Topographical nanostructure patterning on the surface of a thin film of polyurethane containing azobenzene moiety using the optical near field around polystyrene spheres

被引:37
作者
Hasegawa, M
Ikawa, T
Tsuchimori, M
Watanabe, O [1 ]
Kawata, Y
机构
[1] Toyota Cent Res & Dev Labs Inc, Nagakute, Aichi 4801192, Japan
[2] Shizuoka Univ, Fac Engn, Hamamatsu, Shizuoka 4328561, Japan
关键词
D O I
10.1021/ma0102870
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
An indented nanostructure was formed on the surface of azobenzene-functionalized polyurethane thin films by the induced migration of polymer chains using the optical near field generated around polystyrene (PS) spheres. The PS spheres, which had a diameter ranging from 98 to 990 nm, were arranged on the surface of a photoresponsive polymer film using a self, organization process, and the films were then exposed to a linearly polarized Ar+ laser at 488 nm. A hexagonal array of indentations reflecting the original geometry and arrangement of the spheres was observed on the polyurethane surface by atomic force microscopy. The indented structure that was formed had a resolution of similar to 95 nm. This structure was stable at room temperature and could be erased by heating the films above their glass transition temperature (T,). The modification depth and diameter of the dents formed depended on the size of the original PS spheres. In particular, deeper dents were formed by using PS spheres with a diameter of over 505 nm, due to the optical lens effect they created, and the irradiation onto spheres of greater than 505 nm diameter with linearly polarized light induced an anisotropic modification on the surface of the polymer films. The thickness of the polymer film significantly affected the modification depth of the dent. We prepared three different kinds of photoresponsive polyurethane, each containing a slightly different azobenzene moiety. Although these polymers all had virtually the same molecular weight, Tg, and absorptivity at the wavelength of the irradiated light, the modified depth of the dent observed for each of the films was very different. Furthermore, a dependence between the irradiated light intensity and the size of dent achievable was observed, which was due to the difference in the trans-cis-trans isomerization behavior of the azobenzene moiety.
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页码:7471 / 7476
页数:6
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