Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userHydrodynamic simulations of self-phoretic microswimmers
77
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
A mesoscopic hydrodynamic model to simulate synthetic self-propelled Janus particles which is thermophoretically or diffusiophoretically driven is here developed. We first propose a model for a passive colloidal sphere which reproduces the correct rotational dynamics together with strong phoretic effect. This colloid solution model employs a multiparticle collision dynamics description of the solvent, and combines potential interactions with the solvent, with stick boundary conditions. Asymmetric and specific colloidal surface is introduced to produce the properties of self-phoretic Janus particles. A comparative study of Janus and microdimer phoretic swimmers is performed in terms of their swimming velocities and induced flow behavior. Self-phoretic microdimers display long range hydrodynamic interactions and can be characterized as pullers or pushers. In contrast, Janus particles are characterized by short range hydrodynamic interactions and behave as neutral swimmers. Our model nicely mimics those recent experimental realization of the self-phoretic Janus particles.
rate research
Read More
The design of artificial microswimmers is often inspired by the strategies of natural microorganisms. Many of these creatures exploit the fact that elasticity breaks the time-reversal symmetry of motion at low Reynolds numbers, but this principle has been notably absent from model systems of active, self-propelled microswimmers. Here we introduce a class of microswimmer that spontaneously self-assembles and swims without using external forces, driven instead by surface phase transitions induced by temperature variations. The swimmers are made from alkane droplets dispersed in aqueous surfactant solution, which start to self-propel upon cooling, pushed by rapidly growing thin elastic tails. When heated, the same droplets recharge by retracting their tails, swimming for up to tens of minutes in each cycle. Thermal oscillations of approximately 5 degrees Celsius induce the swimmers to harness heat from the environment and recharge multiple times. We develop a detailed elastohydrodynamic model of these processes and highlight the molecular mechanisms involved. The system offers a convenient platform for examining symmetry breaking in the motion of swimmers exploiting flagellar elasticity. The mild conditions and biocompatible media render these microswimmers potential probes for studying biological propulsion and interactions between artificial and biological swimmers.
Active systems contain self-propelled particles and can spontaneously self-organize into patterns making them attractive candidates for the self-assembly of smart soft materials. One key limitation of our present understanding of these materials hinges on the complexity of the microscopic mechanisms driving its components forward. Here, by combining experiments, analytical theory and simulations we explore such a mechanism for a class of active system, modular microswimmers, which self-assemble from colloids and ion-exchange resins on charged substrates. Our results unveil the self-assembly processes and the working mechanism of the ion-exchange driven motors underlying modular microswimmers, which have so far been illusive, even qualitatively. We apply these motors to show that modular microswimmers can circumvent corners in complex environments and move uphill. Our work closes a central knowledge gap in modular microswimmers and provides a facile route to extract mechanical energy from ion-exchange processes.
Studies of model microswimmers have significantly contributed to the understanding of the principles of self-propulsion we have today. However, only a small number of microswimmer types have been amenable to analytic modeling, and further development of such approaches is necessary to identify the key features of these active systems. Here we present a general perturbative calculation scheme for swimmers composed of beads interacting by harmonic potentials, driven by an arbitrary force protocol. The hydrodynamic interactions are treated using the Oseen and Rotne-Pragner approximations. We validate our approach by using 3 bead assemblies and comparing the results with the numerically obtained full-solutions of the governing equations of motion, as well as with the existing analytic models for a linear and a triangular swimmer geometries. While recovering the relation between the force and swimming velocity, our detailed analysis and the controlled level of approximation allow us to find qualitative differences already in the far field flow of the devices. Consequently, we are able to identify a behavior of the swimmer that is richer than predicted in previous models. Given its generality, the framework can be applied to any swimmer geometry, driving protocol and beads interactions, as well as in many swimmers problems.
Phoretic particles self-propel using self-generated physico-chemical gradients at their surface. Within a suspension, they interact hydrodynamically by setting the fluid around them into motion, and chemically by modifying the chemical background seen by their neighbours. While most phoretic systems evolve in confined environments due to buoyancy effects, most models focus on their interactions in unbounded flows. Here, we propose a first model for the interaction of phoretic particles in Hele-Shaw confinement and show that in this limit, hydrodynamic and phoretic interactions share not only the same scaling but also the same form, albeit in opposite directions. In essence, we show that phoretic interactions effectively reverse the sign of the interactions that would be obtained for swimmers interacting purely hydrodynamically. Yet, hydrodynamic interactions can not be neglected as they significantly impact the magnitude of the interactions. This model is then used to analyse the behaviour of a suspension. The suspension exhibits swirling and clustering collective modes dictated by the orientational interactions between particles, similar to hydrodynamic swimmers, but here governed by the surface properties of the phoretic particle; the reversal in the sign of the interaction tends to slow down the swimming motion of the particles.
We numerically investigate the motion of active artificial microswimmers diffusing in a fuel concentration gradient. We observe that, in the steady state, their probability density accumulates in the low-concentration regions, whereas a tagged swimmer drifts with velocity depending in modulus and orientation on how the concentration gradient affects the self-propulsion mechanism. Under most experimentally accessible conditions, the particle drifts toward the high-concentration regions (pseudo-chemotactic drift). A correct interpretation of experimental data must account for such an anti-Fickian behavior.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
