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Register a new userSelf-Assembly and Nonlinear Dynamics of Dimeric Colloidal Rotors in Cholesterics
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We study by simulation the physics of two colloidal particles in a cholesteric liquid crystal with tangential order parameter alignment at the particle surface. The effective force between the pair is attractive at short range and favors assembly of colloid dimers at specific orientations relative to the local director field. When pulled through the fluid by a constant force along the helical axis, we find that such a dimer rotates, either continuously or stepwise with phase-slip events. These cases are separated by a sharp dynamical transition and lead, respectively, to a constant or an ever-increasing phase lag between the dimer orientation and the local nematic director.
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This article explores the governing role of the internal hydrodynamics and advective transport within sessile colloidal droplets on the self assembly of nanostructures to form floral patterns. Water acetone binary fluid and Bi2O3 nanoflakes based complex fluids are experimented with. Microliter sessile droplets are allowed to vaporize and the dry out patterns are examined using scanning electron microscopy. The presence of distributed self assembled rose like structures is observed. The population density, structure and shape of the floral structures are noted to be dependent on the binary fluid composition and nanomaterial concentration. Detailed microscopic particle image velocimetry analysis is undertaken to qualitatively and quantitatively describe the solutal Marangoni advection within the evaporating droplets. It has been shown that the kinetics, regime and location of the internal advection are responsible factors towards the hydrodynamics influenced clustering, aggregation and self-assembly of the nanoflakes. In addition, the size of the nanostructures and the complex fluids.
We investigate the collective motion of magnetic rotors suspended in a viscous fluid under an uniform rotating magnetic field. The rotors are positioned on a square lattice, and low Reynolds hydrodynamics is assumed. For a $3 times 3$ array of magnets, we observe three characteristic dynamical patterns as the external field strength is varied: a synchronized pattern, an oscillating pattern, and a chessboard pattern. The relative stability of these depends on the competition between the energy due to the external magnetic field and the energy of the magnetic dipole-dipole interactions among the rotors. We argue that the chessboard pattern can be understood as an alternation in the stability of two degenerate states, characterized by striped and spin-ice configurations, as the applied magnetic field rotates. For larger arrays, we observe propagation of slip waves that are similar to metachronal waves. The rotor arrays have potential as microfluidic devices that can mix fluids and create vortices of different sizes.
Colloidal crystals exhibit structural color without any color pigment due to the crystals periodic nanostructure, which can interfere with visible light. This crystal structure is iridescent as the resulting color changes with the viewing or illumination angle, which limits its use for printing or displays. To eliminate the iridescent property, it is important to make the packing of the colloidal nanoparticles disordered. Here, we introduce a drop-casting method where a droplet of a water- ethanol mixture containing monodisperse polymer-coated silica nanoparticles creates a relatively uniform and non-iridescent deposit after the droplet evaporates completely on a heated substrate. The uniformity is caused by a thermal Marangoni flow and fast evaporation effects due to the heated substrate, whereas non-iridescence is the outcome of short-range-ordered packing of nanoparticles by depletion attraction and friction effects produced by polymer brushes. We show that the colors of the final deposits from individual droplets remain unchanged while the viewing angle is varied under ambient light. We expect that the coating method is compatible with ink-jet printing and the uniformly coated self-assembled non-iridescent nanostructures have potential for color displays using reflection mode and other optical devices.
We outline a basic strategy of how self-propulsion can be used to improve the yield of a typical colloidal self-assembly process. The success of this approach is predicated on the thoughtful design of the colloidal building block as well as how self-propulsion is endowed to the particle. As long as a set of criteria are satisfied, it is possible to significantly increase the rate of self-assembly, and greatly expand the window in parameter space where self-assembly can occur. In addition, we show that by tuning the relative on/off time of the self-propelling force it is possible to modulate the effective speed of the colloids allowing for further optimization of the self-assembly process.
Colloidal particles with strong, short-ranged attractions can form a gel. We simulate this process without and with hydrodynamic interactions (HI), using the lattice-Boltzmann method to account for presence of a thermalized solvent. We show that HI speed up and slow down gelation at low and high volume fractions, respectively. The transition between these two regimes is linked to the existence of a percolating cluster shortly after quenching the system. However, when we compare gels at matched structural age, we find nearly indistinguishable structures with and without HI. Our result explains longstanding, unresolved conflicts in the literature.
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