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H. H. Wensink

Publications and source records attributed to H. H. Wensink.

34 records · Page 2Linked to original sources

Controlling active self-assembly through broken particle symmetries

Many structural properties of conventional passive materials are known to arise from the symmetries of their microscopic constituents. By contrast, it is largely unclear how the interplay between cell shape and self-propulsion controls the meso- and macroscale behavior of active matter. Here, we analyze large-scale simulations of homo- and heterogeneous self-propelled particle systems to identify generic effects of broken particle symmetry on collective motion. We find that even small violations of fore-aft symmetry lead to fundamentally different collective behaviors, which may facilitate demixing of differently shaped species as well as the spontaneous formation of stable micro-rotors. These results suggest that variation of particle shape yields robust physical mechanisms to control self-assembly of active matter, with possibly profound implications for biology and materials design.

cond-mat.soft↗

Emergent states in dense systems of active rods: from swarming to turbulence

Dense suspensions of self-propelled rod-like particles exhibit a fascinating variety of non-equilibrium phenomena. By means of computer simulations of a minimal model for rigid self-propelled colloidal rods with variable shape we explore the generic diagram of emerging states over a large range of rod densities and aspect ratios. The dynamics is studied using a simple numerical scheme for the overdamped noiseless frictional dynamics of a many-body system in which steric forces are dominant over hydrodynamic ones. The different emergent states are identified by various characteristic correlation functions and suitable order parameter fields. At low density and aspect ratio, a disordered phase with no coherent motion precedes a highly-cooperative swarming state at large aspect ratio. Conversely, at high densities weakly anisometric particles show a distinct jamming transition whereas slender particles form dynamic laning patterns. In between there is a large window corresponding to strongly vortical, turbulent flow. The different dynamical states should be verifiable in systems of swimming bacteria and artificial rod-like micro-swimmers.

cond-mat.soft↗

How to capture active particles

For many applications, it is important to catch collections of autonomously navigating microbes and man-made microswimmers in a controlled way. Here we propose an efficient trap to collectively capture self-propelled colloidal rods. By means of computer simulation in two dimensions, we show that a static chevron-shaped wall represents an optimal boundary for a trapping device. Its catching efficiency can be tuned by varying the opening angle of the trap. For increasing angles, there is a sequence of three emergent states corresponding to partial, complete, and no trapping. A trapping `phase diagram' maps out the trap conditions under which the capture of self-propelled particles at a given density is rendered optimal.

cond-mat.soft↗

Cholesteric order in systems of helical Yukawa rods

We consider the interaction potential between two chiral rod-like colloids which consist of a thin cylindrical backbone decorated with a helical charge distribution on the cylinder surface. For sufficiently slender coiled rods a simple scaling expression is derived which links the chiral `twisting' potential to the intrinsic properties of the particles such as the coil pitch, charge density and electrostatic screening parameter. To predict the behavior of the macroscopic cholesteric pitch we invoke a simple second-virial theory generalized for weakly twisted director fields. While the handedness of the cholesteric phase for weakly coiled rods is always commensurate with that of the internal coil, more strongly coiled rods display cholesteric order with opposite handedness. The correlation between the symmetry of the microscopic helix and the macroscopic cholesteric director field is quantified in detail. Mixing helices with sufficiently disparate lengths and coil pitches gives rise to a demixing of the uniform cholesteric phase into two fractions with a different macroscopic pitch. Our findings are consistent with experimental results and could be helpful in interpreting experimental observations in systems of cellulose and chitin microfibers, DNA and {\em fd} virus rods.

cond-mat.soft↗

Phase diagram of hard colloidal platelets: a theoretical account

We construct the complete liquid crystal phase diagram of hard plate-like cylinders for variable aspect ratio using Onsager's second virial theory with the Parsons-Lee decoupling approximation to account for higher-body interactions in the isotropic and nematic fluid phases. The stability of the solid (columnar) state at high packing fraction is included by invoking a simple equation of state based on a Lennard-Jones-Devonshire (LJD) cell model which has proven to be quantitatively reliable over a large range of packing fractions. By employing an asymptotic analysis based on the Gaussian approximation we are able to show that the nematic-columnar transition is universal and independent of particle shape. The predicted phase diagram is in qualitative agreement with simulation results.

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Supersaturated dispersions of rod-like viruses with added attraction

The kinetics of isotropic-nematic (I-N) and nematic-isotropic (N-I) phase transitions in dispersions of rod-like {\it fd}-viruses are studied. Concentration quenches were applied using pressure jumps in combination with polarization microscopy, birefringence and turbidity measurements. The full biphasic region could be accessed, resulting in the construction of a first experimental analogue of the bifurcation diagram. The N-I spinodal points for dispersions of rods with varying concentrations of depletion agents (dextran) were obtained from orientation quenches, using cessation of shear flow in combination with small angle light scattering. We found that the location of the N-I spinodal point is independent of the attraction, which was confirmed by theoretical calculations. Surprisingly, the experiments showed that also the absolute induction time, the critical nucleus and the growth rate are insensitive of the attraction, when the concentration is scaled to the distance to the phase boundaries.

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Generalized van der Waals theory for the twist elastic modulus and helical pitch of cholesterics

We present a generalized van der Waals theory for a lyotropic cholesteric system of chiral spherocylinders based on the classical Onsager theory for hard anisometric bodies. The rods consist of a hard spherocylindrical backbone surrounded with a square-well potential to account for attractive (or soft repulsive) interactions. Long-ranged chiral interactions are described by means of a simple pseudo-scalar potential which is appropriate for weak chiral forces of a predominant electrostatic origin. Based on the formalism proposed by Straley [Phys. Rev. A {\bf 14}, 1835 (1976)] we derive explicit algebraic expressions for the twist elastic modulus and the cholesteric pitch for rods as a function of density and temperature. The pitch varies non-monotonically with density, with a sharp decrease at low packing fractions and a marked increase at higher packing fractions. A similar trend is found for the temperature dependence. The unwinding of the helical pitch at high densities (or low temperatures) originates from a marked increase in the local nematic order and a steep increase of the twist elastic resistance associated with near-parallel local rod configurations. This contrasts with the commonly held view that the increase in pitch with decreasing temperature as often observed in cholesterics is due to layer formation resulting from pre-smectic fluctuations. The increase in pitch with increasing temperature is consistent with an entropic unwinding as the chiral interaction becomes less and less significant than the thermal energy. The variation of the pitch with density, temperature and contour length is in qualitative agreement with recent experimental results on colloidal {\em fd} rods.

cond-mat.soft↗

Aggregation of self-propelled colloidal rods near confining walls

Non-equilibrium collective behavior of self-propelled colloidal rods in a confining channel is studied using Brownian dynamics simulations and dynamical density functional theory. We observe an aggregation process in which rods self-organize into transiently jammed clusters at the channel walls. In the early stage of the process, fast-growing hedgehog-like clusters are formed which are largely immobile. At later stages, most of these clusters dissolve and mobilize into nematized aggregates sliding past the walls.

cond-mat.soft↗

Long-time self-diffusion of Brownian Gaussian-core particles

Using extensive Brownian dynamics computer simulations, the long-time self-diffusion coefficient is calculated for Gaussian-core particles as a function of the number density. Both spherical and rod-like particles interacting via Gaussian segments ar$ For increasing concentration we find that the translational self-diffusion behaves non-monotonically reflecting the structural reentrance effect in the equilibrium phase diagram. Both in the limits of zero and infinite concentration, it approaches its short-time value. The microscopic Medina-Noyola theory qualitatively accounts for the translational long-time diffusion. The long-time orientational diffusion coefficient for Gaussian rods, on the other hand, remains very close to its short-time counterpart for any density. Some implications of the weak translation-rotation coupling for ultrasoft rods are discussed.

cond-mat.soft↗

First-order phase transitions in two-dimensional off-lattice liquid crystals

We consider an off-lattice liquid crystal pair potential in strictly two dimensions. The potential is purely repulsive and short-ranged. Nevertheless, by means of a single parameter in the potential, the system is shown to undergo a first-order phase transition. The transition is studied using mean-field density functional theory, and shown to be of the isotropic-to-nematic kind. In addition, the theory predicts a large density gap between the two coexisting phases. The first-order nature of the transition is confirmed using computer simulation and finite-size scaling. Also presented is an analysis of the interface between the coexisting domains, including estimates of the line tension, as well as an investigation of anchoring effects.

cond-mat.soft↗

Columnar versus smectic order in systems of charged colloidal rods

We study the stability of inhomogeneous liquid crystalline states in systems of monodisperse, stiff, charged rods. By means of a bifurcation analysis applied to the Onsager free energy for charged rods in strongly nematic states, we investigate nematic-smectic and nematic-columnar instabilities as a function of the Debye screening length. While the nematic-smectic transition clearly pre-emts the nematic-columnar one in the regime of strong screening a marked stability of hexagonal columnar order is observed at larger screening lengths. The theoretical results are substantiated by Brownian dynamics computer simulation results based on the Yukawa-site model. Our findings connect to experiments on tobacco mosaic virus rods in particular but might be relevant for soft rod-like mesogens in strong external directional fields in general.

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Rhythmic cluster generation in strongly driven colloidal dispersions

We study the response of a nematic colloidal dispersion of rods to a driven probe particle which is dragged with high speed through the dispersion perpendicular to the nematic director. In front of the dragged particle, clusters of rods are generated which rhythmically grow and dissolve by rotational motion. We find evidence for a mesoscopic cluster-cluster correlation length, {\em independent} of the imposed drag speed. Our results are based on non-equilibrium Brownian dynamics computer simulations and in line with a dynamical scaling theory.

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Coexistence diameter in two-dimensional colloid-polymer mixtures

We demonstrate that the law of the rectilinear coexistence diameter in two-dimensional (2D) mixtures of non-spherical colloids and non-adsorbing polymers is violated. Upon approach of the critical point, the diameter shows logarithmic singular behavior governed by a term t ln(t), with t the relative distance from the critical point. No sign of a term t^2b could be detected, with b the critical exponent of the order parameter, indicating a very weak or absent Yang-Yang anomaly. Our analysis thus reveals that non-spherical particle shape alone is not sufficient for the formation of a pronounced Yang-Yang anomaly in the critical behavior of fluids.

cond-mat.stat-mech↗

Nematic order of model goethite nanorods in a magnetic field

We explore the nematic order of model goethite nanorods in an external magnetic field within Onsager-Parsons density functional theory. The goethite rods are represented by monodisperse, charged spherocylinders with a permanent magnetic moment along the rod main axis, forcing the particles to align parallel to the magnetic field at low field strength. The intrinsic diamagnetic susceptibility anisometry of the rods is negative which leads to a preferred perpendicular orientation at higher field strength. It is shown that these counteracting effects may give rise to intricate phase behavior, including a pronounced stability of biaxial nematic order and the presence of reentrant phase transitions and demixing phenomena. The effect of the applied field on the nematic-to-smectic transition will also be addressed.

cond-mat.soft↗

On the equation of state of a dense columnar liquid crystal

An accurate description of a columnar liquid crystal of hard disks at high packing fractions is presented using an improved free-volume theory. It is shown that the orientational entropy of the disks in the one-dimensional fluid direction leads to a different high-density scaling pressure compared to the prediction from traditional cell theory. Excellent quantitative agreement is found with recent Monte-Carlo simulation results for various thermodynamic and structural properties of the columnar state.

cond-mat.stat-mech↗

Isotropic-nematic phase behavior of length polydisperse hard rods

The isotropic-nematic phase behavior of length polydisperse hard rods with arbitrary length distributions is calculated. Within a numerical treatment of the polydisperse Onsager model using the Gaussian trial function Ansatz we determine the onset of isotropic-nematic phase separation, coming from a dilute isotropic phase and a dense nematic phase. We focus on parent systems whose lengths can be described by either a Schulz or a `fat-tailed' log-normal distribution with appropriate lower and upper cutoff lengths. In both cases, very strong fractionation effects are observed for parent polydispersities larger than roughly 50 %. In these regimes, the isotropic and nematic phases are completely dominated by respectively the shortest and the longest rods in the system. Moreover, for the log-normal case, we predict triphasic isotropic-nematic-nematic equilibria to occur above a certain threshold polydispersity. By investigating the properties of the coexisting phases across the coexistence region for a particular set of cutoff lengths we explicitly show that the region of stable triphasic equilibria does not extend up to very large parent polydispersities but closes off at a consolute point located not far above the threshold polydispersity. The experimental relevance of the phenomenon is discussed.

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