Photoresponsive monolayers on water and solid surfaces

Takahiro Seki, Hidehiko Sekizawa, Keisuke Tanaka, Yoko Matsuzawa, Kunihiro Ichimura
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引用次数: 5

Abstract

Organic photochromic units and molecules can be regarded as light-driven nano molecular machines. Once such molecules are aligned at a surface, the supramolecular organization provides an efficient macroscopic mechanical response in a collective way. Amphiphilic polymers having an azobenzene (Az) side chain are the favorable materials for observation of such effects since they show marked photomechanical response with essentially full reversibility. An in situ Brewster angle microscopic observation showed marked morphological and rheological photoinduced changes in the molecular films. Moreover, we have newly found that the identical photosensitive molecular film transferred on to a solid mica surface shows large morphological changes under highly humid conditions as proven by atomic force microscopy (AFM). It is supposed that the molecular film is driven in the same mechanism both on water and water-adsorbed mica surfaces. These microscopic observations provide new insights of the photomechanical response in photochromic monolayers.

水和固体表面的光响应单层膜
有机光致变色单元和分子可以看作是光驱动的纳米分子机器。一旦这些分子排列在表面上,超分子组织就以集体的方式提供了有效的宏观机械响应。具有偶氮苯(Az)侧链的两亲性聚合物是观察这种效应的有利材料,因为它们表现出明显的光力学响应,基本上具有完全的可逆性。原位布鲁斯特角显微镜观察显示,分子膜在光诱导下发生了明显的形态和流变变化。此外,我们最近发现,原子力显微镜(AFM)证明,在高度潮湿的条件下,转移到固体云母表面的相同光敏分子膜显示出巨大的形态变化。推测分子膜在水和水吸附云母表面的驱动机理相同。这些显微观察为光致变色单层膜的光力学响应提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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