Light-controlled assembly of active colloidal molecules

Thanks to a constant energy input, active matter can self-assemble into phases with complex architectures and functionalities such as living clusters that dynamically form, reshape, and break-up, which are forbidden in equilibrium materials by the entropy maximization (or free energy minimization) p...

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Veröffentlicht in:The Journal of chemical physics 2019-03, Vol.150 (9), p.094905-094905
Hauptverfasser: Schmidt, Falko, Liebchen, Benno, Löwen, Hartmut, Volpe, Giovanni
Format: Artikel
Sprache:eng
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Zusammenfassung:Thanks to a constant energy input, active matter can self-assemble into phases with complex architectures and functionalities such as living clusters that dynamically form, reshape, and break-up, which are forbidden in equilibrium materials by the entropy maximization (or free energy minimization) principle. The challenge to control this active self-assembly has evoked widespread efforts typically hinging on engineering of the properties of individual motile constituents. Here, we provide a different route, where activity occurs as an emergent phenomenon only when individual building blocks bind together in a way that we control by laser light. Using experiments and simulations of two species of immotile microspheres, we exemplify this route by creating active molecules featuring a complex array of behaviors, becoming migrators, spinners, and rotators. The possibility to control the dynamics of active self-assembly via light-controllable nonreciprocal interactions will inspire new approaches to understand living matter and to design active materials.
ISSN:0021-9606
1089-7690
DOI:10.1063/1.5079861