Soft ULC Microgels at the Interface Interact and Flow as Hertzian‐Like Colloids
Advanced Materials Interfaces, vol. 12
Abstract
Abstract Soft pair potentials predict a reentrant liquid phase for high concentrations, a behavior not observed experimentally. Here, very soft microgels confined at an oil‐water interface are used as a model system of particles interacting via a soft potential in 2D. Interfacial rheology measurements demonstrate the existence of different flow regimes that depend on the compression of the monolayer. Such a compression also leads to a non‐monotonic variation of the elastic moduli and of the yield stress of the monolayer. These results, together with the equilibrium phase behavior of the monolayer, are reproduced in molecular dynamics simulations of a 2D system of particles interacting with a Hertzian‐like potential. Remarkably, due to the non‐monotonic variation of the elastic moduli, we observe isoelastic points where the monolayer shows the same stiffness at very different concentrations. These points are the experimental manifestation of the predicted reentrant liquid phase.
Authors 6
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Affiliation as printed
Department of Condensed Matter Physics University of Barcelona Barcelona 08028 Spain
Institute of Complex Systems (UBICS) University of Barcelona Barcelona 08028 Spain
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Affiliation as printed
Institute of Physical Chemistry RWTH Aachen University Landoltweg 2 52074 Aachen Germany
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Affiliation as printed
Institute of Physical Chemistry RWTH Aachen University Landoltweg 2 52074 Aachen Germany
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Affiliation as printed
Institute of Physical Chemistry RWTH Aachen University Landoltweg 2 52074 Aachen Germany
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Emanuela Zaccarelli corresponding
Institute for Complex Systems · National Research Council · Sapienza University of Rome
Affiliation as printed
Department of Physics Sapienza University of Rome Piazzale Aldo Moro 2 Rome 00185 Italy
Italian National Research Council ‐ Institute for Complex Systems (CNR‐ISC) Sapienza University of Rome Piazzale Aldo Moro 5 Rome 00185 Italy
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Andrea Scotti corresponding
Affiliation as printed
Division of Physical Chemistry Lund University Lund SE‐22100 Sweden
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