arXiv subjects

S. Dietrich

Publications and source records attributed to S. Dietrich.

At least 19 recordsLinked to original sources

arXiv2024

Critical Casimir levitation of colloids above a bull's-eye pattern

Critical Casimir forces emerge among particles or surfaces immersed in a near-critical fluid, with the sign of the force determined by surface properties and with its strength tunable by minute temperature changes. Here, we show how such forces can be used to trap a colloidal particle and levitate it above a substrate with a bull's-eye pattern consisting of a ring with surface properties opposite to the rest of the substrate. Using the Derjaguin approximation and mean-field calculations, we find a rich behavior of spherical colloids at such a patterned surface, including sedimentation towards the ring and levitation above the ring (ring levitation) or above the bull's-eye's center (point levitation). Within the Derjaguin approximation, we calculate a levitation diagram for point levitation showing the depth of the trapping potential and the height at which the colloid levitates, both depending on the pattern properties, the colloid size, and the solution temperature. Our calculations reveal that the parameter space associated with point levitation shrinks if the system is driven away from a critical point, while, surprisingly, the trapping force becomes stronger. We discuss the application of critical Casimir levitation for sorting colloids by size and for determining the thermodynamic distance to criticality. Our results show that critical Casimir forces provide rich opportunities for controlling the behavior of colloidal particles at patterned surfaces.

cond-mat.soft↗

arXiv2024

Nanoalignment by Critical Casimir Torques

The manipulation of microscopic objects requires precise and controllable forces and torques. Recent advances have led to the use of critical Casimir forces as a powerful tool, which can be finely tuned through the temperature of the environment and the chemical properties of the involved objects. For example, these forces have been used to self-organize ensembles of particles and to counteract stiction caused by Casimir-Liftshitz forces. However, until now, the potential of critical Casimir torques has been largely unexplored. Here, we demonstrate that critical Casimir torques can efficiently control the alignment of microscopic objects on nanopatterned substrates. We show experimentally and corroborate with theoretical calculations and Monte Carlo simulations that circular patterns on a substrate can stabilize the position and orientation of microscopic disks. By making the patterns elliptical, such microdisks can be subject to a torque which flips them upright while simultaneously allowing for more accurate control of the microdisk position. More complex patterns can selectively trap 2D-chiral particles and generate particle motion similar to non-equilibrium Brownian ratchets. These findings provide new opportunities for nanotechnological applications requiring precise positioning and orientation of microscopic objects.

cond-mat.soft↗

arXiv2023

Critical Casimir forces in soft matter

We review recent advances in the theoretical, numerical, and experimental studies of critical Casimir forces in soft matter, with particular emphasis on their relevance for the structures of colloidal suspensions and on their dynamics. Distinct from other interactions which act in soft matter, such as electrostatic and van der Waals forces, critical Casimir forces are effective interactions characterised by the possibility to control reversibly their strength via minute temperature changes, while their attractive or repulsive character is conveniently determined via surface treatments or by structuring the involved surfaces. These features make critical Casimir forces excellent candidates for controlling the equilibrium and dynamical properties of individual colloids or colloidal dispersions as well as for possible applications in micro-mechanical systems. In the past 25 years a number of theoretical and experimental studies have been devoted to investigate these forces primarily under thermal equilibrium conditions, while their dynamical and non-equilibrium behaviour is a largely unexplored subject open for future investigations.

cond-mat.soft↗

arXiv2022

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.

cond-mat.stat-mech↗

arXiv2022

Critical Casimir Effect: Exact Results

In any medium there are fluctuations due to temperature or due to the quantum nature of its constituents. If a material body is immersed into such a medium, its shape and the properties of its constituents modify the properties of the surrounding medium and its fluctuations. If in the same medium there is a second body then -- in addition to all direct interactions between them -- the modifications due to the first body influence the modifications due to the second body. This mutual influence results in a force between these bodies. If the excitations of the medium, which mediate the effective interaction between the bodies, are massless, this force is long-ranged and nowadays known as a Casimir force. If the fluctuating medium consists of the confined electromagnetic field in vacuum, one speaks of the quantum mechanical Casimir effect. In the case that the order parameter of material fields fluctuates - such as differences of number densities or concentrations - and that the corresponding fluctuations of the order parameter are long-ranged, one speaks of the critical Casimir effect. This holds, e.g., in the case of systems which undergo a second-order phase transition and which are thermodynamically located near the corresponding critical point, or for systems with a continuous symmetry exhibiting Goldstone mode excitations. Here we review the currently available exact results concerning the critical Casimir effect in systems encompassing the one-dimensional Ising, XY, and Heisenberg models, the two-dimensional Ising model, the Gaussian and the spherical models, as well as the mean field results for the Ising and the XY model. Special attention is paid to the influence of the boundary conditions on the behavior of the Casimir force.

cond-mat.stat-mech↗

arXiv2022

Pumping and mixing in active pores

We show both numerically and analytically that a chemically patterned active pore can act as a micro/nano-pump for fluids, even if it is fore-aft symmetric. This is possible due to a spontaneous symmetry breaking which occurs when advection rather than diffusion is the dominant mechanism of solute transport. We further demonstrate that, for pumping and tuning the flow rate, a combination of geometrical and chemical inhomogeneities is required. For certain parameter values, the flow is unsteady, and persistent oscillations with a tunable frequency appear. Finally, we find that the flow may lose its axial symmetry and hence promotes mixing in the low Reynolds number regime.

cond-mat.soft↗

arXiv2022

Structure of electrolyte solutions at non-uniformly charged surfaces on a variety of length scales

The structures of dilute electrolyte solutions close to non-uniformly charged planar substrates are systematically studied within the entire spectrum of microscopic to macroscopic length scales by means of a unified classical density functional theory (DFT) approach. This is in contrast to previous investigations, which are applicable either to short or to long length scales. It turns out that interactions with microscopic ranges, e.g., due to the hard cores of the fluid molecules and ions, have negligible influence on the formation of non-uniform lateral structures of the electrolyte solutions. This partly justifies the Debye-Hückel approximation schemes applied in previous studies of that system. In general, a coupling between the lateral and the normal fluid structures leads to the phenomenology that, upon increasing the distance from the substrate, less details of the lateral non-uniformities contribute to the fluid structure, such that ultimately only large-scale surface features remain relevant. It can be expected that this picture also applies to other fluids characterized by several length scales.

cond-mat.soft↗

arXiv2021

Intrusion of liquids into liquid infused surfaces with nanoscale roughness

We present a theoretical study of the intrusion of an ambient liquid into pores of a nano-corrugated wall w. The pores are prefilled with a liquid lubricant which adheres to the walls of the pores more strongly than the ambient liquid. The two liquids are modeled as a binary mixture of two types of particles, A and B. The mixture can decompose into an A-rich(ambient) liquid, and a B-rich(lubricant) liquid. The wall attracts B particles more strongly than A particles. The ratio of w-A to w-B interaction strengths is changed to tune the contact angle $θ_{AB}$ formed by the A-rich/B-rich liquid interface between the two fluids and the corresponding planar wall. We use classical density functional theory, in order to capture the effects of microscopic details on the intrusion transition as a function of composition and pressure of the ambient liquid, for various values of $θ_{AB}$ and different pit sizes. We also studied the reverse process in which a pore initially filled with the ambient liquid is refilled with the lubricant. For small $θ_{AB}$ ,there is no hysteresis. However, beyond a certain $θ_{AB}$, we find the presence of hysteresis, which increases with increasing $θ_{AB}$. The dependence of location of the intrusion on $θ_{AB}$ and on the pit size, qualitatively follows the corresponding shift of the capillary-coexistence line away from the bulk liquid-liquid coexistence line, as predicted by a macroscopic capillarity model. The quantitative discrepancies become larger for narrower cavities. For the considered geometry, macroscopic capillarity theory predicts an open hysteresis loop above a threshold value of $θ_{AB} = 54.7^\circ$. This threshold, however, shifts to much higher values if widths of the pores become smaller than roughly ten times the diameter of the fluid particles.

cond-mat.soft↗

arXiv2021

Fluctuations of the critical Casimir force

The critical Casimir force (CCF) arises from confining fluctuations in a critical fluid and thus it is a fluctuating quantity itself. While the mean CCF is universal, its (static) variance has previously been found to depend on the microscopic details of the system which effectively set a large-momentum cutoff in the underlying field theory, rendering it potentially large. This raises the question how the properties of the force variance are reflected in experimentally observable quantities, such as the thickness of a wetting film or the position of a suspended colloidal particle. Here, based on a rigorous definition of the instantaneous force, we analyze static and dynamic correlations of the CCF for a conserved fluid in film geometry for various boundary conditions within the Gaussian approximation. We find that the dynamic correlation function of the CCF is independent of the momentum cutoff and decays algebraically in time. Within the Gaussian approximation, the associated exponent depends only on the dynamic universality class but not on the boundary conditions. We furthermore consider a fluid film, the thickness of which can fluctuate under the influence of the time-dependent CCF. The latter gives rise to an effective non-Markovian noise in the equation of motion of the film boundary and induces a distinct contribution to the position variance. Within the approximations used here, at short times, this contribution grows algebraically in time whereas, at long times, it saturates and contributes to the steady-state variance of the film thickness.

cond-mat.stat-mech↗

arXiv2020

Wetting behavior of a colloidal particle trapped at a composite liquid-vapor interface of a binary liquid mixture

A partially miscible binary liquid mixture, composed of A and B particles, is considered theoretically under conditions for which a stable A-rich liquid phase is in thermal equilibrium with the vapor phase. The B-rich liquid is metastable. The liquids and the thermodynamic conditions are chosen such, that the interface between the A-rich liquid and the vapor contains an intervening wetting film of the B-rich phase. In order to obtain information about the large-scale fluid structure around a colloidal particle, which is trapped at such a composite liquid-vapor interface, three related and linked wetting phenomena at planar liquid-vapor, wall-liquid, and wall-vapor interfaces are studied analytically, using classical density functional theory in conjunction with the sharp-kink approximation for the number density profiles of the A and B particles. If in accordance with the so-called mixing rule the strength of the A-B interaction is given by the geometric mean of the strengths of the A-A and B-B interactions, and similarly the ratio between the wall-A and the wall-B interaction, the scenario, in which the colloid is enclosed by a film of the B-rich liquid, can be excluded. Up to six distinct wetting scenarios are possible, if the above mixing rules for the fluid-wall and for the fluid-fluid interactions are relaxed. The way the space of system parameters is divided into domains corresponding to the six scenarios, and which of the domains actually appear, depends on the signs of the deviations from the mixing rule prescriptions. Relevant domains emerge, if the ratio between the strengths of the wall-A and the wall-B interactions is reduced as compared to the mixing rule prescription, or if the strength of the A-B interaction is increased to values above the one from the mixing rule prescription. The range, within which the contact angle may vary inside the various domains, is also studied.

cond-mat.soft↗

arXiv2020

Self-motility of an active particle induced by correlations in the surrounding solution

Current models of phoretic transport rely on molecular forces creating a "diffuse" particle-fluid interface. We investigate theoretically an alternative mechanism, in which a diffuse interface emerges solely due to a non-vanishing correlation length of the surrounding solution. This mechanism can drive self-motility of a chemically active particle. Numerical estimates indicate that the velocity can reach micrometers per second. The predicted phenomenology includes a bilinear dependence of the velocity on the activity and a possible double velocity reversal upon varying the correlation length.

cond-mat.soft↗

arXiv2020

The role of counterions in ionic liquid crystals

Previous theoretical studies of calamitic (i.e., rod-like) ionic liquid crystals (ILCs) based on an effective one-species model led to indications of a novel smectic-A phase with a layer spacing being much larger than the length of the mesogenic (i.e., liquid-crystal forming) ions. In order to rule out the possibility that this wide smectic-A phase is merely an artifact caused by the one-species approximation, we investigate an extension which accounts explicitly for cations and anions in ILCs. Our present findings, obtained by grand canonical Monte Carlo simulations, show that the phase transitions between the isotropic and the smectic-A phases of the cation-anion system are in qualitative agreement with the effective one-species model used in the preceding studies. In particular, for ILCs with mesogenes (i.e., liquid-crystal forming species) carrying charged sites at their tips, the wide smectic-A phase forms, at low temperatures and within an intermediate density range, in between the isotropic and a hexagonal crystal phase. We find that in the ordinary smectic-A phase the spatial distribution of the counterions of the mesogens is approximately uniform, whereas in the wide smectic-A phase the small counterions accumulate in between the smectic layers. Due to this phenomenology the wide smectic-A phase could be interesting for applications which hinge on the presence of conductivity channels for mobile ions.

cond-mat.soft↗

arXiv2020

Heterogeneous surface charge confining an electrolyte solution

The structure of dilute electrolyte solutions close to a surface carrying a spatially inhomogeneous surface charge distribution is investigated by means of classical density functional theory (DFT) within the approach of fundamental measure theory (FMT). For electrolyte solutions the influence of these inhomogeneities is particularly strong because the corresponding characteristic length scale is the Debye length, which is large compared to molecular sizes. Here a fully three-dimensional investigation is performed, which accounts explicitly for the solvent particles, and thus provides insight into effects caused by ion-solvent coupling. The present study introduces a versatile framework to analyze a broad range of types of surface charge heterogeneities even beyond the linear response regime. This reveals a sensitive dependence of the number density profiles of the fluid components and of the electrostatic potential on the magnitude of the charge as well as on details of the surface charge patterns at small scales.

cond-mat.soft↗

arXiv2020

Transient coarsening and the motility of optically heated Janus colloids in a binary liquid mixture

A gold-capped Janus particle suspended in a near-critical binary liquid mixture can self-propel under illumination. We have immobilized such a particle in a narrow channel and studied the nonequilibrium dynamics of a binary solvent around it, using experiment and numerical simulations. For the latter we consider both a purely diffusive and a hydrodynamic model. All approaches indicate that the early time dynamics is purely diffusive and characterized by composition layers traveling with a constant speed from the surface of the colloid into the bulk. Subsequently, hydrodynamic effects set in and the transient state is destroyed by strong nonequilibrium concentration fluctuations, which arise as a result of the temperature gradient and the vicinity of the critical point of the binary liquid mixture. They give rise to a complex, permanently changing coarsening patterns. For a mobile particle, the transient dynamics results in propulsion in the direction opposite to that observed after the steady state is attained.

cond-mat.soft↗

arXiv2020

Bridging transitions and capillary forces for colloids in a slit

Capillary bridges can form between colloids immersed in a two phase fluid, e.g., in a binary liquid mixture, if the surface of the colloids prefers the species other than the one favored in the bulk liquid. Here, we study the formation of liquid bridges induced by confining colloids to a slit, with the slit walls having a preference opposite to the one of the colloid surface. Using mean field theory, we show that there is a line of first-order phase transitions between the bridge and the no-bridge states, which ends at a critical point. By decreasing the slit width, this critical point is shifted towards smaller separations between the colloids. However, at very small separations, and far from criticality, we observe only a minor influence of the slit width on the location of the transition. Monte Carlo simulations of the Ising model, which mimics incompressible binary liquid mixtures, confirm the occurrence of the bridging transitions, as manifested by the appearance of bistable regions where both the bridge and the no-bridge configurations are (meta)stable. Interestingly, we find no bistability in the case of small colloids, but we observe a sharpening of the transition when the colloid size increases. In addition, we demonstrate that the capillary force acting between the colloids can depend sensitively on the slit width, and varies drastically with temperature, thus achieving strengths orders of magnitude higher than at criticality of the fluid.

cond-mat.soft↗

arXiv2019

Numerical simulations of self-diffusiophoretic colloids at fluid interfaces

The dynamics of active colloids is very sensitive to the presence of boundaries and interfaces which therefore can be used to control their motion. Here we analyze the dynamics of active colloids adsorbed at a fluid-fluid interface. By using a mesoscopic numerical approach which relies on an approximated numerical solution of the Navier-Stokes equation, we show that when adsorbed at a fluid interface, an active colloid experiences a net torque even in the absence of a viscosity contrast between the two adjacent fluids. In particular, we study the dependence of this torque on the contact angle of the colloid with the fluid-fluid interface and on its surface properties. We rationalize our results via an approximate approach which accounts for the appearance of a local friction coefficient. By providing insight into the dynamics of active colloids adsorbed at fluid interfaces, our results are relevant for two-dimensional self assembly and emulsion stabilization by means of active colloids.

cond-mat.soft↗

arXiv2019

Wetting of soft substrates

Within mean-field theory we study wetting of elastic substrates. Our analysis is based on a grand canonical free energy functional of the fluid number density and of the substrate displacement field. The substrate is described in terms of the linear theory of elasticity, parametrized by two Lamé coefficients. The fluid contribution is of the van der Waals type. Two potentials characterize the interparticle interactions in the system. The long-ranged attraction between the fluid particles is described by a potential $w(r)$, and $v(r)$ characterizes the substrate-fluid interaction. By integrating out the elastic degrees of freedom we obtain an effective theory for the fluid number density alone. Its structure is similar to the one for wetting of an inert substrate. However, the potential $w(r)$ is replaced by an effective potential which, in addition to $w(r)$, contains a term bilinear in $v(r)$. We discuss the corresponding wetting transitions in terms of an effective interface potential $ω(\ell)$, where $\ell$ denotes the thickness of the wetting layer. We show that in the case of algebraically decaying interactions the elasticity of the substrate may suppress critical wetting transitions, and may even turn them first order.

cond-mat.soft↗

arXiv2019

Cassie-Wenzel transition of a binary liquid mixture on a nano-sculptured surface

The Cassie-Wenzel transition of a symmetric binary liquid mixture in contact with a nano-corrugated wall is studied. The corrugation consists of a periodic array of nano-pits with square cross sections. The substrate potential is the sum over Lennard-Jones interactions, describing the pairwise interaction between the wall particles $C$ and the fluid particles. The liquid is composed of two species of particles, $A$ and $B$, which have the same size and equal $A - A$ and $B - B$ interactions. The liquid particles interact between each other also via $A - B$ Lennard-Jones potentials. We have employed classical density functional theory to determine the equilibrium structure of binary liquid mixtures in contact with the nano-corrugated surface. Liquid intrusion into the pits is studied as a function of various system parameters such as the composition of the liquid, the strengths of various inter-particle interactions, as well as the geometric parameters of the pits. The binary liquid mixture is taken to be at its mixed-liquid-vapor coexistence. For various sets of parameters the results obtained for the Cassie - Wenzel transition, as well as for the metastability of the two corresponding thermodynamic states, are compared with macroscopic predictions in order to check the range of validity of the macroscopic theories for systems exposed to nanoscopic confinements. Distinct from the macroscopic theory, it is found that the Cassie - Wenzel transition cannot be predicted based on the knowledge of a single parameter, such as the contact angle within the macroscopic theory.

physics.comp-ph↗