Apertureless near-field vibrational imaging of block-copolymer nanostructures with ultrahigh spatial resolution

被引:82
作者
Raschke, MB [1 ]
Molina, L
Elsaesser, T
Kim, DH
Knoll, W
Hinrichs, K
机构
[1] Max Born Inst Nichtlineare Opt & Kurzzeitspektros, D-12489 Berlin, Germany
[2] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[3] Inst Analyt Sci, D-12489 Berlin, Germany
关键词
block copolymers; IR spectroscopy; nanostructures; scanning probe microscopy; vibrational imaging;
D O I
10.1002/cphc.200500218
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nonodomains formed by microphase separation in thin films of the diblock copolymers poly(styrene-b-2-vinylpyridine) (PS-b-P2VP) and poly(styrene-b-ethyleneoxide) (PS-b-PEO) were imaged by means of infrared scattering-type near-field microscopy. When probing at 3.39 mu m (2950 cm(-1)), contrast is obtained due to spectral differences between the C-H stretching vibrational resonances of the respective polymer constituents. An all-optical spatial resolution better than 10 nm was achieved, which corresponds to a sensitivity of just several thousand C-H groups facilitated by the local-field enhancement at the sharp metallic probe tips. The results demonstrate that infrared spectroscopy with access to intramolecular dimensions is within reach.
引用
收藏
页码:2197 / 2203
页数:7
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