Block copolymer assembly via kinetic control

被引:919
作者
Cui, Honggang
Chen, Zhiyun
Zhong, Sheng
Wooley, Karen L. [1 ]
Pochan, Darrin J.
机构
[1] Washington Univ, Ctr Mat Innovat, Dept Chem, St Louis, MO 63130 USA
[2] Washington Univ, Ctr Mat Innovat, Dept Radiol, St Louis, MO 63130 USA
[3] Univ Delaware, Dept Mat Sci & Engn, Newark, DE 19716 USA
[4] Univ Delaware, Delaware Biotechnol Inst, Newark, DE 19716 USA
关键词
D O I
10.1126/science.1141768
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
Block copolymers consist of two or more chemically different polymer segments, or blocks, connected by a covalent linkage. In solution, amphiphilic blocks can self-assemble as a result of energetic repulsion effects between blocks. The degree of repulsion, the lengths of the block segments, and the selectivity of the solvent primarily control the resultant assembled morphology. In an ideal situation, one would like to be able to alter the morphology that forms without having to change the chemistry of the block copolymer. Through the kinetic manipulation of charged, amphiphilic block copolymers in solution, we are able to generate different nanoscale structures with simple block copolymer chemistry. The technique relies on divalent organic counter ions and solvent mixtures to drive the organization of the block copolymers down specific pathways into complex one-dimensional structures. Block copolymers are increasingly used as templating materials; thus, the ability to control the formation of specific patterns and structures is of growing interest and applicability.
引用
收藏
页码:647 / 650
页数:4
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