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胆甾相液晶中的滑动平面锚定和粘性表面扭矩。

Sliding planar anchoring and viscous surface torque in a cholesteric liquid crystal.

作者信息

Oswald Patrick, Dequidt Alain, Zywociński Andrzej

机构信息

Université de Lyon, Laboratoire de Physique, Ecole Normale Supérieure de Lyon, CNRS, 46 Allée d'Italie, 69364 Lyon, France.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2008 Jun;77(6 Pt 1):061703. doi: 10.1103/PhysRevE.77.061703. Epub 2008 Jun 6.

Abstract

We propose a surface treatment allowing one to obtain a sliding planar anchoring of nematic (or cholesteric) liquid crystals. It consists of depositing a thin layer of the polymercaptan hardener of an epoxy resin on an isotropic substrate (bare or ITO-coated glass plates). Microscopic observations of defect annihilations and capacitance measurements show that the molecules align parallel to the surface and slide viscously on it when they change orientation, which implies a zero (or extremely small) azimuthal anchoring energy. In contrast, the zenithal anchoring energy W theta is found to be larger than 3 x 10(-5)J/m2. We also measured the liquid crystal rotational surface viscosity gammaS by a thermo-optical method using the large temperature variation of the pitch of a compensated cholesteric mixture. We found that the sliding length gammaS/gamma1 (where gamma1 is the bulk rotational viscosity) is very large in comparison with the length of a liquid crystal molecule. This result is explained by a simple model which takes into account the diffusion of the liquid crystal within the polymer layer.

摘要

我们提出一种表面处理方法,可实现向列相(或胆甾相)液晶的滑动平面锚定。该方法是在各向同性衬底(裸玻璃板或涂有ITO的玻璃板)上沉积一层环氧树脂的聚合物硫醇固化剂薄层。对缺陷湮灭的显微镜观察和电容测量表明,分子与表面平行排列,并且在改变取向时在表面上粘性滑动,这意味着方位角锚定能为零(或极小)。相比之下,发现天顶角锚定能Wθ大于3×10^(-5)J/m²。我们还通过热光学方法,利用补偿胆甾相混合物螺距的大幅温度变化,测量了液晶的旋转表面粘度γS。我们发现,与液晶分子的长度相比,滑动长度γS/γ1(其中γ1是本体旋转粘度)非常大。这个结果由一个简单的模型解释,该模型考虑了液晶在聚合物层内的扩散。

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