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      How to steer active colloids up a vertical wall

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          Abstract

          An important challenge in active matter lies in harnessing useful global work from entities that produce work locally, e.g., via self-propulsion. We investigate here the active matter version of a classical capillary rise effect, by considering a non-phase separated sediment of self-propelled Janus colloids in contact with a vertical wall. We provide experimental evidence of an unexpected and dynamic adsorption layer at the wall. Additionally, we develop a complementary numerical model that recapitulates the experimental observations. We show that an adhesive and aligning wall enhances the pre-existing polarity heterogeneity within the bulk, enabling polar active particles to climb up a wall against gravity, effectively powering a global flux. Such steady-state flux has no equivalent in a passive wetting layer.

          Abstract

          It has been demonstrated theoretically earlier that a dense phase made of repulsive active particles, in phase-separating regime, exhibit wetting-like behaviors: wall-meniscus or capillary rise in channels. Here authors experimentally investigate a non-phase separating assembly of active colloids under gravity and show that a wetting-like phenomenology persists against a vertical wall, and they evidence a counter-gravity wall climbing.

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          Most cited references41

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          Catalytic nanomotors: autonomous movement of striped nanorods.

          Rod-shaped particles, 370 nm in diameter and consisting of 1 microm long Pt and Au segments, move autonomously in aqueous hydrogen peroxide solutions by catalyzing the formation of oxygen at the Pt end. In 2-3% hydrogen peroxide solution, these rods move predominantly along their axis in the direction of the Pt end at speeds of up to 10 body lengths per second. The dimensions of the rods and their speeds are similar to those of multiflagellar bacteria. The force along the rod axis, which is on the order of 10(-14) N, is generated by the oxygen concentration gradient, which in turn produces an interfacial tension force that balances the drag force at steady state. By solving the convection-diffusion equation in the frame of the moving rod, it was found that the interfacial tension force scales approximately as SR(2)gamma/muDL, where S is the area-normalized oxygen evolution rate, gamma is the liquid-vapor interfacial tension, R is the rod radius, mu is the viscosity, D is the diffusion coefficient of oxygen, and L is the length of the rod. Experiments in ethanol-water solutions confirmed that the velocity depends linearly with the product Sgamma, and scaling experiments showed a strong dependence of the velocity on R and L. The direction of motion implies that the gold surface is hydrophobic under the conditions of the experiment. Tapping-mode AFM images of rods in air-saturated water show soft features that are not apparent in images acquired in air. These features are postulated to be nanobubbles, which if present in hydrogen peroxide solutions, would account for the observed direction of motion.
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            Motility-Induced Phase Separation

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              Hydrodynamic attraction of swimming microorganisms by surfaces.

              Cells swimming in confined environments are attracted by surfaces. We measure the steady-state distribution of smooth-swimming bacteria (Escherichia coli) between two glass plates. In agreement with earlier studies, we find a strong increase of the cell concentration at the boundaries. We demonstrate theoretically that hydrodynamic interactions of the swimming cells with solid surfaces lead to their reorientation in the direction parallel to the surfaces, as well as their attraction by the closest wall. A model is derived for the steady-state distribution of swimming cells, which compares favorably with our measurements. We exploit our data to estimate the flagellar propulsive force in swimming E. coli.
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                Author and article information

                Contributors
                heiko.rieger@uni-saarland.de
                cecile.cottin-bizonne@univ-lyon1.fr
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                24 February 2024
                24 February 2024
                2024
                : 15
                : 1710
                Affiliations
                [1 ]GRID grid.436142.6, ISNI 0000 0004 0384 4911, Université de Lyon, Université Claude Bernard Lyon 1, CNRS, Institut Lumière Matière, ; Villeurbanne, France
                [2 ]Department of Theoretical Physics and Center for Biophysics, Saarland University, ( https://ror.org/01jdpyv68) Saarbrücken, Germany
                [3 ]Leibniz Institute for New Materials INM, ( https://ror.org/00g656d67) Saarbrücken, Germany
                Author information
                http://orcid.org/0000-0002-2793-7229
                http://orcid.org/0000-0002-4754-8933
                http://orcid.org/0000-0003-0205-3678
                http://orcid.org/0000-0001-5807-9215
                Article
                45872
                10.1038/s41467-024-45872-1
                10894264
                38402227
                59a95e27-865d-4085-a5de-d69e19b60bcb
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 28 June 2023
                : 5 February 2024
                Categories
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                © Springer Nature Limited 2024

                Uncategorized
                physics,colloids
                Uncategorized
                physics, colloids

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