We numerically investigate the adsorption of a variety of Janus particles (dumbbells, elongated dumbbells and spherocylinders) at a fluid–fluid interface by using a numerical method that takes into account the interfacial deformations. We also experimentally synthesize micrometer–sized charged Janus dumbbells and let them adsorb at a water–decane interface. We find a good agreement between numerical and experimental results.
We develop a phenomenological Landau-de Gennes (LdG) theory for lyotropic colloidal suspensions of bent rods using a Q-tensor expansion of the chemical-potential dependent grand potential. In addition, we introduce a bend flexoelectric term, coupling the polarization and the divergence of the Q-tensor, to study the stability of uniaxial (N), twist-bend (N TB ), and splay-bend (N SB ) nematic phases of colloidal bent rods. We first show that a mapping can be found between the LdG theory and the Oseen-Frank theory. By breaking the degeneracy between the splay and bend elastic constants, we find that the LdG theory predicts either an N-N TB -N SB or an N-N SB -N TB phase sequence upon increasing the particle concentration. Finally, we employ our theory to study the first-order N-N TB phase transition, for which we find that K 33 as well as its renormalized version K eff 33 remain positive at the transition, whereas K eff 33 vanishes at the nematic spinodal. We connect these findings to recent simulation results.
Inspired by recent experimental observations of spontaneous chain formation of cubic particles adsorbed at a fluid-fluid interface, we theoretically investigate whether capillary interactions can be responsible for this self-assembly process....
We show that an analogy between crowding in fluid and jammed phases of hard spheres captures the density dependence of the kissing number for a family of numerically generated jammed states. We extend this analogy to jams of mixtures of hard spheres in $d=3$ dimensions, and thus obtain an estimate of the random close packing (RCP) volume fraction, $\phi_{\textrm{RCP}}$, as a function of size polydispersity. We first consider mixtures of particle sizes with discrete distributions. For binary systems, we show agreement between our predictions and simulations, using both our own and results reported in previous works, as well as agreement with recent experiments from the literature. We then apply our approach to systems with continuous polydispersity, using three different particle size distributions, namely the log-normal, Gamma, and truncated power-law distributions. In all cases, we observe agreement between our theoretical findings and numerical results up to rather large polydispersities for all particle size distributions, when using as reference our own simulations and results from the literature. In particular, we find $\phi_{\textrm{RCP}}$ to increase monotonically with the relative standard deviation, $s_{\sigma}$, of the distribution, and to saturate at a value that always remains below 1.A perturbative expansion yields a closed-form expression for $\phi_{\textrm{RCP}}$ that quantitatively captures a distribution-independent regime for $s_{\sigma} < 0.5$. Beyond that regime, we show that the gradual loss in agreement is tied to the growth of the skewness of size distributions.
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