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活性胶体中的相互作用。

Interactions in active colloids.

作者信息

Liebchen Benno, Mukhopadhyay Aritra K

机构信息

Institute for Condensed Matter Physics, Technische Universität Darmstadt, 64289 Darmstadt, Germany.

出版信息

J Phys Condens Matter. 2021 Dec 9;34(8). doi: 10.1088/1361-648X/ac3a86.

DOI:10.1088/1361-648X/ac3a86
PMID:34788232
Abstract

The past two decades have seen a remarkable progress in the development of synthetic colloidal agents which are capable of creating directed motion in an unbiased environment at the microscale. These self-propelling particles are often praised for their enormous potential to self-organize into dynamic nonequilibrium structures such as living clusters, synchronized super-rotor structures or self-propelling molecules featuring a complexity which is rarely found outside of the living world. However, the precise mechanisms underlying the formation and dynamics of many of these structures are still barely understood, which is likely to hinge on the gaps in our understanding of how active colloids interact. In particular, besides showing comparatively short-ranged interactions which are well known from passive colloids (Van der Waals, electrostatic etc), active colloids show novel hydrodynamic interactions as well as phoretic and substrate-mediated 'osmotic' cross-interactions which hinge on the action of the phoretic field gradients which are induced by the colloids on other colloids in the system. The present article discusses the complexity and the intriguing properties of these interactions which in general are long-ranged, non-instantaneous, non-pairwise and non-reciprocal and which may serve as key ingredients for the design of future nonequilibrium colloidal materials. Besides providing a brief overview on the state of the art of our understanding of these interactions a key aim of this review is to emphasize open key questions and corresponding open challenges.

摘要

在过去二十年中,合成胶体剂的发展取得了显著进展,这些胶体剂能够在微观尺度的无偏环境中产生定向运动。这些自推进粒子因其巨大的潜力而备受赞誉,它们能够自组织成动态非平衡结构,如活性簇、同步超转子结构或自推进分子,其复杂性在生物界之外很少见。然而,许多这些结构的形成和动力学背后的确切机制仍然几乎不为人所知,这可能取决于我们对活性胶体如何相互作用的理解上的差距。特别是,除了表现出被动胶体中常见的相对短程相互作用(范德华力、静电力等)外,活性胶体还表现出新颖的流体动力学相互作用以及电泳和底物介导的“渗透”交叉相互作用,这些相互作用取决于胶体在系统中对其他胶体诱导的电泳场梯度的作用。本文讨论了这些相互作用的复杂性和有趣特性,这些相互作用通常是长程的、非瞬时的、非成对的和非互易的,并且可能作为未来非平衡胶体材料设计的关键要素。除了简要概述我们对这些相互作用的理解现状外,本综述的一个关键目标是强调未解决的关键问题和相应的开放挑战。

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