一种折叠主链NLO聚合物:光学性质和极化稳定性

W. Herman, L. Hayden, S. Brower, G. Lindsay, J. Stenger-Smith, R. Henry
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摘要

非线性光学(NLO)有机分子(发色团)结合到聚合物中,由于其快速的NLO响应时间、低成本、易于制造和大的非线性二阶电敏感性,在光子学应用中引起了相当大的兴趣,χ(2)。目前研究的一个重点是增强x(2)的热稳定性和时间稳定性,这在NLO聚合物中取决于发色团取向的稳定性。为了获得非零的χ(2),这种方向对于去除反演对称性是必要的,可以通过电场极化实现。2,3电场在接近或高于玻璃化转变温度的温度下施加,以确定发色团的方向,只有在冷却到接近室温时才移除。在热力学非平衡玻璃态下产生的有序的稳定性因聚合物而异。研究发现,发色团与聚合物的化学附着——作为侧链,4-6作为主链的一部分,7 - 8或以交联结构8-10的形式——可以延缓取向顺序的松弛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Folded Mainchain NLO Polymer: Optical Properties and Poling Stability
Nonlinear optical (NLO) organic molecules (chromophores) incorporated into polymers have attracted considerable interest1 for photonics applications due to their fast NLO response time, low cost, ease of fabrication, and large nonlinear second-order electric susceptibility, χ(2). One focus of current research is the enhancement of the thermal and temporal stability of χ(2), which in NLO polymers is dependent on the stability of the Chromophore orientation. This orientation, necessary for the removal of inversion symmetry in order to obtain a nonzero χ(2), can be achieved by electric field poling.2,3 The field is applied at temperatures near or above the glass transition temperature to orient the chromophores and removed only after cooling down to near room temperature. The stability of the resulting order in the thermodynamic nonequilibrium glassy state varies from polymer to polymer. Chemical attachment of the Chromophore to the polymer — as a sidechain,4-6 as part of the main chain,7,8 or in a crosslinked structure8-10 — has been found to retard the relaxation of orientational order.
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