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Jie Lin
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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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Recent experiments and simulations have revealed glassy features in the cytoplasm, living tissues as well as dense assemblies of self propelled colloids. This leads to a fundamental question: how do these non-equilibrium (active) amorphous materials differ from conventional passive glasses, created either by lowering temperature or by increasing density? To address this we investigate the aging behaviour after a quench to an almost arrested state of a model active glass former, a Kob-Andersen glass in two dimensions. Each constituent particle is driven by a constant propulsion force whose direction diffuses over time. Using extensive molecular dynamics simulations we reveal rich aging behaviour of this dense active matter system: short persistence times of the active forcing lead to effective thermal aging; in the opposite limit we find a two-step aging process with active athermal aging at short times followed by activity-driven aging at late times. We develop a dedicated simulation method that gives access to this long-time scaling regime for highly persistent active forces.
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 $d>2$.
We investigate the swim pressure exerted by non-chiral and chiral active particles on convex or concave circular boundaries. Active particles are modeled as non-interacting and non-aligning self-propelled Brownian particles. The convex and concave circular boundaries are used as models representing a fixed inclusion immersed in an active bath and a cavity (or container) enclosing the active particles, respectively. We first present a detailed analysis of the role of convex versus concave boundary curvature and of the chirality of active particles on their spatial distribution, chirality-induced currents, and the swim pressure they exert on the bounding surfaces. The results will then be used to predict the mechanical equilibria of suspended fluid enclosures (generically referred to as droplets) in a bulk with active particles being present either inside the bulk fluid or within the suspended droplets. We show that, while droplets containing active particles and suspended in a normal bulk behave in accordance with standard capillary paradigms, those containing a normal fluid exhibit anomalous behaviors when suspended in an active bulk. In the latter case, the excess swim pressure results in non-monotonic dependence of the inside droplet pressure on the droplet radius. As a result, we find a regime of anomalous capillarity for a single droplet, where the inside droplet pressure increases upon increasing the droplet size. In the case of two interconnected droplets, we show that mechanical equilibrium can occur also when they have different sizes. We further identify a regime of anomalous ripening, where two unequal-sized droplets can reach a final state of equal sizes upon interconnection, in stark contrast with the standard Ostwald ripening phenomenon, implying shrinkage of the smaller droplet in favor of the larger one.
This paper derives and discusses the configuration-space Langevin equation describing a physically aging R-simple system and the corresponding Smoluchowski equation. Externally controlled thermodynamic variables like temperature, density, pressure enter the description via the single parameter ${T}_{rm s}/T$ in which $T$ is the bath temperature and ${T}_{rm s}$ is the systemic temperature defined at any time $t$ as the thermodynamic equilibrium temperature of the state point with density $rho(t)$ and potential energy $U(t)$. In equilibrium ${T}_{rm s}cong T$ with fluctuations that vanish in the thermodynamic limit. In contrast to Tools fictive temperature and other effective temperatures in glass science, the systemic temperature is defined for any configuration with a well-defined density, even if it is not in any sense close to equilibrium. Density and systemic temperature define an aging phase diagram in which the aging system traces out a curve. Predictions are discussed for aging following various density-temperature and pressure-temperature jumps from one equilibrium state to another, as well as for a few other scenarios. The proposed theory implies that R-simple glass-forming liquids are characterized by a dynamic Prigogine-Defay ratio of unity.
The two-body (pair) contribution to the entropy of two-dimensional Yukawa systems is calculated and analyzed. It is demonstrated that in the vicinity of the fluid-solid (freezing) phase transition the pair entropy exhibits an abrupt jump in a narrow temperature range and this can be used to identify the freezing point. Relations to the full excess entropy and some existing freezing indicators are briefly discussed.
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