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We consider a nanodimer in solution with asymmetric thermal properties that shows self-propelled motion. One monomer of the nanodimer can be heated to a fixed temperature producing a radially symmetric temperature gradient. The thermophoretic properties of the second monomer produce then a propulsion against or toward the heated particle, such that the nanodimer becomes a puller or pusher nanoswimmer. We combine our simulation measurements with a theoretical analysis that satisfactorily characterizes the self-propelled velocity with the temperature gradient, and the thermophoretic properties of the bead. [ABSTRACT FROM AUTHOR]

We perform optical-tweezers experiments and mesoscale fluid simulations to study the effective interactions between two parallel plates immersed in bacterial suspensions. The plates are found to experience a long-range attraction, which increases linearly with bacterial density and decreases with plate separation. The higher bacterial density and orientation order between plates observed in the experiments imply that the long-range effective attraction mainly arises from the bacterial flow field, instead of the direct bacterium-plate collisions, which is confirmed by the simulations. Furthermore, the hydrodynamic contribution is inversely proportional to the squared interplate separation in the far field. Our findings highlight the importance of hydrodynamics on the effective forces between passive objects in active baths, providing new possibilities to control activity-directed assembly.

We construct structural order parameters based on local angular and radial distribution functions in dense colloidal suspensions. All the order parameters show significant correlations to local dynamics in the supercooled and glass regime. In particular, the correlations between the orientational order and dynamical heterogeneity are consistently higher than those between the conventional two-body structural entropy and local dynamics. The structure-dynamics correlations can be explained by a excitation model with the energy barrier depending on local structural order. Our results suggest that in dense disordered packings, local orientational order is higher than translational order, and plays a more important role in determining the dynamics in glassy systems.

Using video microscopy, we measure the long-time diffusion coefficients of colloidal particles at different concentrations. The measured diffusion coefficients start to deviate from theoretical predictions based on random collision models upon entering the supercooled regime. The theoretical diffusion relation is recovered by assigning an effective mass proportional to the size of structurally correlated clusters to the diffusing particles, providing an indirect method to probe the growth of static correlation length scales approaching the glass transition. This method is tested and validated in the crystallization of mono-disperse colloids in quasi-two-dimensional experiments. The correlation length obtained for a binary colloidal liquid increases by a power law toward a critical packing fraction of ∼0.79. The system relaxation time exhibits a power-law dependence on the correlation length in agreement with dynamical facilitation theories.

We perform experiments and computer simulations to study the effective interactions between like-charged colloidal tracers moving in a two-dimensional fluctuating background of colloidal crystal. By a counting method that properly accounts for the configurational degeneracy of tracer pairs, we extract the relative probability of finding a tracer pair in neighboring triangular cells formed by background particles. We find that this probability at the nearest neighbor cell is remarkably greater than those at cells with larger separations, implying an effective attraction between the tracers. This effective attraction weakens sharply as the background lattice constant increases. Furthermore, we clarify that the lattice-mediated effective attraction originates from the minimization of free energy increase from deformation of the crystalline background due to the presence of diffusing tracers.

The discovery of topological edge states that unidirectionally propagate along the boundary of system without backscattering has enabled the development of new design principles for material or information transport. Here, we show that the topological edge flow supported by the chiral active fluid composed of spinners can even robustly transport an immersed intruder with the aid of the spinner-mediated depletion interaction between the intruder and boundary. Importantly, the effective interaction significantly depends on the dissipationless odd viscosity of the chiral active fluid, which originates from the spinning-induced breaking of time-reversal and parity symmetries, rendering the transport controllable. Our findings propose a novel avenue for robust cargo transport and could open a range of new possibilities throughout biological and microfluidic systems.

Using video microscopy and simulations, we study the long-time diffusion of colloidal tracers in a wide range of model porous media composed of frozen colloidal matrices with different structures. We found that the diffusion coefficient of a tracer can be quantitatively determined by the structures of porous media. In particular, a universal scaling relation exists between the dimensionless diffusion coefficient of the tracer and the structural entropy of the system. This universal scaling relation is an extension of the scaling law previously discovered for the diffusion of colloidal particles in fluctuating media.

Using simulations and experiments, we demonstrate that the effective interaction between passive particles in an active bath substantially depends on an external constraint suffered by the passive particles. Particularly, the effective interaction between two free passive particles, which is directly measured in simulation, is qualitatively different from the one between two fixed particles. Moreover, we find that the friction experienced by the passive particles-a kinematic constraint-similarly influences the effective interaction. These remarkable features are in significant contrast to the equilibrium cases, and mainly arise from the accumulation of the active particles near the concave gap formed by the passive spheres. This constraint dependence not only deepens our understanding of the "active depletion force," but also provides an additional tool to tune the effective interactions in an active bath.

Using video microscopy and simulations, we study the diffusion of probe particles in a wide range of complex backgrounds, both crystalline and disordered, in quasi-2D colloidal systems. The dimensionless diffusion coefficients D^{*} from different systems collapse to a single master curve when plotted as a function of the structural entropy of the backgrounds, confirming the universal relation between diffusion dynamics and the structure of the medium. A new scaling equation is proposed with consideration for the viscous friction from the solvent, which is absent in previous theoretical models. This new universal law quantitatively predicts the diffusion coefficients from different systems over several orders of magnitude of D^{*}, with a single common fitting parameter.

Using an event-driven molecular dynamics simulation, we show that simple monodisperse granular beads confined in coupled columns may oscillate as a different type of granular clock. To trigger this oscillation, the system needs to be driven against gravity into a density-inverted state, with a high-density clustering phase supported from below by a gaslike low-density phase (Leidenfrost effect) in each column. Our analysis reveals that the density-inverted structure and the relaxation dynamics between the phases can amplify any small asymmetry between the columns, and lead to a giant oscillation. The oscillation occurs only for an intermediate range of the coupling strength, and the corresponding phase diagram can be universally described with a characteristic height of the density-inverted structure. A minimal two-phase model is proposed and a linear stability analysis shows that the triggering mechanism of the oscillation can be explained as a switchable two-parameter Andronov-Hopf bifurcation. Numerical solutions of the model also reproduce similar oscillatory dynamics to the simulation results.

We image local structural rearrangements in soft colloidal glasses under small periodic perturbations induced by thermal cycling. Local structural entropy S_{2} positively correlates with observed rearrangements in colloidal glasses. The high S_{2} values of the rearranging clusters in glasses indicate that fragile regions in glasses are structurally less correlated, similar to structural defects in crystalline solids. Slow-evolving high S_{2} spots are capable of predicting local rearrangements long before the relaxations occur, while fluctuation-created high S_{2} spots best correlate with local deformations right before the rearrangement events. Local free volumes are also found to correlate with particle rearrangements at extreme values, although the ability to identify relaxation sites is substantially lower than S_{2}. Our experiments provide an efficient structural identifier for the fragile regions in glasses and highlight the important role of structural correlations in the physics of glasses.

In contrast to most real fluids, angular momentum is not a locally conserved quantity in some mesoscopic simulation methods. Here we quantify the importance of this conservation in the flow fields associated with different colloidal systems. The flow field is analytically calculated with and without angular momentum conservation for the multiparticle collision dynamics (MPC) method, and simulations are performed to verify the predictions. The flow field generated around a colloidal particle moving under an external force with slip boundary conditions depends on the conservation of angular momentum, and the amplitude of the friction force is substantially affected. Interestingly, no dependence on the angular momentum conservation is found for the flow fields generated around colloids under the influence of phoretic forces. Moreover, circular Couette flow between a no-slip and a slip cylinder is investigated, which allows us to validate one of the two existing expressions for the MPC stress tensor.

The Langevin description of Brownian motion in inhomogeneous suspensions is here revisited. Inhomogeneous suspensions are characterized by a position-dependent friction coefficient, which can significantly influence the dynamics of the suspended particles. Outstanding examples are suspensions in confinement or in the presence of a temperature gradient. The Langevin approach in inhomogeneous systems encounters a fundamental difficulty related to the interpretation of the multiplicative noise induced by the position-dependent friction. We show that the so-called Ito-Stratonovich dilemma is originated by the violation of the macroscopic force balance condition in the traditional procedure of eliminating the fast variables. Repairing this deficit, we rederive the extended overdamped Langevin equation directly from the infradamped Langevin equation. This is without invoking the Fokker-Planck formalism, such that the self-completeness of the Langevin framework is restored. Furthermore, we derive the generalized forms of the drift-force relation and the Smoluchowski equation for inhomogeneous suspensions in a straightforward manner.

A general Monte Carlo simulation method of calculating the elastic constants of a polydisperse hard-sphere colloidal crystal is developed. Elastic constants of a size-polydisperse hard-sphere fcc crystal are calculated. The pressure and three elastic constants ( C11, C12, and C44 ) increase significantly with the polydispersity. It was also found from extrapolation that there is a mechanical terminal polydispersity above which a fcc crystal will be mechanically unstable.