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Transient fluctuation-induced forces in driven electrolytes after an electric field quench

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Mahdisoltani,  Saeed
Department of Living Matter Physics, Max Planck Institute for Dynamics and Self-Organization, Max Planck Society;

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Golestanian,  Ramin       
Department of Living Matter Physics, Max Planck Institute for Dynamics and Self-Organization, Max Planck Society;

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Citation

Mahdisoltani, S., & Golestanian, R. (2021). Transient fluctuation-induced forces in driven electrolytes after an electric field quench. New Journal of Physics, 23: 073034. doi:10.1088/1367-2630/ac0f1a.


Cite as: https://hdl.handle.net/21.11116/0000-0008-D6C5-8
Abstract
Understanding how electrolyte solutions behave out of thermal equilibrium is a long-standing endeavour in many areas of chemistry and biology. Although mean-field theories are widely used to model the dynamics of electrolytes, it is also important to characterize the effects of fluctuations in these systems. In a previous work, we showed that the dynamics of the ions in a strong electrolyte that is driven by an external electric field can generate long-ranged correlations manifestly different from the equilibrium screened correlations; in the nonequilibrium steady state, these correlations give rise to a novel long-range fluctuation-induced force (FIF). Here, we extend these results by considering the dynamics of the strong electrolyte after it is quenched from thermal equilibrium upon the application of a constant electric field. We show that the asymptotic long-distance limit of both charge and density correlations is generally diffusive in time. These correlations give rise to long-ranged FIFs acting on the neutral confining plates with long-time regimes that are governed by power-law temporal decays toward the steady-state value of the force amplitude. These findings show that nonequilibrium uctuations have nontrivial implications on the dynamics of objects immersed in a driven electrolyte, and they could be useful for exploring new ways of controlling long-distance forces in charged solutions.