Topographical Nanostructure Patterning on the Surface of a Thin Film of Polyurethane Containing Azobenzene Moiety Using the Optical Near Field around Polystyrene Spheres

Abstract

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 ∼95 nm. This structure was stable at room temperature and could be erased by heating the films above their glass transition temperature (T g). 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, T g, 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.

Electrochemical fluorescence switching properties of conjugated polymers composed of triphenylamine, fluorene, and cyclic urea moieties

“…Polyurethanes and polyureas (PUs) form an important family of industrial polymers that have been widely used due to their good properties such as elasticity, flexibility, thermal stability, and excellent chemical resistance 52–58. In addition, PU conducting polymers have recently been developed59–61 and applications of PUs on PLED have been reported.…”

Photochromic polyacylsemicarbazides based on azobenzene containing dihydrazide

“…Azo‐containing polymer systems include polymer matrices doped with azo dyes4, liquid crystalline azo polymers5, 6, Langmuir–Blodgett films7, 8 and amorphous azo polymers9 in which the azo benzene groups are attached to the polymer main chain directly or as side groups. A large number of polyamides10–12 and polyurethanes13–20 with azobenzene groups either in the main chain or as pendant groups have been studied.…”

Low-Cost and Easy-to-Use “on-Chip ELISA” for Developing Health-Promoting Foods

“…We found that the surface of a polymer containing an azobenzene (azopolymer) can transform along with the surface of an attached object by means of irradiating blue light (Kawata et al 1999;Ikawa et al 2000Ikawa et al , 2001Ikawa et al , 2006Hasegawa et al 2001). Figure 13.1 shows the chemical structure of a typical azopolymer.…”