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

An indented nanostructure was formed on the surface of azobenzene-functiona lized polyurethane thin films by the induced migration of polymer chains us ing the optical near field generated around polystyrene (PS) spheres. The P S 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 p rocess, and the films were then exposed to a linearly polarized Ar+ laser a t 488 nm. A hexagonal array of indentations reflecting the original geometr y and arrangement of the spheres was observed on the polyurethane surface b y atomic force microscopy. The indented structure that was formed had a res olution of similar to 95 nm. This structure was stable at room temperature and could be erased by heating the films above their glass transition tempe rature (T,). The modification depth and diameter of the dents formed depend ed 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 opti cal lens effect they created, and the irradiation onto spheres of greater t han 505 nm diameter with linearly polarized light induced an anisotropic mo dification on the surface of the polymer films. The thickness of the polyme r film significantly affected the modification depth of the dent. We prepar ed three different kinds of photoresponsive polyurethane, each containing a slightly different azobenzene moiety. Although these polymers all had virt ually the same molecular weight, Tg, and absorptivity at the wavelength of the irradiated light, the modified depth of the dent observed for each of t he films was very different. Furthermore, a dependence between the irradiat ed 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.