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Register a new userNematic and Polar order in Active Filament Solutions
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Added by
M. Cristina Marchetti
Publication date
2005
fields
Physics
and research's language is
English
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Using a microscopic model of interacting polar biofilaments and motor proteins, we characterize the phase diagram of both homogeneous and inhomogeneous states in terms of experimental parameters. The polarity of motor clusters is key in determining the organization of the filaments in homogeneous isotropic, polarized and nematic states, while motor-induced bundling yields spatially inhomogeneous structures.
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The nematic ordering in semiflexible polymers with contour length $L$ exceeding their persistence length $ell_p$ is described by a confinement of the polymers in a cylinder of radius $r_{eff}$ much larger than the radius $r_rho$, expected from the respective concentration of the solution. Large scale Molecular Dynamics simulations combined with Density Functional Theory are used to locate the Isotropic-Nematic ($I-N$)-transition and to validate this cylindrical confinement. Anomalous fluctuations, due to chain deflections from neighboring chains in the nematic phase are proposed. Considering deflections as collective excitations in the nematically ordered phase of semiflexible polymers elucidates the origins of shortcomings in the description of the $I-N$ transition by existing theories.
We introduce a lattice model for active nematic composed of self-propelled apolar particles,study its different ordering states in the density-temperature parameter space, and compare with the corresponding equilibrium model. The active particles interact with their neighbours within the framework of the Lebwohl-Lasher model, and move anisotropically along their orientation to an unoccupied nearest neighbour lattice site. An interplay of the activity, thermal fluctuations and density gives rise distinct states in the system. For a fixed temperature, the active nematic shows a disordered isotropic state, a locally ordered inhomogeneous mixed state, and bistability between the inhomogeneous mixed and a homogeneous globally ordered state in different density regime. In the low temperature regime, the isotropic to the inhomogeneous mixed state transition occurs with a jump in the order parameter at a density less than the corresponding equilibrium disorder-order transition density. Our analytical calculations justify the shift in the transition density and the jump in the order parameter. We construct the phase diagram of the active nematic in the density-temperature plane.
We introduce and study in two dimensions a new class of dry, aligning, active matter that exhibits a direct transition to orientational order, without the phase-separation phenomenology usually observed in this context. Characterized by self-propelled particles with velocity reversals and ferromagnetic alignment of polarities, systems in this class display quasi-long-range polar order with continuously-varying scaling exponents and yet a numerical study of the transition leads to conclude that it does not belong to the Berezinskii-Kosterlitz-Thouless universality class, but is best described as a standard critical point with algebraic divergence of correlations. We rationalize these findings by showing that the interplay between order and density changes the role of defects.
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.
Motility-induced phase separation is a purely non-equilibrium phenomenon in which self-propelled particles aggregate without any attractive interactions. One surprising feature of MIPS is the emergence of polar-nematic order at the interfacial region, whose underlying physics remains poorly understood. Here, I will show analytically and numerically that the many-body physics leading to the interfacial ordering behavior can be captured by an effective speed model. In this model, each particles speed depends on the systems density a short distance ahead of its direction of motion.
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