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Register a new userDynamics of Colloidal Cubes and Cuboids in Cylindrical Nanopores
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Understanding how colloidal suspensions behave in confined environments has a striking relevance in practical applications. Despite the fact that the behaviour of colloids in the bulk is key to identify the main elements affecting their equilibrium and dynamics, it is only by studying their response under confinement that one can ponder the use of colloids in formulation technology. In particular, confining fluids of anisotropic particles in nanopores provides the opportunity to control their phase behaviour and stabilise a spectrum of morphologies that cannot form in the bulk. By properly selecting pore geometry, particle architecture and system packing, it is possible to tune thermodynamic, structural and dynamical properties for ad hoc applications. In the present contribution, we report Grand Canonical and Dynamic Monte Carlo simulations of suspensions of colloidal cubes and cuboids constrained into cylindrical nanopores of different size. We first study their phase behaviour, calculate the chemical potential vs density equation of state and characterise the effect of the pore walls on particle anchoring and layering. In particular, at large enough concentrations, we observe the formation of concentric nematic-like coronas of oblate or prolate particles surrounding an isotropic core, whose features resemble those typically detected in the bulk. We then analyse the main characteristics of their dynamics and discover that these are dramatically determined by the ability of particles to diffuse in the longitudinal and radial direction of the nanopore.
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Macromolecular diffusion in dense colloidal suspensions is an intriguing topic of interdisciplinary relevance in Science and Engineering. While significant efforts have been undertaken to establish the impact of crowding on the dynamics of macromolecules, less clear is the role played by long-range ordering. In this work, we perform Dynamic Monte Carlo simulations to assess the importance of ordered crowding on the diffusion of globular macromolecules, here modelled as spherical tracers, in suspensions of colloidal cuboids. We first investigate the diffusion of such guest tracers in very weakly ordered host phases of cuboids and, by increasing density above the isotropic-to-nematic phase boundary, study the influence of long-range orientational ordering imposed by the occurrence of liquid-crystalline phases. To this end, we analyse a spectrum of dynamical properties that clarify the existence of slow and fast tracers and the extent of deviations from Gaussian behaviour. Our results unveil the existence of randomly oriented clusters of cuboids that display a relatively large size in dense isotropic phases, but are basically absent in the nematic phase. We believe that these clusters are responsible for a pronounced non-Gaussian dynamics that is much weaker in the nematic phase, where orientational ordering smooths out such structural heterogeneities.
Using grand canonical Monte Carlo simulations, we have explored the phenomenon of capillary condensation (CC) of Ar at the triple temperature inside infinitely long, cylindrical pores. Pores of radius R= 1 nm, 1.7 nm and 2.5 nm have been investigated, using a gas-surface interaction potential parameterized by the well-depth D of the gas on a planar surface made of the same material as that comprising the porous host. For strongly attractive situations, i.e., large D, one or more (depending on R) Ar layers adsorb successively before liquid fills the pore. For very small values of D, in contrast, negligible adsorption occurs at any pressure P below saturated vapor pressure P0; above saturation, there eventually occurs a threshold value of P at which the coverage jumps from empty to full, nearly discontinuously. Hysteresis is found to occur in the simulation data whenever abrupt CC occurs, i.e. for R>= 1.7 nm, and for small D when R=1nm. Then, the pore-emptying branch of the adsorption isotherm exhibits larger N than the pore-filling branch, as is known from many experiments and simulation studies. The relation between CC and wetting on planar surfaces is discussed in terms of a threshold value of D, which is about one-half of the value found for the wetting threshold on a planar surface. This finding is consistent with a simple thermodynamic model of the wetting transition developed previously.
Field-induced reorientation of colloidal particles is especially relevant to manipulate the optical properties of a nanomaterial for target applications. We have recently shown that surprisingly feeble external stimuli are able to transform uniaxial nematic liquid crystals (LCs) of cuboidal particles into biaxial nematic LCs. In the light of these results, here we apply an external field that forces the reorientation of colloidal cuboids in nematic LCs and sparks a uniaxial-to-biaxial texture switching. By Dynamic Monte Carlo simulation, we investigate the unsteady-state reorientation dynamics at the particle scale when the field is applied (uniaxial-to-biaxial switching) and then removed (biaxial-to-uniaxial switching). We detect a strong correlation between the response time, being the time taken for the system to reorient, and particle anisotropy, which spans from rod-like to plate-like geometries. Interestingly, self-dual shaped cuboids, theoretically considered as the most suitable to promote phase biaxiality for being exactly in between prolate and oblate particles, exhibit surprisingly slow response times, especially if compared to prolate cuboids.
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.
We report results of dynamic light scattering measurements of the coherent intermediate scattering function (ISF) of glasses of hard spheres for several volume fractions and a range of scattering vectors around the primary maximum of the static structure factor. The ISF shows a clear crossover from an initial fast decay to a slower non-stationary decay. Ageing is quantified in several different ways. However, regardless of the method chosen, the perfect aged glass is approached in a power-law fashion. In particular, the coupling between the fast and slow decays, as measured by the degree of stretching of the ISF at the crossover, also decreases algebraically with waiting time. The non-stationarity of this coupling implies that even the fastest detectable processes are themselves non-stationary.
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