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表面附近液-液界面处活性粒子的引导

Guidance of active particles at liquid-liquid interfaces near surfaces.

作者信息

Palacios Lucas S, Katuri Jaideep, Pagonabarraga Ignacio, Sánchez Samuel

机构信息

Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology (BIST), Baldiri Reixac 10-12, 08028 Barcelona, Spain.

Departament de Física de la Matèria Condensada, Universitat de Barcelona, 08028 Barcelona, Spain.

出版信息

Soft Matter. 2019 Aug 28;15(32):6581-6588. doi: 10.1039/c9sm01016e. Epub 2019 Jul 31.

Abstract

Artificial microswimmers have the potential for applications in many fields, ranging from targeted cargo delivery and mobile sensing to environmental remediation. In many of these applications, the artificial swimmers will operate in complex media necessarily involving liquid-liquid interfaces. Here, we experimentally study the motion of chemically powered phoretic active colloids close to liquid-liquid interfaces while swimming next to a solid substrate. In a system involving this complex geometry, we find that the active particles have an alignment interaction with both the neighbouring solid and liquid interfaces, allowing for a robust guiding mechanism along the liquid interface. We compare with minimal active Brownian simulations to show that these phoretically active particles stay along the interfaces for much longer times and lengths than expected for standard active Brownian particles. We also track the propulsion speeds of these particles and find a reduced speed close to the liquid-liquid interface. We report an interesting non-linear dependence of this reduction on the particle's bulk speed.

摘要

人工微游动器在许多领域都有应用潜力,从靶向货物运输、移动传感到环境修复。在许多此类应用中,人工游动器将在必然涉及液 - 液界面的复杂介质中运行。在此,我们通过实验研究了化学驱动的电泳活性胶体在靠近液 - 液界面且紧邻固体基质游动时的运动。在一个涉及这种复杂几何结构的系统中,我们发现活性粒子与相邻的固体和液体界面都存在排列相互作用,从而形成了一种沿液体界面的强大导向机制。我们与最小活性布朗模拟进行比较,结果表明,与标准活性布朗粒子相比,这些电泳活性粒子在界面上停留的时间和长度要长得多。我们还追踪了这些粒子的推进速度,发现靠近液 - 液界面时速度会降低。我们报告了这种速度降低对粒子体相速度的有趣非线性依赖关系。

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