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6MNEP: a molecular cation with large hyperpolarizability and promise for nonlinear optical applications

机译:6MEP:具有大的超极化性和非线性光学应用的承诺的分子阳离子

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摘要

Molecular organic crystals are strategically designed for nonlinear optical applications using push-pull chromophores as the core feature. In this approach, electron-donating and accepting groups are connected through a pi-conjugated bridge to obtain planar molecules with high hyperpolarizability. However, the non-centrosymmetric packing that is required for nonlinear optical (NLO) applications is a critical challenge that must be addressed to design useful materials. In this article, we present the new organic cation 6MNEP that shows a large hyperpolarizability and can be crystallized in ideal non-centrosymmetric structures for NLO applications, when paired with T and 4NBS anions. The 6MNEP cation was obtained by extending the conjugation length of already existing chromophores. We compare the 6MNEP crystals with other crystals that also have cations with extended conjugation lengths, but result in centrosymmetric crystal structures. Using the effective hyperpolarizability, we found 6MNEP-T and 6MNEP-4NBS to have 1.6 to 2.5 times larger macroscopic nonlinearities than benchmark NLO organic crystals. Additionally, the significantly lower absorption wavelength compared with other state-of-the-art crystals make 6MNEP-T and 6MNEP-4NBS promising materials for NLO applications like intense terahertz generation.
机译:分子有机晶体是用于使用推拉式发色团作为核心特征的非线性光学应用的策略性设计。在这种方法中,通过PI-共轭桥连接电子提供和接受基团以获得具有高超极化性的平面分子。然而,非线性光学(NLO)应用所需的非亚离子微量填料是必须寻址设计有用材料的关键挑战。在本文中,我们介绍了新的有机阳离子6MNEP,其显示出大的超极化性,并且当与T和4NBS阴离子配对时,可以在NLO应用的理想非CentroSmmetric结构中结晶。通过延长已经存在的发色团的共轭长度来获得6mnep阳离子。我们将6mnep晶体与其他晶体进行比较,该晶体也具有延伸的共轭长度的阳离子,但导致亚光铬晶体结构。使用有效的超极化性,我们发现6mnep-t和6mnep-4nbs,比基准NLO有机晶体更大的宏观非线性具有1.6至2.5倍。另外,与其他最先进的晶体相比的吸收波长显着较低,使6mnep-t和6mnep-4nbs用于NLO应用,如强烈的太赫兹一代。

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