Institute for Molecular Engineering, The University of Chicago, Chicago, IL, 60637, USA.
Department of Physics and Soft Materials Research Center, University of Colorado, Boulder, CO, 80309, USA.
Nat Commun. 2019 Mar 1;10(1):1000. doi: 10.1038/s41467-019-08645-9.
The defect structure associated with a colloid in a nematic liquid crystal is dictated by molecular orientation at the colloid surface. Perpendicular or parallel orientations to the surface lead to dipole-like or quadrupole-like defect structures. However, the so-called elastic hexadecapole discovered recently, has been assumed to result from a conic anchoring condition. In order to understand it at a fundamental level, a model for this anchoring is introduced here in the context of a Landau-de Gennes free energy functional. We investigate the evolution of defect configurations, as well as colloidal interactions, by tuning the preferred tilt angle (θ). The model predicts an elastic dipole whose stability decreases as θ increases, along with a dipole-hexadecapole transformation, which are confirmed by our experimental observations. Taken together, our results suggest that previously unanticipated avenues may exist for design of self-assembled structures via control of tilt angle.
与各向异性液晶中的胶粒相关的缺陷结构由胶粒表面的分子取向决定。垂直或平行于表面的取向导致偶极子或四极子样的缺陷结构。然而,最近发现的所谓弹性十六极子,被认为是由圆锥锚定条件引起的。为了从根本上理解它,我们在这里引入了一个用于兰道-德加纳斯自由能泛函的这种锚定的模型。我们通过调整优选倾斜角(θ)来研究缺陷构型和胶体相互作用的演化。该模型预测了一个弹性偶极子,其稳定性随着θ的增加而降低,同时还预测了一个偶极子-十六极子的转变,这通过我们的实验观察得到了证实。总的来说,我们的结果表明,通过控制倾斜角,可能存在以前未预料到的途径来设计自组装结构。