Directed Self-Assembly of Asymmetric Block Copolymers in Thin Films Driven by Uniaxially Aligned Topographic Patterns

被引:17
|
作者
Lee, Dong-Eun [1 ]
Ryu, Jaegeon [2 ]
Hong, Dongki [2 ]
Park, Soojin [2 ]
Lee, Dong Hyun [1 ]
Russell, Thomas P. [3 ]
机构
[1] Dankook Univ, Dept Polymer Sci & Engn, 152 Jukjeon Ro, Yongin 16890, Gyeonggi Do, South Korea
[2] UNIST, Sch Energy & Chem Engn, Dept Energy Engn, Ulsan 44919, South Korea
[3] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
基金
新加坡国家研究基金会;
关键词
block copolymer; directed self-assembly; thin films; solvent-annealing; topographic patterns; FACETED SURFACES; FIELD ALIGNMENT; ORIENTED GROWTH; ARRAYS; POLY(TETRAFLUOROETHYLENE); NANOPARTICLES; ORIENTATION; PLASMA; POLYDIMETHYLSILOXANE; FABRICATION;
D O I
10.1021/acsnano.7b08226
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present a simple, versatile approach to generate highly ordered nanostructures of block copolymers (BCPs) using rubbed surfaces. A block of poly(tetrafluoroethylene) (PTFE) was dragged across a flat substrate surface above the melting point of PTFE transferring a highly aligned PTFE topographic pattern to the substrate. Si wafer, glass, and polyimide films were used as substrates. Thin films of cylinder-forming asymmetric polystyrene-b/ock-poly(2-vinylpyridine) copolymers (S2VPs) were solvent annealed on the surfaces having the transferred surface pattern to induce their directed self-assembly. Cylinders of P2VP oriented normal to the surface are markedly aligned along the rubbing direction and used as templates to generate extremely uniform arrays of various metallic nanoparticles of gold, silver, and platinum over a large area.
引用
收藏
页码:1642 / 1649
页数:15
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