The spatiotemporal dynamics in systems of active self-propelled particles is controlled by the propulsion mechanism in combination with various direct interactions, such as steric repulsion, hydrodynamics, and chemical fields. Yet, these direct interactions are typically anisotropic, and come in different "flavors", such as spherical and elongated particle shapes for steric repulsion, pusher and puller flow fields for hydrodynamics, etc. The combination of the various aspects is expected to lead to new emergent behavior. However, it is a priori not evident whether shape and hydrodynamics act synergistically or antagonistically to generate motility-induced clustering (MIC) and phase separation (MIPS). We employ a model of prolate spheroidal microswimmers-called squirmers-in quasi-two-dimensional confinement to address this issue by mesoscale hydrodynamic simulations. For comparison, non-hydrodynamic active Brownian particles (ABPs) are considered to elucidate the contribution of hydrodynamic interactions on MIC and MIPS. For spherical particles, the comparison between ABP and hydrodynamic-squirmer ensembles reveals a suppression of MIPS due to hydrodynamic interactions. Yet, our analysis shows that dynamic clusters exist, with a broad size distribution. The fundamental difference between ABPs and squirmers is attributed to an increased reorientation of squirmers by hydrodynamic torques during their collisions. In contrast, for elongated squirmers, hydrodynamics interactions enhance MIPS. The transition to a phase-separated state strongly depends on the nature of the swimmer's flow field -with an increased tendency toward MIPS for pullers, a reduced tendency for pushers. Thus, hydrodynamic interactions show opposing effects on MIPS for spherical and elongated microswimmers. Our results imply that details of the propulsion mechanism of biological microswimmers, like pattern and time dependence of the flagellar beat, may be very important to determine their collective behavior. arXiv:1807.01211v1 [cond-mat.soft]
We propose a hydrodynamic model for a spheroidal microswimmer with two tangential surface velocity modes. This model is analytically solvable and reduces to Lighthill's and Blake's spherical squirmer model in the limit of equal major and minor semi-axes. Furthermore, we present an implementation of such a spheroidal squirmer by means of particle-based mesoscale hydrodynamics simulations using the multiparticle collision dynamics approach. We investigate its properties as well as the scattering of two spheroidal squirmers in a slit geometry. Thereby we find a stable fixed point, where two pullers swim cooperatively forming a wedge-like conformation with a small constant angle.
We investigate the emergent dynamical behavior of hydrodynamically coupled microrotors. The two rotors are confined in a plane and move along circles driven by active forces. The three-dimensional fluid is described by the linearized, time-dependent Navier-Stokes equations instead of the usually adopted Stokes equations. We demonstrate that time-dependent hydrodynamic interactions lead to synchronization of the rotational motion. The time dependence of the phase difference between the rotors is determined and synchronization times are extracted for various external torques and rotor separations by solving the underlaying integrodifferential equations numerically. In addition, an analytical expression is provided for the synchronization time.
The friction and diffusion coefficients of rigid spherical colloidal particles dissolved in a fluid are determined from velocity and force autocorrelation functions by mesoscale hydrodynamic simulations. Colloids with both slip and no-slip boundary conditions are considered, which are embedded in fluids modeled by multiparticle collision dynamics with and without angular momentum conservation. For no-slip boundary conditions, hydrodynamics yields the well-known Stokes law, while for slip boundary conditions the lack of angular momentum conservation leads to a reduction of the hydrodynamic friction coefficient compared to the classical result. The colloid diffusion coefficient is determined by integration of the velocity autocorrelation function, where the numerical result at shorter times is combined with the theoretical hydrodynamic expression for longer times. The suitability of this approach is confirmed by simulations of sedimenting colloids. In general, we find only minor deviations from the Stokes-Einstein relation, which even disappear for larger colloids. Importantly, for colloids with slip boundary conditions, our simulation results contradict the frequently assumed additivity of local and hydrodynamic diffusion coefficients.
We determine the viscosity parameters of the multiparticle collision dynamics (MPC) approach, a particle-based mesoscale hydrodynamic simulation method for fluids. We perform analytical calculations and verify our results by simulations. The stochastic rotation dynamics and the Andersen thermostat variant of MPC are considered, both with and without angular momentum conservation. As an important result, we find a nonzero bulk viscosity for every MPC version. The explicit calculation shows that the bulk viscosity is determined solely by the collisional interactions of MPC.
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