Celso CarrascoUC San Diego, Quentin MartinetIST Austria, Zaiyi ShenLOMA, Juho S. LintuvuoriLOMA, Jérémie PalacciIST Austria, Antoine AubretLOMA
{"title":"Quantitative measurements of non-equilibrium interactions of catalytic microswimmers with dual colloidal tracers","authors":"Celso CarrascoUC San Diego, Quentin MartinetIST Austria, Zaiyi ShenLOMA, Juho S. LintuvuoriLOMA, Jérémie PalacciIST Austria, Antoine AubretLOMA","doi":"arxiv-2409.01024","DOIUrl":null,"url":null,"abstract":"Catalytic microswimmers convert the chemical energy of a fuel into motion,\nsustaining spatial chemical gradients and fluid flows that drive their\npropulsion. This leads to unconventional individual behavior and the emergence\nof collective dynamics, absent in equilibrium. The characterization of the\nnonequilibrium interactions driven by those concentration gradients and flows\naround microswimmers is challenging owing to the importance of fluctuations at\nthe microscale. Previous experiments have focused on large Janus microspheres\nattached to a surface, and did not investigate non-equilibrium interactions for\nfreely moving microswimmers of various shapes. Here we show a massive\ndependence of the non-equilibrium interactions on the shape of small catalytic\nmicroswimmers. We perform tracking experiments at high troughput to map\nnon-equilibrium interactions between swimmers and colloidal tracers in 2D,\naccurate down to tracer velocity of 100nm/s. In addition, we devise a novel\nexperimental method combining two types of tracers with differing phoretic\nmobility to disentangle phoretic interactions in concentration gradients from\nhydrodynamic flows. We benchmark the method with experiments on a single\nchemically active site and on a catalytic microswimmer tethered to a surface.\nWe further investigate the activity-driven interactions of freely moving\ncatalytic dimers as microswimmers, for a wide range of aspect ratio between the\nactive and passive part. We confront our results with standard theoretical\nmodels of microswimmers near surfaces and show poor agreement, ruling out\nphoresis as the main interaction for catalytic swimmers. Our findings provide\nrobust quantitative measurements of the non-equilibrium interactions of\ncatalytic microswimmers of various geometry with their environment. The work\nnotably indicates the need for theoretical development, and lays the groundwork\nfor the quantitative description of collective behavior in suspensions of\nphoretically-driven colloidal suspensions.","PeriodicalId":501146,"journal":{"name":"arXiv - PHYS - Soft Condensed Matter","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - PHYS - Soft Condensed Matter","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.01024","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Catalytic microswimmers convert the chemical energy of a fuel into motion,
sustaining spatial chemical gradients and fluid flows that drive their
propulsion. This leads to unconventional individual behavior and the emergence
of collective dynamics, absent in equilibrium. The characterization of the
nonequilibrium interactions driven by those concentration gradients and flows
around microswimmers is challenging owing to the importance of fluctuations at
the microscale. Previous experiments have focused on large Janus microspheres
attached to a surface, and did not investigate non-equilibrium interactions for
freely moving microswimmers of various shapes. Here we show a massive
dependence of the non-equilibrium interactions on the shape of small catalytic
microswimmers. We perform tracking experiments at high troughput to map
non-equilibrium interactions between swimmers and colloidal tracers in 2D,
accurate down to tracer velocity of 100nm/s. In addition, we devise a novel
experimental method combining two types of tracers with differing phoretic
mobility to disentangle phoretic interactions in concentration gradients from
hydrodynamic flows. We benchmark the method with experiments on a single
chemically active site and on a catalytic microswimmer tethered to a surface.
We further investigate the activity-driven interactions of freely moving
catalytic dimers as microswimmers, for a wide range of aspect ratio between the
active and passive part. We confront our results with standard theoretical
models of microswimmers near surfaces and show poor agreement, ruling out
phoresis as the main interaction for catalytic swimmers. Our findings provide
robust quantitative measurements of the non-equilibrium interactions of
catalytic microswimmers of various geometry with their environment. The work
notably indicates the need for theoretical development, and lays the groundwork
for the quantitative description of collective behavior in suspensions of
phoretically-driven colloidal suspensions.