偶氮苯非晶聚合物光致取向的可见光、红外和拉曼光谱研究

F. L. Labarthet, T. Buffeteau, C. Sourisseau
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引用次数: 0

摘要

近年来,含偶氮染料的聚合物体系在光子模式光存储、光信息转导、电子电导率的光开关等光功能应用领域得到了广泛的研究。这种掺杂或功能化系统的主要兴趣是由于它们在偏振光照射时的二色性和双折射特性。这种效应是相对于N=N双键可逆的"反↔顺"光异构化的结果,它导致光致变色实体的取向重新分布。在这方面,Dumont等人1已经报道了一个简单的三层理论模型的基础,以解释偶氮分子在光异构化循环中的重定向机制。因此,我们报告了通过原位时间依赖可见光和偏振调制FTIR光谱测量对dr1 -偶氮染料在聚合物基体(PMMA)中光异构诱导的重定向动力学研究的结果。最后是利用全息法获得的高效衍射图样的生成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Study of photoinduced orientation of azobenzene amorphous polymer by Visible, FTIR and Raman spectroscopy
Azo-dye containing polymeric systems have been a subject of intensive research in the last few years in the areas of photofunctional applications such as photon mode optical memories, transducing optical information, photoswitching of electron conductivity. The main interest of such doped or functionalized systems is due to their dichroic and birefringent properties when they are illuminated by a polarized light. Such an effect is a consequence of the reversible “trans↔cis” photoisomerisation with respect to the N=N double bond which causes a redistribution in the orientation of photochromic entities. In this respect, Dumont et al.1 have already reported the basis of a simple three-level theoretical model in order to explain the reorientation mechanisms of the azo molecules within a photoisomerisation cycle. Hereafter we thus report the results of a dynamical study of the photoisomerisation-induced reorientation of DR1-azo-dye in a polymer matrix (PMMA) by in-situ time dependent Visible and polarisation modulation FTIR spectroscopy measurements. The last part concerns the generation of high-efficiency diffraction patterns obtained by holographic way.
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