No Arabic abstract
Active fluids are intrinsically out-of-equilibrium systems due to the internal energy injection of the active constituents. We show here that a transition from a motion-less isotropic state towards a flowing polar one can be possibly driven by the sole active injection through the action of polar-hydrodynamic interactions in absence of an ad hoc free-energy which favors the development of an ordered phase. In particular, we propose an analytical argument and we perform lattice Boltzmann simulations where the appearance of large temporal fluctuations in the polar fraction of the system is observed at the transition point. Moreover, we make use of a scale-to-scale analysis to unveil the energy transfer mechanism, proving that elastic absorption plays a relevant role in the overall dynamics of the system, contrary to what reported in previous works on the usual active gel theory where this term could be factually neglected.
Despite their fundamentally non-equilibrium nature, the individual and collective behavior of active systems with polar propulsion and isotropic interactions (polar-isotropic active systems) are remarkably well captured by equilibrium mapping techniques. Here we examine two signatures of equilibrium systems -- the existence of a local free energy function and the independence of the coarse- grained behavior on the details of the microscopic dynamics -- in polar-isotropic active particles confined by hard walls of arbitrary geometry at the one-particle level. We find that boundaries that possess concave regions make the density profile strongly dynamics-dependent and give it a nonlocal dependence on the geometry of the confining box. This in turn constrains the scope of equilibrium mapping techniques in polar-isotropic active systems.
Starting from a microscopic definition of an alignment vector proportional to the polarization, we discuss the hydrodynamics of polar liquid crystals with local $C_{infty v}$-symmetry. The free energy for polar liquid crystals differs from that of nematic liquid crystals ($D_{infty h}$) in that it contains terms violating the ${bf{n}}to -{bf{n}}$ symmetry. First we show that these $mathcal{Z}_2$-odd terms induce a general splay instability of a uniform polarized state in a range of parameters. Next we use the general Poisson-bracket formalism to derive the hydrodynamic equations of the system in the polarized state. The structure of the linear hydrodynamic modes confirms the existence of the splay instability.
Blue phase liquid crystals are not usually considered to exhibit a flexoelectrooptic effect, due to the polar nature of flexoelectric switching and the cubic or amorphous structure of blue phases. Here, we derive the form of the flexoelectric contribution to the Kerr constant of blue phases, and experimentally demonstrate and measure the separate contributions to the Kerr constant arising from flexoelectric and dielectric effects. Hence, a non-polar flexoelectrooptic effect is demonstrated in blue phase liquid crystals, which will have consequences for the engineering of novel blue-phase electrooptic technology.
Turbulence in driven stratified active matter is considered. The relevant parameters characterizing the problem are the Reynolds number Re and an active matter Richardson-like number,R. In the mixing limit,Re>>1, R<<1, we show that the standard Kolmogorov energy spectrum 5/3 law is realized. On the other hand, in the stratified limit, Re>>1,R>>1, there is a new turbulence universality class with a 7/5 law. The crossover from one regime to the other is discussed in detail. Experimental predictions and probes are also discussed.
We study numerically the rheological properties of a slab of active gel close o the isotropic-nematic transition. The flow behavior shows strong dependence on sample size, boundary conditions, and on the bulk constitutive curve, which, on entering the nematic phase, acquires an activity-induced discontinuity at the origin. The precursor of this within the metastable isotropic phase for contractile systems ({em e.g.,} actomyosin gels) gives a viscosity divergence; its counterpart for extensile ({em e.g.,} {em B. subtilis}) suspensions admits instead a shear-banded flow with zero apparent viscosity.