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Kritika Kritika

Publications and source records attributed to Kritika Kritika.

2 recordsLinked to original sources

Controlling Porosity in Supraparticles Composed of Colloidal Rods and Spheres

Supraparticles (SPs) are assemblies of colloidal particles whose properties can be tuned by modifying the chemistry, shape, and size of the colloidal particles as well as their arrangement in the SP. SPs with internal porosity are of particular interest for catalysis, photonics, and adsorption applications because of their high surface area and tunable pore size distribution. SPs are often fabricated by droplet drying, and the nonequilibrium nature of drying processes may provide an additional handle to control particle arrangement within the SP. Here, we use mesoscale particle-based simulations to explore the drying-induced assembly of SPs made from rod-shaped and spherical colloidal particles. We selectively remove one type of particle after drying and characterize the structure of the resulting porous SP. We find that the remaining particles form connected networks for most compositions, with rods percolating at lower volume fractions than spheres. Most of the resulting void volume forms a single contiguous space whose surface area closely follows the total surface area of the remaining component. The pore-size distribution, however, depends strongly on sphere size and on the removed component, reflecting differences in sphere-clustering and rod-bundling before removal. This work provides new insight into how particle size and shape, as well as processing conditions, might be used to manipulate porosity in SPs.

cond-mat.soft

Exploring the role of hydrodynamic interactions in spherically-confined drying colloidal suspensions

We study the distribution of colloidal particles confined in drying spherical droplets using both dynamic density functional theory (DDFT) and particle-based simulations. In particular, we focus on the advection-dominated regime typical of aqueous droplets drying at room temperature and systematically investigate the role of hydrodynamic interactions during this nonequilibrium process. In general, drying produces transient particle concentration gradients within the droplet in this regime, with a considerable accumulation of particles at the droplet's liquid-vapor interface. We find that these gradients become significantly larger with pairwise hydrodynamic interactions between colloidal particles instead of a free-draining hydrodynamic approximation; however, the solvent's boundary conditions at the droplet's interface (unbounded, slip, or no-slip) do not have a significant effect on the particle distribution. DDFT calculations leveraging radial symmetry of the drying droplet are in excellent agreement with particle-based simulations for free-draining hydrodynamics, but DDFT unexpectedly fails for pairwise hydrodynamic interactions after the particle concentration increases during drying, manifesting as an ejection of particles from the droplet. We hypothesize that this unphysical behavior originates from an inaccurate approximation of the two-body density correlations based on the bulk pair correlation function, which we support by measuring the confined equilibrium two-body density correlations using particle-based simulations. We identify some potential strategies for addressing this issue in DDFT.

cond-mat.soft