arXiv subjects

Hartmut Löwen

Publications and source records attributed to Hartmut Löwen.

At least 163 records · Page 9Linked to original sources

arXiv2019

Theory of active particle penetration through a planar elastic membrane

With the rapid advent of biomedical and biotechnological innovations, a deep understanding of the nature of interaction between nanomaterials and cell membranes, tissues, and organs, has become increasingly important. Active penetration of nanoparticles through cell membranes is a fascinating phenomenon that may have important implications in various biomedical and clinical applications. Using a fully analytical theory supplemented by particle-based computer simulations, the penetration process of an active particle through a planar two-dimensional elastic membrane is studied. The membrane is modeled as a self-assembled sheet of particles, uniformly arranged on a square lattice. A coarse-grained model is introduced to describe the mutual interactions between the membrane particles. The active penetrating particle is assumed to interact sterically with the membrane particles. State diagrams are presented to fully characterize the system behavior as functions of the relevant control parameters governing the transition between different dynamical states. Three distinct scenarios are identified. These compromise trapping of the active particle, penetration through the membrane with subsequent self-healing, in addition to penetration with permanent disruption of the membrane. The latter scenario is accompanied by a partial fragmentation of the membrane and creation of a hole of a size exceeding the interaction range of the membrane components. Our analytical theory is based on a combination of a perturbative expansion technique and a discrete-to-continuum formulation. Our approach might be helpful for the prediction of the transition threshold between the trapping and penetration in real-space experiments involving motile swimming bacteria or artificial active particles.

cond-mat.soft↗

arXiv2019

Frequency-dependent higher-order Stokes singularities near a planar elastic boundary: implications for the hydrodynamics of an active microswimmer near an elastic interface

The emerging field of self-driven active particles in fluid environments has recently created significant interest in the biophysics and bioengineering communities owing to their promising future biomedical and technological applications. These microswimmers move autonomously through aqueous media where under realistic situations they encounter a plethora of external stimuli and confining surfaces with peculiar elastic properties. Based on a far-field hydrodynamic model, we present an analytical theory to describe the physical interaction and hydrodynamic couplings between a self-propelled active microswimmer and an elastic interface that features resistance toward shear and bending. We model the active agent as a superposition of higher-order Stokes singularities and elucidate the associated translational and rotational velocities induced by the nearby elastic boundary. Our results show that the velocities can be decomposed in shear and bending related contributions which approach the velocities of active agents close to a no-slip rigid wall in the steady limit. The transient dynamics predict that contributions to the velocities of the microswimmer due to bending resistance are generally more pronounced than to shear resistance. Our results provide insight into the control and guidance of artificial and synthetic self-propelling active microswimmers near elastic confinements.

physics.flu-dyn↗

arXiv2019

Creeping motion of a solid particle inside a spherical elastic cavity. II. Asymmetric motion

An analytical method is proposed for computing the low-Reynolds-number hydrodynamic mobility function of a small colloidal particle asymmetrically moving inside a large spherical elastic cavity, the membrane of which is endowed with resistance toward shear and bending. In conjunction with the results obtained in the first part [Daddi-Moussa-Ider, Löwen, and Gekle, Eur. Phys. J. E 41, 104 (2018)], in which the axisymmetric motion normal to the surface of an elastic cavity is investigated, the general motion for an arbitrary force direction can be addressed. The elastohydrodynamic problem is formulated and solved using the classic method of images through expressing the hydrodynamic flow fields as a multipole expansion involving higher-order derivatives of the free-space Green's function. In the quasi-steady limit, we demonstrate that the particle self-mobility function of a particle moving tangent to the surface of the cavity is larger than that predicted inside a rigid stationary cavity of equal size. This difference is justified by the fact that a stationary rigid cavity introduces additional hindrance to the translational motion of the encapsulated particle, resulting in a reduction of its hydrodynamic mobility. Furthermore, the motion of the cavity is investigated, revealing that the translational pair (composite) mobility, which linearly couples the velocity of the elastic cavity to the force exerted on the solid particle, is solely determined by membrane shear properties. Our analytical predictions are favorably compared with fully-resolved computer simulations based on a completed-double-layer boundary integral method.

physics.flu-dyn↗

arXiv2019

Clustering-induced velocity-reversals of active colloids mixed with passive particles

Recent experiments have shown that colloidal suspensions can spontaneously self-assemble into dense clusters of various internal structures, sizes and dynamical properties when doped with active Janus particles. Characteristically, these clusters move ballistically during their formation, but dynamically revert their velocity and temporarily move opposite to the self-propulsion direction of the Janus particles they contain. Here we explore a simple effective model of colloidal mixtures which allows reproducing most aspects seen in experiments, including the morphology and the velocity-reversal of the clusters. We attribute the latter to the nonreciprocal phoretic attractions of the passive particles to the active colloids' caps, taking place even at close contact and pushing the active particles backwards. When the phoretic interactions are repulsive, in turn, they cause dynamical aggregation of passive colloids in the chemical density minima produced by the active particles, as recently seen in experiments; in other parameter regimes they induce travelling fronts of active particles pursued by passive ones coexisting with an active gas.

cond-mat.soft↗

arXiv2019

Traveling band formation in feedback-driven colloids

Using simulation and theory we study the dynamics of a colloidal suspension in two dimensions subject to a time-delayed repulsive feedback that depends on the positions of the colloidal particles. The colloidal particles experience an additional potential that is a superposition of repulsive potential energies centered around the positions of all the particles a delay time ago. Here we show that such a feedback leads to self-organization of the particles into traveling bands. The width of the bands and their propagation speed can be tuned by the delay time and the range of the imposed repulsive potential. The emerging traveling band behavior is observed in Brownian dynamics computer simulations as well as microscopic dynamic density functional theory (DDFT). Traveling band formation also persists in systems of finite size leading, in the case of circularly confined systems, to rotating traveling waves.

cond-mat.soft↗

arXiv2019

Multi-species dynamical density functional theory for microswimmers: derivation, orientational ordering, trapping potentials, and shear cells

Microswimmers typically operate in complex environments. In biological systems, often diverse species are simultaneously present and interact with each other. Here, we derive a (time-dependent) particle-scale statistical description, namely a dynamical density functional theory, for such multi-species systems, extending existing works on one-component microswimmer suspensions. In particular, our theory incorporates the effect of external potentials, but also steric and hydrodynamic interactions between swimmers. For the latter, a previously introduced force-dipole-based minimal (pusher or puller) microswimmer model is used. As a limiting case of our theory, mixtures of hydrodynamically interacting active and passive particles are captured as well. After deriving the theory, we apply it to different planar swimmer configurations. First, these are binary pusher--puller mixtures in external traps. In the considered situations, we find that the majority species imposes its behavior on the minority species. Second, for unconfined binary pusher--puller mixtures, the linear stability of an orientationally disordered state against the emergence of global polar orientational order (and thus emergent collective motion) is tested analytically. Our statistical approach predicts, qualitatively in line with previous particle-based computer simulations, a threshold for the fraction of pullers and for their propulsion strength that lets overall collective motion arise. Third, we let driven passive colloidal particles form the boundaries of a shear cell, with confined active microswimmers on their inside. Driving the passive particles then effectively imposes shear flows, which persistently acts on the inside microswimmers. Their resulting behavior reminds of the one of circle swimmers, though with varying swimming radii.

cond-mat.soft↗

arXiv2019

Binary pusher-puller mixtures of active microswimmers and their collective behavior

Microswimmers are active particles of microscopic size that self-propel by setting the surrounding fluid into motion. According to the kind of far-field fluid flow that they induce, they are classified into pushers and pullers. Many studies have explored similarities and differences between suspensions of either pushers or pullers, but the behavior of mixtures of the two is still to be investigated. Here, we rely on a minimal discrete microswimmer model, particle-resolved, including hydrodynamic interactions, to examine the orientational ordering in such binary pusher-puller mixtures. In agreement with existing literature, we find that our monodisperse suspensions of pushers do not show alignment, whereas those of solely pullers spontaneously develop ordered collective motion. By continuously varying the composition of the binary mixtures, starting from pure puller systems, we find that ordered collective motion is largely maintained up to pusher-puller composition ratios of about 1:2. Surprisingly, pushers when surrounded by a majority of pullers are more tightly aligned than indicated by the average overall orientational order in the system. Our study outlines how orientational order can be tuned in active microswimmer suspensions to a requested degree by doping with other species.

cond-mat.soft↗

arXiv2019

Stimuli-responsive behavior of PNiPAm microgels under interfacial confinement

The volume phase transition of microgels is one of the most paradigmatic examples of stimuli-responsiveness, enabling a collapse from a highly swollen microgel state into a densely coiled state by an external stimulus. Although well characterized in bulk, it remains unclear how the phase transition is affected by the presence of a confining interface. Here, we demonstrate that the temperature-induced volume phase transition of poly(N-isopropylacrylamide) microgels, conventionally considered an intrinsic molecular property of the polymer, is in fact largely suppressed when the microgel is adsorbed to an air/liquid interface. We further observe a hysteresis in core morphology and interfacial pressure between heating and cooling cycles. Our results, supported by molecular dynamics simulations, reveal that the dangling polymer chains of microgel particles, spread at the interface under the influence of surface tension, do not undergo any volume phase transition, demonstrating that the balance in free energy responsible for the volume phase transition is fundamentally altered by interfacial confinement. These results imply that important technological properties of such systems, including the temperature-induced destabilization of emulsions does not occur via a decrease in interfacial coverage of the microgels.

cond-mat.soft↗

arXiv2019

Crystallization seeds favour crystallization only during initial growth

Crystallization represents the prime example of a disorder order transition. In realistic situations, however, container walls and impurities are frequently present and hence crystallization is heterogeneously seeded. Rarely the seeds are perfectly compatible with the thermodynamically favoured crystal structure and thus induce elastic distortions, which impede further crystal growth. Here we use a colloidal model system, which not only allows us to quantitatively control the induced distortions but also to visualize and follow heterogeneous crystallization with single-particle resolution. We determine the sequence of intermediate structures by confocal microscopy and computer simulations, and develop a theoretical model that describes our findings. The crystallite first grows on the seed but then, on reaching a critical size, detaches from the seed. The detached and relaxed crystallite continues to grow, except close to the seed, which now prevents crystallization. Hence, crystallization seeds facilitate crystallization only during initial growth and then act as impurities.

cond-mat.soft↗

arXiv2019

Propagating Density Spikes in Light-Powered Motility-Ratchets

Combining experiments and computer simulations, we use a spatially periodic and flashing light-field to direct the motion of phototactic active colloids. Here, the colloids self-organize into a density spike pattern, which resembles a shock wave and propagates over long distances, almost without dispersing. The underlying mechanism involves a synchronization of the colloids with the light-field, so that particles see the same intensity gradient each time the light-pattern is switched on, but no gradient in between (for example). This creates a pulsating transport whose strength and direction can be controlled via the flashing protocol and the self-propulsion speed of the colloids. Our results might be useful for drug delivery applications and can be used to segregate active colloids by their speed.

cond-mat.soft↗

arXiv2019

Motility-induced temperature difference in coexisting phases

In nature, objects which are in thermal contact with each other, usually approach the same temperature, unless a heat source (or sink) cherishes a persistent flow of heat. Accordingly, in a well-isolated apartment flat, most items are at a similar temperature. This is a general consequence of equilibrium thermodynamics, requiring coexisting phases to have identical temperatures. Opposing this generic situation, here we identify a system showing different temperatures in coexisting phases, which are separated from each other by a sharp and persistent temperature gradient. Thermodynamically, such a "hot" and a "cold" phase are allowed to coexist, as the system we consider comprises "active" particles which self-propel relative to their environment and are thus intrinsically out-of-equilibrium. Although these microparticles are well known to spontaneously phase-separate into a liquid- and a gas-like state, different kinetic temperatures in coexisting phases occur if and only if inertia is introduced, which is neglected in standard models describing active particles. Our results, therefore, exemplify a novel route to use active particles to create a self-sustained temperature gradient across coexisting phases, a phenomenon, which is fundamentally beyond equilibrium physics.

cond-mat.soft↗

arXiv2019

Active particles in non-inertial frames: how to self-propel on a carousel

Typically the motion of self-propelled active particles is described in a quiescent environment establishing an inertial frame of reference. Here we assume that friction, self-propulsion and uctuations occur relative to a non-inertial frame and thereby the active Brownian motion model is generalized to non-inertial frames. First, analytical solutions are presented for the overdamped case, both for linear swimmers and circle swimmers. For a frame rotating with constant angular velocity ("carousel"), the resulting noise-free trajectories in the static laboratory frame trochoids if these are circles in the rotating frame. For systems governed by inertia, such as vibrated granulates or active complex plasmas, centrifugal and Coriolis forces become relevant. For both linear and circling self-propulsion, these forces lead to out-spiraling trajectories which for long times approach a spira mirabilis. This implies that a self-propelled particle will typically leave a rotating carousel. A navigation strategy is proposed to avoid this expulsion, by adjusting the self-propulsion direction at wish. For a particle, initially quiescent in the rotating frame, it is shown that this strategy only works if the initial distance to the rotation centre is smaller than a critical radius Rc which scales with the self-propulsion velocity. Possible experiments to verify the theoretical predictions are discussed.

cond-mat.soft↗

arXiv2019

Classical density functional theory for a two-dimensional isotropic ferrogel model with labeled particles

In this study, we formulate a density functional theory (DFT) for systems of labeled particles, considering a two-dimensional bead-spring lattice with a magnetic dipole on every bead as a model for ferrogels. On the one hand, DFT has been widely studied to investigate fluid-like states of materials, in which constituent particles are not labeled as they can exchange their positions without energy cost. On the other hand, in ferrogels consisting of magnetic particles embedded in elastic polymer matrices, the particles are labeled by their positions as their neighbors do not change over time. We resolve such an issue of particle labeling, introducing a mapping of the elastic interaction mediated by the springs onto a pairwise additive interaction (pseudo-springs) between unlabeled particles. We further investigate magnetostriction and changes in the elastic constants under altered magnetic interactions employing the pseudo-spring potential. It is revealed that there are two different response scenarios in the mechanical properties of the dipole-spring systems: while systems at low packing fractions are hardened as the magnetic moments increase in magnitude, at high packing fractions softening due to diminishing effects from the steric force, associated with increases in the volume, is observed. Validity of the theory is also verified by Monte-Carlo simulations with both real and pseudo-springs. We expect that our DFT approach may shed light on an understanding of materials with particle inclusions.

cond-mat.soft↗

arXiv2019

Axisymmetric flow due to a Stokeslet near a finite-sized elastic membrane

Elastic confinements play an important role in many soft matter systems and affect the transport properties of suspended particles in viscous flow. On the basis of low-Reynolds-number hydrodynamics, we present an analytical theory of the axisymmetric flow induced by a point-force singularity (Stokeslet) directed along the symmetry axis of a finite-sized circular elastic membrane endowed with resistance toward shear and bending. The solution for the viscous incompressible flow surrounding the membrane is formulated as a mixed boundary value problem, which is then reduced into a system of dual integral equations on the inner and outer sides of the domain boundary. We show that the solution of the elastohydrodynamic problem can conveniently be expressed in terms of a set of inhomogeneous Fredholm integral equations of the second kind with logarithmic kernel. Basing on the hydrodynamic flow field, we obtain semi-analytical expressions of the hydrodynamic mobility function for the translational motion perpendicular to a circular membrane. The results are valid to leading-order in the ratio of particle radius to the distance separating the particle from the membrane. In the quasi-steady limit, we find that the particle mobility near a finite-sized membrane is always larger than that predicted near a no-slip disk of the same size. We further show that the bending-related contribution to the hydrodynamic mobility increases monotonically upon decreasing the membrane size, whereas the shear-related contribution displays a minimum value when the particle-membrane distance is equal to the membrane radius. Accordingly, the system behavior may be shear or bending dominated, depending on the geometric and elastic properties of the system. Our results may find applications in the field of nanoparticle-based sensing and drug delivery systems near elastic cell membranes.

physics.flu-dyn↗

arXiv2019

Colloidal Brazil nut effect in microswimmer mixtures induced by motility contrast

We numerically and experimentally study the segregation dynamics in a binary mixture of microswimmers which move on a two-dimensional substrate in a static periodic triangular-like light intensity field. The motility of the active particles is proportional to the imposed light intensity and they possess a motility contrast, i.e., the prefactor depends on the species. In addition, the active particles also experience a torque aligning their motion towards the direction of the negative intensity gradient. We find a segregation of active particles near the intensity minima where typically one species is localized close to the minimum and the other one is centered around in an outer shell. For a very strong aligning torque, there is an exact mapping onto an equilibrium system in an effective external potential that is minimal at the intensity minima. This external potential is similar to (height-dependent) gravity, such that one can define effective `heaviness' of the self-propelled particles. In analogy to shaken granular matter in gravity, we define a `colloidal Brazil nut effect' if the heavier particles are floating on top of the lighter ones. Using extensive Brownian dynamics simulations, we identify system parameters for the active colloidal Brazil nut effect to occur and explain it based on a generalized Archimedes' principle within the effective equilibrium model: heavy particles are levitated in a dense fluid of lighter particles if their effective mass density is lower than that of the surrounding fluid. We also perform real-space experiments on light-activated self-propelled colloidal mixtures which confirm the theoretical predictions.

cond-mat.soft↗

arXiv2019

Optimal Control Strategies for Active Particle Navigation

The quest for the optimal navigation strategy in a complex environment is at the heart of microswimmer applications like cargo carriage or drug targeting to cancer cells. Here, we formulate a variational Fermat's principle for microswimmers determining the optimal path regarding travelling time, energy dissipation or fuel consumption. For piecewise constant forces (or flow fields), the principle leads to Snell's law, showing that the optimal path is piecewise linear, as for light rays, but with a generalized refraction law. For complex environments, like general 1D-, shear- or vortex-fields, we obtain exact analytical expressions for the optimal path, showing, for example, that microswimmers sometimes have to temporarily navigate away from their target to reach it fastest. Our results might be useful to benchmark algorithmic schemes for optimal navigation.

cond-mat.soft↗

arXiv2019

Membrane penetration and trapping of an active particle

The interaction between nano- or micro-sized particles and cell membranes is of crucial importance in many biological and biomedical applications such as drug and gene delivery to cells and tissues. During their cellular uptake, the particles can pass through cell membranes via passive endocytosis or by active penetration to reach a target cellular compartment or organelle. In this manuscript, we develop a simple model to describe the interaction of a self-driven spherical particle (moving through an effective constant active force) with a minimal membrane system, allowing for both penetration and trapping. We numerically calculate the state diagram of this system, the membrane shape, and its dynamics. In this context, we show that the active particle may either get trapped near the membrane or penetrates through it, where the membrane can either be permanently destroyed or recover its initial shape by self-healing. Additionally, we systematically derive a continuum description allowing to accurately predict most of our results analytically. This analytical theory helps identifying the generic aspects of our model, suggesting that most of its ingredients should apply to a broad range of membranes, from simple model systems composed of magnetic microparticles to lipid bilayers. Our results might be useful to predict mechanical properties of synthetic minimal membranes.

cond-mat.soft↗

arXiv2018

Light-controlled Assembly of Active Colloidal Molecules

Thanks to a constant energy input, active matter can self-assemble into phases with complex architectures and functionalities such as living clusters that dynamically form, reshape and break-up, which are forbidden in equilibrium materials by the entropy maximization (or free energy minimization) principle. The challenge to control this active self-assembly has evoked widespread efforts typically hinging on engineering of the properties of individual motile constituents. Here, we provide a different route, where activity occurs as an emergent phenomenon only when individual building blocks bind together in a way that we control by laser light. Using experiments and simulations of two species of immotile microspheres, we exemplify this route by creating active molecules featuring a complex array of behaviors, becoming migrators, spinners and rotators. The possibility to control the dynamics of active self-assembly via light-controllable nonreciprocal interactions will inspire new approaches to understand living matter and to design active materials.

cond-mat.soft↗