Solvent coarsening around colloids driven by temperature gradients

Using mesoscopic numerical simulations and analytical theory we investigate the coarsening of the solvent structure around a colloidal particle emerging after a temperature quench of the colloid surface. Qualitative differences in the coarsening mechanisms are found, depending on the composition of the binary liquid mixture forming the solvent and on the adsorption preferences of the colloid. For an adsorptionwise neutral colloid, as function of time the phase being next to its surface alternates. This behavior sets in on the scale of the relaxation time of the solvent and is absent for colloids with strong adsorption preferences. A Janus colloid, with a small temperature difference between its two hemispheres, reveals an asymmetric structure formation and surface enrichment around it, even if the solvent is within its one-phase region and if the temperature of the colloid is above the critical demixing temperature $T_c$ of the solvent. Our phenomenological model turns out to capture recent experimental findings according to which, upon laser illumination of a Janus colloid and due to the ensuing temperature gradient between its two hemispheres, the surrounding binary liquid mixture develops a concentration gradient.Comment: 8 pages, 4 figure

Phase diagram of a model for 3He-4He mixtures in three dimensions

A lattice model of 3He - 4He mixtures which takes into account the continuous rotational symmetry O(2) of the superfluid degrees of freedom of 4He is studied in the molecular-field approximation and by Monte Carlo simulations in three dimensions. In contrast to its two-dimensional version, for reasonable values of the interaction parameters the resulting phase diagram resembles that observed experimentally for 3He - 4He mixtures, for which phase separation occurs as a consequence of the superfluid transition. The corresponding continuum Ginzburg-Landau model with two order parameters describing 3He- 4He mixtures near tricriticality is derived from the considered lattice model. All coupling constants appearing in the continuum model are explicitly expressed in terms of the mean concentration of 4He, the temperature, and the microscopic interaction parameters characterizing the lattice system.Comment: 32 pages, 12 figures, submitted to the Phys. Rev.

Critical Casimir interactions around the consolute point of a binary solvent

Spatial confinement of a near-critical medium changes its fluctuation spectrum and modifies the corresponding order parameter distribution. These effects result in effective, so-called critical Casimir forces (CCFs) acting on the confining surfaces. These forces are attractive for like boundary conditions of the order parameter at the opposing surfaces of the confinement. For colloidal particles dissolved in a binary liquid mixture acting as a solvent close to its critical point of demixing, one thus expects the emergence of phase segregation into equilibrium colloidal liquid and gas phases. We analyze how such phenomena occur asymmetrically in the whole thermodynamic neighborhood of the consolute point of the binary solvent. By applying field-theoretical methods within mean-field approximation and the semi-empirical de Gennes-Fisher functional, we study the CCFs acting between planar parallel walls as well as between two spherical colloids and their dependence on temperature and on the composition of the near-critical binary mixture. We find that for compositions slightly poor in the molecules preferentially adsorbed at the surfaces, the CCFs are significantly stronger than at the critical composition, thus leading to pronounced colloidal segregation. The segregation phase diagram of the colloid solution following from the calculated effective pair potential between the colloids agrees surprisingly well with experiments and simulations

Current-mediated synchronization of a pair of beating non-identical flagella

The basic phenomenology of experimentally observed synchronization (i.e., a stochastic phase locking) of identical, beating flagella of a biflagellate alga is known to be captured well by a minimal model describing the dynamics of coupled, limit-cycle, noisy oscillators (known as the noisy Kuramoto model). As demonstrated experimentally, the amplitudes of the noise terms therein, which stem from fluctuations of the rotary motors, depend on the flagella length. Here we address the conceptually important question which kind of synchrony occurs if the two flagella have different lengths such that the noises acting on each of them have different amplitudes. On the basis of a minimal model, too, we show that a different kind of synchrony emerges, and here it is mediated by a current carrying, steady-state; it manifests itself via correlated "drifts" of phases. We quantify such a synchronization mechanism in terms of appropriate order parameters $Q$ and $Q_{\cal S}$ - for an ensemble of trajectories and for a single realization of noises of duration ${\cal S}$, respectively. Via numerical simulations we show that both approaches become identical for long observation times ${\cal S}$. This reveals an ergodic behavior and implies that a single-realization order parameter $Q_{\cal S}$ is suitable for experimental analysis for which ensemble averaging is not always possible.Comment: 10 pages, 2 figure

Sensitivity of the thermodynamics of two-dimensional systems towards the topological classes of their surfaces

Using Monte Carlo simulations we study the two-dimensional Ising model on triangular, square, and hexagonal lattices with various topologies. We focus on the behavior of the magnetic susceptibility and of the specific heat near the critical point of the planar bulk system. We find that scaling functions of these quantities on the spherical surface (Euler characteristic K = 2) differ from the scaling functions on the projective plane (K = 1) which, in turn, differ from the scaling functions on the torus and on the Klein bottle (both K = 0). This provides strong evidence that phase transitions of the Ising model on two-dimensional surfaces depend on their topologies.Comment: 25 pages, 10 figure

Correlations and forces in sheared fluids with or without quenching

Spatial correlations play an important role in characterizing material properties related to non-local effects. Inter alia, they can give rise to fluctuation-induced forces. Equilibrium correlations in fluids provide an extensively studied paradigmatic case, in which their range is typically bounded by the correlation length. Out of equilibrium, conservation laws have been found to extend correlations beyond this length, leading, instead, to algebraic decays. In this context, here we present a systematic study of the correlations and forces in fluids driven out of equilibrium simultaneously by quenching and shearing, both for non-conserved as well as for conserved Langevin-type dynamics. We identify which aspects of the correlations are due to shear, due to quenching, and due to simultaneously applying both, and how these properties depend on the correlation length of the system and its compressibility. Both shearing and quenching lead to long-ranged correlations, which, however, differ in their nature as well as in their prefactors, and which are mixed up by applying both perturbations. These correlations are employed to compute non-equilibrium fluctuation-induced forces in the presence of shear, with or without quenching, thereby generalizing the framework set out by Dean and Gopinathan. These forces can be stronger or weaker compared to their counterparts in unsheared systems. In general, they do not point along the axis connecting the centers of the small inclusions considered to be embedded in the fluctuating medium. Since quenches or shearing appear to be realizable in a variety of systems with conserved particle number, including active matter, we expect these findings to be relevant for experimental investigations.Comment: 19 pgs (15 main text + 4 appendices); 7 figure

Silicon on ceramic process. Silicon sheet growth development for the large-area silicon sheet task of the low-cost silicon solar array project

The technical and economic feasibility of producing solar-cell-quality sheet silicon was investigated. The sheets were made by coating one surface of carbonized ceramic substrates with a thin layer of large-grain polycrystalline silicon from the melt. Significant progress was made in all areas of the program

Dip-coating process: Silicon sheet growth development for the large-area silicon sheet task of the low-cost silicon solar array project

The objective of this research program is to investigate the technical and economic feasibility of producing solar-cell-quality sheet silicon by coating one surface of carbonized ceramic substrates with a thin layer of large-grain polycrystalline silicon from the melt. The past quarter demonstrated significant progress in several areas. Seeded growth of silicon-on-ceramic (SOC) with an EFG ribbon seed was demonstrated. Different types of mullite were successfully coated with silicon. A new method of deriving minority carrier diffusion length, L sub n from spectral response measurements was evaluated. ECOMOD cost projections were found to be in good agreement with the interim SAMIS method proposed by JPL. On the less positive side, there was a decrease in cell performance which we believe to be due to an unidentified source of impurities

Origin of attraction between likely charged hydrophobic and hydrophilic walls confining near-critical binary aquaeous mixture with ions

Effect of ionic solute on a near-critical binary aqueous mixture confined between charged walls with different adsorption preferences is considered within a simple density functional theory. For the near-critical system containing small amount of ions a Landau-type functional is derived based on the assumption that the correlation, $\xi$, and the Debye screening length, $\kappa^{-1}$, are both much larger than the molecular size. The corresponding approximate Euler-Lagrange equations aresolved analytically for ions insoluble in the organic solvent. Nontrivial concentration profile of the solvent is found near the charged hydrophobic wall as a result of the competition between the short-range attraction of the organic solvent and the electrostatic attraction of the hydrated ions. Excess of water may be present near the hydrophobic surface for some range of the surface charge and $\xi\kappa$. As a result, the effective potential between the hydrophilic and the hydrophobic surface can be repulsive far from the critical point, then attractive and again repulsive when the critical temperature is approached, in agreement with the recent experiment [Nellen at.al., Soft Matter {\bf 7}, 5360 (2011)]