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Register a new userCriticality in polar fluids
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A model of polar fluid is studied theoretically. The interaction potential, in addition to dipole-dipole term, possesses a dispersion contribution of the van der Waals-London form. It is found that when the dispersion force is comparable to dipole-dipole interaction, the fluid separates into coexisting liquid and gas phases. The calculated critical parameters are in excellent agreement with Monte Carlo simulations. When the strength of dispersion attraction is bellow critical, no phase separation is found.
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We study universal behavior in the moving phase of a generic system of motile particles with alignment interactions in the incompressible limit for spatial dimensions $d>2$. Using a dynamical renormalization group analysis, we obtain the exact dynamic, roughness, and anisotropy exponents that describe the scaling behavior of such incompressible systems. This is the first time a compelling argument has been given for the exact values of the anomalous scaling exponents of a flock moving through an isotropic medium in $d>2$.
Meso-scale turbulence was originally observed experimentally in various suspensions of swimming bacteria, as well as in the collective motion of active colloids. The corresponding large-scale dynamical patterns were reproduced in a simple model of a polar fluid, assuming a constant density of active particles. Recent, more detailed experimental studies revealed additional interesting aspects, such as anomalous velocity statistics and clustering phenomena. Those phenomena cannot be explained by currently available models for active polar fluids. Herein, we extend the continuum model suggested by Dunkel et al. to include density variations and a feedback between the local density and self-propulsion speed of the active particles. If the velocity decreases strong enough with the density, a linear stability analysis of the resulting model shows that, in addition to the short-wavelength instability of the original model, a long-wavelength instability occurs. This is typically observed for high densities of polar active particles and is analogous to the well-known phenomenon of motility-induced phase separation (MIPS) in scalar active matter. We determine a simple phase diagram indicating the linear instabilities and perform systematic numerical simulations for the various regions in the corresponding parameter space. The interplay between the well understood short-range instability and the long-range instability leads to interesting dynamics and novel phenomena concerning nucleation and coarsening processes. Our simulation results display a rich variety of novel patterns, including phase separation into domains with dynamically changing irregularly shaped boundaries. Anomalous velocity statistics are observed in all phases where the system segregates into regions of high and low densities. This offers a simple explanation for their occurrence in recent experiments with bacterial suspensions.
Spontaneous emergence of correlated states such as flocks and vortices are prime examples of remarkable collective dynamics and self-organization observed in active matter. The formation of globally correlated polar states in geometrically confined systems proceeds through the emergence of a macroscopic steadily rotating vortex that spontaneously selects a clockwise or counterclockwise global chiral state. Here, we reveal that a global vortex formed by colloidal rollers exhibits state memory. The information remains stored even when the energy injection is ceased and the activity is terminated. We show that a subsequent formation of the collective states upon re-energizing the system is not random. We combine experiments and simulations to elucidate how a combination of hydrodynamic and electrostatic interactions leads to hidden asymmetries in the local particle positional order encoding the chiral state of the system. The stored information can be accessed and exploited to systematically command subsequent polar states of active liquid through temporal control of the activity. With the chirality of the emergent collective states controlled on-demand, active liquids offer new possibilities for flow manipulation, transport, and mixing at the microscale.
Three one-body profiles that correspond to local fluctuations in energy, in entropy, and in particle number are used to describe the equilibrium properties of inhomogeneous classical many-body systems. Local fluctuations are obtained from thermodynamic differentiation of the density profile or equivalently from average microscopic covariances. The fluctuation profiles follow from functional generators and they satisfy Ornstein-Zernike relations. Computer simulations reveal markedly different fluctuations in confined fluids with Lennard-Jones, hard sphere, and Gaussian core interactions.
Many experiments show that protein condensates formed by liquid-liquid phase separation exhibit aging rheological properties. Quantitatively, recent experiments by Jawerth et al. (Science 370, 1317, 2020) show that protein condensates behave as aging Maxwell fluids with an increasing relaxation time as the condensates age. Despite the universality of this aging phenomenon, a theoretical understanding of this aging behavior is lacking. In this work, we propose a mesoscopic model of protein condensates in which a phase transition from aging phase to non-aging phase occurs as the control parameter changes, such as temperature. The model predicts that protein condensates behave as viscoelastic Maxwell fluids at all ages, with the macroscopic viscosity increasing over time. The model also predicts that protein condensates are non-Newtonian fluids under a constant shear rate with the shear stress increasing over time. Our model successfully explains multiple existing experimental observations and also makes general predictions that are experimentally testable.
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