论文标题
光活性列明体的光学机械耦合
Photomechanical coupling in photoactive nematic elastomers
论文作者
论文摘要
光活性列弹性体是柔软的橡胶固体,在照明时会变形。它们是通过将偶氮苯(如偶氮苯)中的光活性分子掺入列液液晶体弹性体中制成的。自2001年最初的示威活动以来,它对许多最近对周期性和屈曲行为的研究引起了人们的兴趣。然而,在没有机械载荷的情况下,开发的理论模型集中在描述特定变形模式(例如,光束弯曲和单轴收缩),只有对机械应力和光诱导的变形之间相互作用的关注只有有限的关注。本文在光照明和机械应力下探讨了光活性的弹性弹性体中的光机械耦合。我们从Corbett和Warner开发的自由能建立的连续框架开始(Phys。Rev。Lett。2006)。机械应力导致与单轴拉伸应力平行的列对齐。在没有机械应力的情况下,在系统达到平衡状态的光态状态下,列表主管倾向于垂直于线性极化光的极化。然而,足够的照明可以通过一阶的近视相变破坏列表,并通过变形伴随着快照。相结合的照明和机械应力会导致稳定性交换,并伴有条纹结构域。最后,应力强度相图显示了一个关键点,这可能是能量转化的关键点。
Photoactive nematic elastomers are soft rubbery solids that undergo deformation when illuminated. They are made by incorporating photoactive molecules like azobenzene into nematic liquid crystal elastomers. Since its initial demonstration in 2001, it has received increasing interest with many recent studies of periodic and buckling behavior. However, theoretical models developed have focused on describing specific deformation modes (e.g., beam bending and uniaxial contraction) in the absence of mechanical loads, with only limited attention to the interplay between mechanical stress and light-induced deformation. This paper explores photomechanical coupling in a photoactive nematic elastomer under both light illumination and mechanical stress. We begin with a continuum framework built on the free energy developed by Corbett and Warner (Phys. Rev. Lett. 2006). Mechanical stress leads to nematic alignment parallel to a uniaxial tensile stress. In the absence of mechanical stress, in the photo-stationary state where the system reaches equilibrium, the nematic director tends to align perpendicular to the polarization of a linearly polarized light. However, sufficient illumination can destroy nematic order through a first-order nematic-isotropic phase transition which is accompanied by a snap through deformation. Combined illumination and mechanical stress can lead to an exchange of stability accompanied by stripe domains. Finally, the stress-intensity phase diagram shows a critical point that may be of interest for energy conversion.