【2h】

Entropy driven self-assembly of nonamphiphilic colloidal membranes

机译:非两亲性胶体膜的熵驱动自组装

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摘要

We demonstrate that homogeneous monodisperse rods in the presence of attractive interactions assemble into equilibrium 2D fluid-like membranes composed of a one-rod length thick monolayer of aligned rods. Unique features of our system allow us to simultaneously investigate properties of these membranes at both continuum and molecular lengthscales. Analysis of thermal fluctuations at continuum lengthscales yields the membranes’ lateral compressibility and bending rigidity and demonstrates that the properties of colloidal membranes are comparable to those of traditional lipid bilayers. Fluctuations at molecular lengthscales, in which single rods protrude from the membrane surface, are directly measured by comparing the positions of individual fluorescently labeled rods within a membrane to that of the membrane’s continuum conformation. As two membranes approach each other in suspension, protrusion fluctuations are suppressed leading to effective repulsive interactions. Motivated by these observations, we propose an entropic mechanism that explains the stability of colloidal membranes and offers a general design principle for the self-assembly of 2D nanostructured materials from rod-like molecules.
机译:我们证明在存在有吸引力的相互作用的情况下均质的单分散棒组装成平衡的二维流体状膜,该膜由一根杆长的单层对齐棒构成。我们系统的独特功能使我们能够同时在连续谱和分子长度尺度上研究这些膜的特性。对连续长度尺度的热波动进行分析,可以得出膜的侧向可压缩性和弯曲刚度,并证明胶体膜的性能可与传统脂质双层膜相媲美。通过将单个荧光标记的棒在膜中的位置与膜的连续体构象的位置进行比较,可以直接测量分子长度尺度上的波动,其中单个棒从膜表面突出。当两个膜在悬浮液中彼此接近时,突出的波动被抑制,从而导致有效的排斥相互作用。基于这些观察结果,我们提出了一种熵机制,该熵机制解释了胶体膜的稳定性,并提供了从棒状分子自组装二维纳米结构材料的一般设计原理。

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