 2001, ADV MATER, V13, P1783, DOI 10.1002/1521-4095(200112)13:23<1783::AID-ADMA1783>3.0.CO
[19]  
2-X
[20]   Size-selective organization of enthalpic compatibilized nanocrystals in ternary block copolymer/particle mixtures [J].
Bockstaller, MR ;
Lapetnikov, Y ;
Margel, S ;
Thomas, EL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (18) :5276-5277