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光致液晶性。

Light-induced liquid crystallinity.

机构信息

Alpha Micron Inc., Kent, Ohio 44240, USA.

出版信息

Nature. 2012 May 16;485(7398):347-9. doi: 10.1038/nature11122.

Abstract

Liquid crystals are traditionally classified as thermotropic, lyotropic or polymeric, based on the stimulus that governs the organization and order of the molecular system. The most widely known and applied class of liquid crystals are a subset of thermotropic liquid crystals known as calamitic, in which adding heat can result in phase transitions from or into the nematic, cholesteric and smectic mesophases. Photoresponsive liquid-crystal materials and mixtures can undergo isothermal phase transitions if light affects the order parameter of the system within a mesophase sufficiently. In nearly all previous examinations, light exposure of photoresponsive liquid-crystal materials and mixtures resulted in order-decreasing photo-induced isothermal phase transitions. Under specialized conditions, an increase in order with light exposure has been reported, despite the tendency of the photoresponsive liquid-crystal system to reduce order in the exposed state. A direct, photo-induced transition from the isotropic to the nematic phase has been observed in a mixture of spiropyran molecules and a nematic liquid crystal. Here we report a class of naphthopyran-based materials that exhibit photo-induced conformational changes in molecular structure capable of yielding order-increasing phase transitions. Appropriate functionalization of the naphthopyran molecules leads to an exceedingly large order parameter in the open form, which results in a clear to strongly absorbing dichroic state. The increase in order with light exposure has profound implications in optics, photonics, lasing and displays and will merit further consideration for applications in solar energy harvesting. The large, photo-induced dichroism exhibited by the material system has been long sought in ophthalmic applications such as photochromic and polarized variable transmission sunglasses.

摘要

液晶传统上根据控制分子系统的组织和秩序的刺激物分为热致、溶致或聚合型。最广泛知晓和应用的液晶类别是热致液晶中的一类,称为棒状液晶,其中添加热量会导致从向列相、胆甾相和近晶相等中间相或进入中间相的相转变。光响应液晶材料和混合物如果光在中间相内足够影响系统的有序参数,则可以经历等温相变。在几乎所有以前的检查中,光响应液晶材料和混合物的光暴露导致有序降低的光诱导等温相变。尽管光响应液晶系统在暴露状态下趋于降低有序,但在特殊条件下,已报道了光暴露时有序增加的报道。已经在螺吡喃分子和向列相液晶的混合物中观察到从各向同性相到向列相的直接光诱导转变。在这里,我们报告了一类基于萘并吡喃的材料,它们表现出光诱导分子结构构象变化,能够产生有序增加的相变。萘并吡喃分子的适当官能化导致开式构象中的非常大的有序参数,从而产生清晰至强烈吸收的二色性状态。光暴露时有序的增加在光学、光子学、激光和显示器方面具有深远的意义,并且将值得进一步考虑用于太阳能收集的应用。在眼科应用中,例如光致变色和偏振可变透射太阳镜,一直以来都在寻找材料系统所具有的大、光诱导二色性。

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