Controlling polymer-surface interactions with random copolymer brushes

被引:1273
作者
Mansky, P
Liu, Y
Huang, E
Russell, TP
Hawker, CJ
机构
[1] UNIV MASSACHUSETTS, DEPT POLYMER SCI & ENGN, NATL CTR POLYMER RES, AMHERST, MA 01003 USA
[2] IBM CORP, ALMADEN RES CTR, SAN JOSE, CA 95120 USA
关键词
D O I
10.1126/science.275.5305.1458
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
A simple technique for precisely controlling the interfacial energies and wetting behavior of polymers in contact with solid surfaces is described, End-functionalized statistical random copolymers of styrene and methylmethacrylate were synthesized, with the styrene fraction f varying from 0 to 1, and were end-grafted onto silicon substrates to create random copolymer brushes about 5 nanometers thick, For f < 0.7, polystyrene (PS) films (20 nanometers thick) rapidly dewet from the brushes when heated well above the glass transition temperature. The contact angle of the resulting polymer droplets increased monotonically with decreasing f. Similar behavior was observed for poly(methylmethacrylate) (PMMA) films but with an opposite dependence on f. The interfacial energies of the random copolymer brushes with PS and PMMA were equal when f was about 0.6. Thus, precise control of the relative surface affinities of PS and PMMA was possible, demonstrating a way to manipulate polymer-surface interactions.
引用
收藏
页码:1458 / 1460
页数:3
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