Mesoscopic fluxes in chemically driven phase-separated fluids originate from non-equilibrium interfacial statistics, and a FLEX-based hybrid theory predicts coexistence curves, flux localization, and droplet size scaling.
Critical transition between intensive and extensive active droplets
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abstract
Emulsions ripen with an average droplet size increasing in time. In chemically active emulsions, coarsening can be absent, leading to a non-equilibrium steady state with mono-disperse droplet sizes. By considering a minimal model for phase separation and chemical reactions maintained away from equilibrium, we show that there is a critical transition in the conserved quantity between two classes of chemically active droplets: intensive and extensive ones. Single intensive active droplets reach a stationary size mainly controlled by the reaction-diffusion length scales. Intensive droplets in an emulsion interact only weakly, and the stationary size of a single droplet approximately sets the size of each droplet. On the contrary, the size of a single extensive active droplet scales with the system size, similar to passive phases. In an emulsion of many extensive droplets, their sizes become stationary only due to interactions among them. We discuss how the critical transition between intensive and extensive active droplets affects shape instabilities, including the division of active droplets, paving the way for the observation of successive division events in chemically active emulsions
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cond-mat.soft 1years
2025 1verdicts
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Interfacial Effects Determine Nonequilibrium Phase Behaviors in Chemically Driven Fluids
Mesoscopic fluxes in chemically driven phase-separated fluids originate from non-equilibrium interfacial statistics, and a FLEX-based hybrid theory predicts coexistence curves, flux localization, and droplet size scaling.