Using evaporation to control capillary instabilities in micro-systems.

The instabilities of fluid interfaces represent both a limitation and an opportunity for the fabrication of small-scale devices. Just as non-uniform capillary pressures can destroy micro-electrical mechanical systems (MEMS), so they can guide the assembly of novel solid and fluid structures. In many such applications the interface appears during an evaporation process and is therefore only present temporarily. It is commonly assumed that this evaporation simply guides the interface through a sequence of equilibrium configurations, and that the rate of evaporation only sets the timescale of this sequence. Here, we use Lattice-Boltzmann simulations and a theoretical analysis to show that, in fact, the rate of evaporation can be a factor in determining the onset and form of dynamical capillary instabilities. Our results shed light on the role of evaporation in previous experiments, and open the possibility of exploiting diffusive mass transfer to directly control capillary flows in MEMS applications.

Collective and convective effects compete in patterns of dissolving surface droplets.

The effects of neighboring droplets on the dissolution of a sessile droplet, i.e. collective effects, are investigated both experimentally and numerically. On the experimental side small approximately 20 nL mono-disperse surface droplets arranged in an ordered pattern were dissolved and their size evolution is studied optically. The droplet dissolution time was studied for various droplet patterns. On the numerical side, lattice-Boltzmann simulations were performed. Both simulations and experiments show that the dissolution time of a droplet placed in the center of a pattern can increase by as much as 60% as compared to a single, isolated droplet, due to the shielding effect of the neighboring droplets. However, the experiments also show that neighboring droplets enhance the buoyancy driven convective flow of the bulk, increasing the mass exchange and counteracting collective effects. We show that this enhanced convection can reduce the dissolution time of droplets at the edges of the pattern to values below that of a single, isolated droplet.

Dynamics of a homogeneous active dumbbell system.

We analyze the dynamics of a two-dimensional system of interacting active dumbbells. We characterize the mean-square displacement, linear response function, and deviation from the equilibrium fluctuation-dissipation theorem as a function of activity strength, packing fraction, and temperature for parameters such that the system is in its homogeneous phase. While the diffusion constant in the last diffusive regime naturally increases with activity and decreases with packing fraction, we exhibit an intriguing nonmonotonic dependence on the activity of the ratio between the finite-density and the single-particle diffusion constants. At fixed packing fraction, the time-integrated linear response function depends nonmonotonically on activity strength. The effective temperature extracted from the ratio between the integrated linear response and the mean-square displacement in the last diffusive regime is always higher than the ambient temperature, increases with increasing activity, and, for small active force, monotonically increases with density while for sufficiently high activity it first increases and next decreases with the packing fraction. We ascribe this peculiar effect to the existence of finite-size clusters for sufficiently high activity and density at the fixed (low) temperatures at which we worked. The crossover occurs at lower activity or density the lower the external temperature. The finite-density effective temperature is higher (lower) than the single dumbbell one below (above) a crossover value of the Péclet number.