首页> 外文期刊>Macromolecules >Topographical Nanostructure Patterning on the Surface of Thin Film of Polyurethane Containing Azobenzene Moiety Using the Potical Near Field around Polystyrene Spheres
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Topographical Nanostructure Patterning on the Surface of Thin Film of Polyurethane Containing Azobenzene Moiety Using the Potical Near Field around Polystyrene Spheres

机译:利用聚苯乙烯球体附近的垂直近场对含偶氮苯部分的聚氨酯薄膜表面进行形貌纳米构图

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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 photoesponsive polymer film using a self-organization process, and the films were then exposed to a linearly polarized Ar~+ laser at 488 nm. A heagonal 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 (approx)95 nm. This structure was stable at room temperature and could be eraed 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 perticular, 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 azolbenzene 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.
机译:利用在聚苯乙烯(PS)球周围产生的光学近场,通过诱导聚合物链的迁移,在偶氮苯官能化的聚氨酯薄膜的表面上形成了一个凹陷的纳米结构。使用自组织方法将直径为98至990 nm的PS球排列在光敏聚合物膜的表面上,然后将膜暴露于488 nm的线偏振Ar〜+激光中。通过原子力显微镜在聚氨酯表面观察到了一系列凹痕,这些凹痕反映了球的原始几何形状和排列。形成的锯齿状结构的分辨率约为(95 nm)。该结构在室温下稳定,可以通过将膜加热到高于其玻璃化转变温度(T_g)来擦除。形成的凹痕的修改深度和直径取决于原始PS球的大小。在垂直状态下,通过使用直径大于505 nm的PS球形成较深的凹痕,由于它们产生的光学透镜效应,并且用线性偏振光照射到直径大于505 nm的球上会在表面上引起各向异性改性聚合物膜的数量。聚合物膜的厚度显着影响凹痕的改性深度。我们制备了三种不同类型的光敏聚氨酯,每种均包含稍微不同的氮杂苯部分。尽管这些聚合物在照射的光的波长下几乎都具有相同的分子量,T g和吸收率,但是对于每个膜观察到的凹痕的改变深度是非常不同的。此外,观察到所照射的光强度与可达到的凹痕的尺寸之间的依赖性,这是由于偶氮苯部分的反式-顺式-反式异构化行为的差异。

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