Oriented mesoporous organosilicate thin films

被引:135
作者
Freer, EM [1 ]
Krupp, LE [1 ]
Hinsberg, WD [1 ]
Rice, PM [1 ]
Hedrick, JL [1 ]
Cha, JN [1 ]
Miller, RD [1 ]
Kim, HC [1 ]
机构
[1] IBM Corp, Almaden Res Ctr, Div Res, San Jose, CA 95120 USA
关键词
D O I
10.1021/nl051517h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Coassemblies of block copolymers and inorganic precursors offer a path to ordered inorganic nanostructures. In thin films, these materials combined with domain alignment provide highly robust nanoscopic templates. We report a simple path to control the morphology, scaling, and orientation of ordered mesopores in organosilicate thin films through the coassembly of a diblock copolymer, poly(styrene-b-ethylene oxide) (PS-b-PEO), and an oligomeric organosilicate precursor that is selectively miscible with PEO. Continuous films containing cylindrical or spherical pores are generated by varying the mixing composition of symmetric PS-b-PEO and an organosilicate precursor. Tuning interfacial energy at both air/film and film/substrate interfaces allows the control of cylindrical pore orientation normal to the supported film surfaces. Our method provides well-ordered mesoporous structures within organosilicate thin films that find broad applications as highly stable nanotemplates.
引用
收藏
页码:2014 / 2018
页数:5
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