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在诱导的 Smectic-C_{A} 膜表面上的一个简单的刃型位错上的定位。

Director anchoring on a simple edge dislocation at the surface of induced smectic-C_{A} films.

机构信息

Université de Strasbourg, CNRS, Institut de Physique et Chimie des Matériaux de Strasbourg, UMR 7504, F- 67000 Strasbourg, France.

出版信息

Phys Rev E. 2023 May;107(5-1):054702. doi: 10.1103/PhysRevE.107.054702.

Abstract

We present a detailed analysis of c-director anchoring measurements on simple edge dislocations at the surface of smectic-C_{A} films (steps). Indications show that the c-director anchoring on the dislocations originates from a local and partial melting of the dislocation core that depends on the anchoring angle. The SmC_{A} films are induced on isotropic puddles of 1-(methyl)-heptyl-terephthalylidene-bis-amino cinnamate molecules by the surface field, while the dislocations are located at the isotropic-smectic interface. The experimental setup is based on the connection of a three-dimensional smectic film sandwiched between a one-dimensional edge dislocation on its lower surface, and a two-dimensional surface polarization spread over the upper surface. Applying an electric field produces a torque that balances the anchoring torque of the dislocation. The film distortion that results is measured under a polarizing microscope. Exact calculations on these data, anchoring torque versus director angle, yield the anchoring properties of the dislocation. A specificity of our sandwich configuration is to improve the measurement quality by a factor of N^{3/2}∼600, where N=72 is the number of smectic layers in the film. We fit a second-order Fourier series on the torque-anchoring angle data, which has the advantage of converging uniformly over the entire anchoring angle range, i.e., over more than 70^{∘}. The two corresponding Fourier coefficients, k_{a1}^{F2} and k_{a2}^{F2}, are anchoring parameters that generalize the usual anchoring coefficient. When changing the electric field E, the anchoring state evolves along paths in a torque-anchoring angle diagram. Two cases occur depending on the angle α_{∞} of E relative to the unit vector S, perpendicular to the dislocation and parallel to the film. When α_{∞}<130^{∘}, the operating point Q that represents the anchoring state in the diagram follows reversible and "at-equilibrium" paths. Its free displacement velocity is infinitely slow, so that we have to push it with electric torque steps smaller than the experimental error bar δΓ∼10^{-14}N. On the other hand, for α_{∞}>130^{∘}, Q describes a hysteresis loop similar to the usually encountered ones in solids. This loop connects two states that exhibit broken and nonbroken anchorings, respectively. The paths that join them in an out-of-equilibrium process are irreversible and dissipative. When coming back to a nonbroken anchoring state, both the dislocation and smectic film spontaneously heal back in the very same state they were before the anchoring broke. The process does not produce any erosion thanks to their liquid nature, including at the microscopic scale. The energy that is dissipated on these paths is roughly estimated in terms of the c-director rotational viscosity. Similarly, we can evaluate the maximum time of flight along the dissipative paths to be of the order of a few seconds, which is consistent with qualitative observations. In contrast, the paths located inside each domain of these anchoring states are reversible and can be followed in an "at equilibrium" manner all along. This analysis should provide a basis for understanding the structure of multiple edge dislocations in terms of parallel simple edge dislocations interacting with each other through pseudo-Casimir forces arising from c-director thermodynamic fluctuations between them.

摘要

我们对 SmC_{A} 薄膜(台阶)表面简单位错的 c 向锚定测量进行了详细分析。结果表明,位错上的 c 向锚定源于位错核的局部和部分熔化,这取决于锚定角。SmC_{A} 薄膜是通过表面场在各向同性的 1-(甲基)庚基对苯二甲酰基-双-氨基肉桂酸分子的液滴中诱导的,而位错位于各向同性-向列界面处。实验装置基于夹在其下表面一维位错之间的三维向列膜与上表面二维表面极化的连接。施加电场会产生一个扭矩,该扭矩与位错的锚定扭矩平衡。在偏光显微镜下测量由此产生的膜变形。对位错上这些数据(锚定扭矩与指向角)进行精确计算,可得出位错的锚定特性。我们三明治结构的一个特点是通过因子 N^{3/2}∼600 提高测量质量,其中 N=72 是膜中的向列层的数量。我们对位错扭矩-锚定角数据进行了二阶傅里叶级数拟合,这具有在整个锚定角范围内均匀收敛的优点,即在超过 70^{∘}的范围内。两个对应的傅里叶系数 k_{a1}^{F2}和 k_{a2}^{F2}是锚定参数,它们概括了通常的锚定系数。当改变电场 E 时,锚定状态沿着扭矩-锚定角图中的路径演变。根据 E 相对于垂直于位错且平行于膜的单位向量 S 的角度 α_{∞},会发生两种情况。当 α_{∞}<130^{∘}时,代表图中锚定状态的工作点 Q 遵循可逆且“处于平衡”的路径。它的自由位移速度非常缓慢,因此我们必须使用小于实验误差条 δΓ∼10^{-14}N 的电扭矩步来推动它。另一方面,当 α_{∞}>130^{∘}时,Q 描述了一个类似于在固体中通常遇到的滞后环。该环连接了分别表现出断裂和非断裂锚定的两个状态。在非平衡过程中将它们连接起来的路径是不可逆的和耗散的。当回到非断裂锚定状态时,位错和向列膜都会自发地恢复到它们在锚定断裂之前的状态。由于它们的液态性质,包括在微观尺度上,不会产生任何侵蚀。根据 c 向指向旋转粘度,我们可以大致估计这些路径上耗散的能量。同样,我们可以评估沿着耗散路径的最大飞行时间,大约为几秒钟,这与定性观察一致。相比之下,这些锚定状态的每个区域内的路径是可逆的,可以一直以“平衡”方式遵循。这种分析应该为理解多个边缘位错的结构提供基础,这些位错可以通过它们之间的伪 Casimir 力相互作用,这些伪 Casimir 力来自它们之间的 c 向热力学波动产生的平行简单边缘位错。

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