New electric-field-driven mesoscale phase transitions in polarized suspensions.

We report the discovery of a new class of an electric field-driven bulk phase transition due solely to dipolar interactions in a suspension under the action of a uniform ac field where the effects of other competing forces are suppressed. This transition appears after the well-known chain-column formation and causes the uniform suspension of columns to rearrange into a cellular pattern consisting of particle-free domains surrounded by particle-rich walls. Interestingly, the characteristic size of these domains scales linearly with the interelectrode spacing and remains insensitive to the size of the particles.

Hysteresis, force oscillations, and nonequilibrium effects in the adhesion of spherical nanoparticles to atomically smooth surfaces.

Equilibrium and nonequilibrium aspects of particle adsorption on the walls of fluid-filled nanochannels are examined via molecular dynamics simulations. The force on the particle and the free energy of the system are found to depend on the particle's history (hysteresis), in addition to its radial position and the wetting properties of the fluid, even when the particle moves quasistatically. The hysteresis is associated with changes in the fluid density in the gap between the particle and the wall, which persist over surprisingly long times.

Combined negative dielectrophoresis and phase separation in nondilute suspensions subject to a high-gradient ac electric field.

Experiments were conducted on concentrated suspensions of neutrally buoyant particles which exhibit negative dielectrophoresis. We found that, due to interparticle electrical interactions, such suspensions undergo a phase separation when subjected to a high-gradient ac field (approximately kV/mm) and form a propagating distinct front between the regions enriched with and depleted of particles. A generalization of our theory for the thermodynamics of the field-induced phase transitions in suspensions of polarized particles [Phys.

Adsorption phenomena in the transport of a colloidal particle through a nanochannel containing a partially wetting fluid.

Using molecular dynamics simulations, we study the motion of a closely fitting nanometer-size solid sphere in a fluid-filled cylindrical nanochannel at low Reynolds numbers. At early times, when the particle is close to the middle of the tube, its velocity is in agreement with continuum calculations, despite large thermal fluctuations. At later times, partially wetting fluids exhibit novel adsorption phenomena: the sphere meanders away from the center of the tube and adsorbs onto the wall, and subsequently either sticks to the wall and remains motionless on average, or separates slightly from the tube wall and then either slips parallel to the mean flow or executes an intermittent stick-slip motion.