arXiv subjects

S. Dietrich

Publications and source records attributed to S. Dietrich.

At least 73 records · Page 4Linked to original sources

arXiv2015

Implications of interface conventions for morphometric thermodynamics

Several model fluids in contact with planar, spherical, and cylindrical walls are investigated for small number densities within density functional theory. The dependence of the solid-fluid interfacial tension on the curvature of spherical and cylindrical walls is examined and compared with the corresponding expression derived within the framework of morphometric thermodynamics. Particular attention is paid to the implications of the choice of the interface location, which underlies the definition of the interfacial tension. We find that morphometric thermodynamics is never exact for the considered systems and that its quality as an approximation depends sensitively on the choice of the interface location.

cond-mat.stat-mech↗

arXiv2014

Phase diagram of fluid phases in ${}^3$He -${}^4$He mixtures

Fluid parts of the phase diagram of ${}^3$He -${}^4$He mixtures are obtained from a mean-field analysis of a suitable lattice gas model for binary liquid mixtures. The proposed model takes into account the continuous rotational symmetry O(2) of the superfluid degrees of freedom associated with ${}^4$He and includes the occurrence of vacancies. This latter degree of freedom allows the model to exhibit a vapor phase and hence can provide the theoretical framework to describe the experimental conditions for measurements of tricritical Casimir forces in ${}^3$He -${}^4$He wetting films.

cond-mat.stat-mech↗

arXiv2014

Enhanced wavelength-dependent surface tension of liquid-vapour interfaces

Due to the simultaneous presence of bulk-like and interfacial fluctuations the understanding of the structure of liquid-vapour interfaces poses a long-lasting and ongoing challenge for experiments, theory, and simulations. We provide a new analysis of this topic by combining high-quality simulation data for Lennard-Jones fluids with an unambiguous definition of the wavenumber-dependent surface tension $γ(q)$ based on the two-point correlation function of the fluid. Upon raising the temperature, $γ(q)$ develops a maximum at short wavelengths. We compare these results with predictions from density functional theory. Our analysis has repercussions for the interpretation of grazing-incidence small-angle X-ray scattering (GISAXS) at liquid interfaces.

cond-mat.stat-mech↗

arXiv2014

Structures of simple liquids in contact with nanosculptured surfaces

We present a density functional study of Lennard-Jones liquids in contact with a nano-corrugated wall. The corresponding substrate potential is taken to exhibit a repulsive hard core and a van der Waals attraction. The corrugation is modeled by a periodic array of square nano-pits. We have used the modified Rosenfeld density functional in order to study the interfacial structure of these liquids which with respect to their thermodynamic bulk state are considered to be deep inside their liquid phase. We find that already considerably below the packing fraction of bulk freezing of these liquids, inside the nanopits a three-dimensional-like density localization sets in. If the sizes of the pits are commensurate with the packing requirements, we observe high density spots separated from each other in all spatial directions by liquid of comparatively very low density. The number, shape, size, and density of these high density spots depend sensitively on the depth and width of the pits. Outside the pits, only layering is observed; above the pit openings these layers are distorted with the distortion reaching up to a few molecular diameters. We discuss quantitatively how this density localization is affected by the geometrical features of the pits and how it evolves upon increasing the bulk packing fraction. Our results are transferable to colloidal systems and pit dimensions corresponding to several diameters of the colloidal particles. For such systems the predicted unfolding of these structural changes can be studied experimentally on much larger length scales and more directly (e.g., optically) than for molecular fluids which typically call for sophisticated X-ray scattering.

cond-mat.stat-mech↗

arXiv2014

Critical Casimir forces between planar and crenellated surfaces

We study critical Casimir forces between planar walls and geometrically structured substrates within mean-field theory. As substrate structures, crenellated surfaces consisting of periodic arrays of rectangular crenels and merlons are considered. Within the widely used proximity force approximation, both the top surfaces of the merlons and the bottom surfaces of the crenels contribute to the critical Casimir force. However, for such systems the full, numerically determined critical Casimir forces deviate significantly fromthe pairwise addition formalismunderlying the proximity force approximation. A first-order correction to the proximity force approximation is presented in terms of a step contribution arising from the critical Casimir interaction between a planar substrate and the right-angled steps of the merlons consisting of their upper and lower edges as well as their sidewalls.

cond-mat.soft↗

arXiv2014

Alignment of cylindrical colloids near chemically patterned substrates induced by critical Casimir torques

Recent experiments have demonstrated a fluctuation-induced lateral trapping of spherical colloidal particles immersed in a binary liquid mixture near its critical demixing point and exposed to chemically patterned substrates. Inspired by these experiments, we study this kind of effective interaction, known as the critical Casimir effect, for elongated colloids of cylindrical shape. This adds orientational degrees of freedom. When the colloidal particles are close to a chemically structured substrate, a critical Casimir torque acting on the colloids emerges. We calculate this torque on the basis of the Derjaguin approximation. The range of validity of the latter is assessed via mean-field theory. This assessment shows that the Derjaguin approximation is reliable in experimentally relevant regimes, so that we extend it to Janus particles endowed with opposing adsorption preferences. Our analysis indicates that critical Casimir interactions are capable of achieving well-defined, reversible alignments both of chemically homogeneous and of Janus cylinders.

cond-mat.soft↗

arXiv2014

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.

cond-mat.soft↗

arXiv2014

Electrostatic interaction between colloidal particles trapped at an electrolyte interface

The electrostatic interaction between colloidal particles trapped at the interface between two immiscible electrolyte solutions is studied in the limit of small inter-particle distances. Within an appropriate model exact analytic expressions for the electrostatic potential as well as for the surface and line interaction energies are obtained. They demonstrate that the widely used superposition approximation, which is commonly applied to large distances between the colloidal particles, fails qualitatively at small distances and is quantitatively unreliable even at large distances. Our results contribute to an improved description of the interaction between colloidal particles trapped at fluid interfaces.

cond-mat.soft↗

arXiv2014

Order of wetting transitions in electrolyte solutions

For wetting films in dilute electrolyte solutions close to charged walls we present analytic expressions for their effective interface potentials. The analysis of these expressions renders the conditions under which corresponding wetting transitions can be first- or second-order. Within mean field theory we consider two models, one with short- and one with long-ranged solvent-solvent and solvent-wall interactions. The analytic results reveal in a transparent way that wetting transitions in electrolyte solutions, which occur far away from their critical point (i.e., the bulk correlation length is less than half of the Debye length) are always first-order if the solvent-solvent and solvent-wall interactions are short-ranged. In contrast, wetting transitions close to the bulk critical point of the solvent (i.e., the bulk correlation length is larger than the Debye length) exhibit the same wetting behavior as the pure, i.e., salt-free, solvent. If the salt-free solvent is governed by long-ranged solvent-solvent as well as long-ranged solvent-wall interactions and exhibits critical wetting, adding salt can cause the occurrence of an ion-induced first-order thin-thick transition which precedes the subsequent continuous wetting as for the salt-free solvent.

cond-mat.soft↗

arXiv2013

Capillary attraction induced collapse of colloidal monolayers at fluid interfaces

We investigate the evolution of a system of colloidal particles, trapped at a fluid interface and interacting via capillary attraction, as function of the range of the capillary interaction and temperature. We address the collapse of an initially homogeneous particle distribution and of a radially symmetric (disk--shaped) distribution of finite size, both theoretically by using a perturbative approach inspired by cosmological models and numerically by means of Brownian dynamics (BD) and dynamical density functional theory (DDFT). The results are summarized in a "dynamical phase diagram", describing a smooth crossover from collective (gravitational-like) collapse to local (spinodal-like) clustering. In this crossover region, the evolution exhibits a peculiar shock wave behavior at the outer rim of the contracting, disk-shaped distribution.

cond-mat.soft↗

arXiv2013

Critical Casimir forces between homogeneous and chemically striped surfaces

Recent experiments have measured the critical Casimir force acting on a colloid immersed in a binary liquid mixture near its continuous demixing phase transition and exposed to a chemically structured substrate. Motivated by these experiments, we study the critical behavior of a system, which belongs to the Ising universality class, for the film geometry with one planar wall chemically striped, such that there is a laterally alternating adsorption preference for the two species of the binary liquid mixture, which is implemented by surface fields. For the opposite wall we employ alternatively a homogeneous adsorption preference or homogeneous Dirichlet boundary conditions, which within a lattice model are realized by open boundary conditions. By means of mean-field theory, Monte Carlo simulations, and finite-size scaling analysis we determine the critical Casimir force acting on the two parallel walls and its corresponding universal scaling function. We show that in the limit of stripe widths small compared with the film thickness, on the striped surface the system effectively realizes Dirichlet boundary conditions, which generically do not hold for actual fluids. Moreover, the critical Casimir force is found to be attractive or repulsive, depending on the width of the stripes of the chemically patterned surface and on the boundary condition applied to the opposing surface.

cond-mat.stat-mech↗

arXiv2013

Critical Casimir Forces for Films with Bulk Ordering Fields

The confinement of long-ranged critical fluctuations in the vicinity of second-order phase transitions in fluids generates critical Casimir forces acting on confining surfaces or among particles immersed in a critical solvent. This is realized in binary liquid mixtures close to their consolute point $T_{c}$ which belong to the universality class of the Ising model. The deviation of the difference of the chemical potentials of the two species of the mixture from its value at criticality corresponds to the bulk magnetic filed of the Ising model. By using Monte Carlo simulations for this latter representative of the corresponding universality class we compute the critical Casimir force as a function of the bulk ordering field at the critical temperature $T=T_{c}$. We use a coupling parameter scheme for the computation of the underlying free energy differences and an energy-magnetization integration method for computing the bulk free energy density which is a necessary ingredient. By taking into account finite-size corrections, for various types of boundary conditions we determine the universal Casimir force scaling function as a function of the scaling variable associated with the bulk field. Our numerical data are compared with analytic results obtained from mean-field theory.

cond-mat.stat-mech↗

arXiv2013

Magnetization and susceptibility of polydisperse ferrofluids

On the basis of the mean spherical approximation of multicomponent dipolar hard sphere mixtures an analytical expression is proposed for the magnetic field dependence of the magnetization of size polydisperse ferrofluids. The polydispersity of the particle diameter is described by the gamma distribution function. Canonical ensemble Monte Carlo simulations have been performed in order to test these theoretical results for the initial susceptibility and the magnetization. The results for the magnetic properties of the polydisperse systems turn out to be in quantitative agreement with our present simulation data. In addition, we find good agreement between our theory and experimental data for magnetite-based ferrofluids.

cond-mat.soft↗

arXiv2013

Critical Casimir torques and forces acting on needles in two spatial dimensions

We investigate the universal orientation-dependent interactions between non-spherical colloidal particles immersed in a critical solvent by studying the instructive paradigm of a needle embedded in bounded two-dimensional Ising models at bulk criticality. For a needle in an Ising strip the interaction on mesoscopic scales depends on the width of the strip and the length, position, and orientation of the needle. By lattice Monte Carlo simulations we evaluate the free energy difference between needle configurations being parallel and perpendicular to the strip. We concentrate on small but nonetheless mesoscopic needle lengths for which analytic predictions are available for comparison. All combinations of boundary conditions for the needles and boundaries are considered which belong to either the "normal" or the "ordinary" surface universality class, i.e., which induce local order or disorder, respectively. We also derive exact results for needles of arbitrary mesoscopic length, in particular for needles embedded in a half plane and oriented perpendicular to the corresponding boundary as well as for needles embedded at the center line of a symmetric strip with parallel orientation.

cond-mat.soft↗

arXiv2013

Wetting in electrolyte solutions

Wetting of a charged substrate by an electrolyte solution is investigated by means of classical density functional theory applied to a lattice model. Within the present model the pure, i.e., salt-free solvent, for which all interactions are of the nearest-neighbor type only, exhibits a second-order wetting transition for all strengths of the substrate-particle and the particle-particle interactions for which the wetting transition temperature is nonzero. The influences of the substrate charge density and of the ionic strength on the wetting transition temperature and on the order of the wetting transition are studied. If the substrate is neutral, the addition of salt to the solvent changes neither the order nor the transition temperature of the wetting transition of the system. If the surface charge is nonzero, upon adding salt this continuous wetting transition changes to first-order within the wide range of substrate surface charge densities and ionic strengths studied here. As the substrate surface charge density is increased, at fixed ionic strength, the wetting transition temperature decreases and the prewetting line associated with the first-order wetting transition becomes longer. This decrease of the wetting transition temperature upon increasing the surface charge density becomes more pronounced by decreasing the ionic strength.

cond-mat.soft↗

arXiv2013

Stability of thin liquid films and sessile droplets under confinement

The stability of nonvolatile thin liquid films and of sessile droplets is strongly affected by finite size effects. We analyze their stability within the framework of density functional theory using the sharp kink approximation, i.e., on the basis of an effective interface Hamiltonian. We show that finite size effects suppress spinodal dewetting of films because it is driven by a long-wavelength instability. Therefore nonvolatile films are stable if the substrate area is too small. Similarly, nonvolatile droplets connected to a wetting film become unstable if the substrate area is too large. This instability of a nonvolatile sessile droplet turns out to be equivalent to the instability of a volatile drop which can attain chemical equilibrium with its vapor.

cond-mat.soft↗

arXiv2013

Many-body effects for critical Casimir forces

Within mean-field theory we calculate the scaling functions associated with critical Casimir forces for a system consisting of two spherical colloids immersed in a binary liquid mixture near its consolute point and facing a planar, homogeneous substrate. For several geometrical arrangements and boundary conditions we analyze the normal and the lateral critical Casimir forces acting on one of the two colloids. We find interesting features such as a change of sign of these forces upon varying either the position of one of the colloids or the temperature. By subtracting the pairwise forces from the total force we are able to determine the many-body forces acting on one of the colloids. We have found that the many-body contribution to the total critical Casimir force is more pronounced for small colloid-colloid and colloid-substrate distances, as well as for temperatures close to criticality, where the many-body contribution to the total force can reach up to 25%.

cond-mat.soft↗

arXiv2012

Local theory for ions in binary liquid mixtures

The influence of ions on the bulk phase behavior of binary liquid mixtures acting as their solvents and on the corresponding interfacial structures close to a planar wall is investigated by means of density functional theory based on local descriptions of the effective interactions between ions and their solvents. The bilinear coupling approximation (BCA), which has been used in numerous previous related investigations, is compared with a novel local density approximation (LDA) for the ion-solvent interactions. It turns out that within BCA the bulk phase diagrams, the two-point correlation functions, and critical adsorption exhibit qualitative features which are not compatible with the available experimental data. These discrepancies do not occur within the proposed LDA. Further experimental investigations are suggested which assess the reliability of the proposed LDA. This approach allows one to obtain a consistent and rather general understanding of the effects of ions on solvent properties. From our analysis we infer in particular that there can be an experimentally detectable influence of ions on binary liquid mixtures due to steric effects but not due to charge effects.

cond-mat.soft↗