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Roland Roth

Publications and source records attributed to Roland Roth.

27 records · Page 2Linked to original sources

Modeling diffusion in colloidal suspensions by dynamical density functional theory using fundamental measure theory of hard spheres

We study the dynamics of colloidal suspensions of hard spheres that are subject to Brownian motion in the overdamped limit. We obtain the time evolution of the self and distinct parts of the van Hove function by means of dynamical density functional theory (DDFT). The free energy model for the hard sphere fluid that we use is the very accurate White Bear II version of Rosenfeld's fundamental measure theory. However, in order to remove interactions within the self part of the van Hove function a non-trivial modification has to be applied to the free energy functional. We compare our theoretical results with data that we obtain from dynamical Monte Carlo simulations and find that the latter are well described by our approach even for colloid packing fractions as large as 40%.

cond-mat.soft↗

Multivalent Ion-Activated Protein Adsorption Reflecting Bulk Reentrant Behavior

Protein adsorption at the solid-liquid interface is an important phenomenon that often can be observed as a first step in biological processes. Despite its inherent importance, still relatively little is known about the underlying microscopic mechanisms. Here, using multivalent ions, we demonstrate the control of the interactions and the corresponding adsorption of net-negatively charged proteins (bovine serum albumin) at a solid-liquid interface. This is demonstrated by ellipsometry and corroborated by neutron reflectivity and quartz-crystal microbalance experiments. We show that the reentrant condensation observed within the rich bulk phase behavior of the system featuring a nonmonotonic dependence of the second virial cofficient on salt concentration c_s is reflected in an intriguing way in the protein adsorption d(c_s) at the interface. Our findings are successfully described and understood by a model of ion-activated patchy interactions within the framework of classical density functional theory. In addition to the general challenge of connecting bulk and interface behavior, our work has implications for, inter alia, nucleation at interfaces.

physics.bio-ph↗

Parameterizing the surface free energy and excess adsorption of a hard-sphere fluid at a planar hard wall

he inhomogeneous structure of a fluid at a wall can be characterized in several ways. Within a thermodynamic description the surface free energy $γ$ and the excess adsorption $Γ$ are of central importance. For theoretical studies closed expression of $γ$ and $Γ$ can be very valuable; however, even for a well-studied model system such as a hard-sphere fluid at a planar hard wall, the accuracy of existing expressions for $γ$ and $Γ$, compared to precise computer simulation data, can still be improved. Here, we compare several known expressions for $γ$ and $Γ$ to the most precise computer simulation data. While good agreement is generally found at low to intermediate fluid densities, the existing parameterizations show significant deviation at high density. In this work, we propose new parameterizations for $γ$ and $Γ$ that agree with the simulation data within statistical error over the entire fluid density range.

cond-mat.stat-mech↗

Polyhedral colloidal `rocks': low-dimensional networks

We introduce a model system of anisotropic colloidal `rocks'. Due to their shape, the bonding introduced via non-absorbing polymers is profoundly different from spherical particles: bonds between rocks are rigid against rotation, leading to strong frustration. We develop a geometric model which captures the essence of the rocks. Experiments and simulations show that the colloid geometry leads to structures of low fractal dimension. This is in stark contrast to gels of spheres, whose rigidity results from locally dense regions. At high density the rocks form a quasi one-component glass.

cond-mat.soft↗

Depletion potentials in highly size-asymmetric binary hard-sphere mixtures: Comparison of accurate simulation results with theory

We report a detailed study, using state-of-the-art simulation and theoretical methods, of the depletion potential between a pair of big hard spheres immersed in a reservoir of much smaller hard spheres, the size disparity being measured by the ratio of diameters q=σ_s/σ_b. Small particles are treated grand canonically, their influence being parameterized in terms of their packing fraction in the reservoir, η_s^r. Two specialized Monte Carlo simulation schemes --the geometrical cluster algorithm, and staged particle insertion-- are deployed to obtain accurate depletion potentials for a number of combinations of q\leq 0.1 and η_s^r. After applying corrections for simulation finite-size effects, the depletion potentials are compared with the prediction of new density functional theory (DFT) calculations based on the insertion trick using the Rosenfeld functional and several subsequent modifications. While agreement between the DFT and simulation is generally good, significant discrepancies are evident at the largest reservoir packing fraction accessible to our simulation methods, namely η_s^r=0.35. These discrepancies are, however, small compared to those between simulation and the much poorer predictions of the Derjaguin approximation at this η_s^r. The recently proposed morphometric approximation performs better than Derjaguin but is somewhat poorer than DFT for the size ratios and small sphere packing fractions that we consider. The effective potentials from simulation, DFT and the morphometric approximation were used to compute the second virial coefficient B_2 as a function of η_s^r. Comparison of the results enables an assessment of the extent to which DFT can be expected to correctly predict the propensity towards fluid fluid phase separation in additive binary hard sphere mixtures with q\leq 0.1.

cond-mat.stat-mech↗

Selectivity in binary fluid mixtures: static and dynamical properties

Selectivity of particles in a region of space can be achieved by applying external potentials to influence the particles in that region. We investigate static and dynamical properties of size selectivity in binary fluid mixtures of two particles sizes. We find that by applying an external potential that is attractive to both kinds of particles, due to crowding effects, this can lead to one species of particles being expelled from that region, whilst the other species is attracted into the region where the potential is applied. This selectivity of one species of particle over the other in a localized region of space depends on the density and composition of the fluid mixture. Applying an external potential that repels both kinds of particles leads to selectivity of the opposite species of particles to the selectivity with attractive potentials. We use equilibrium and dynamical density functional theory to describe and understand the static and dynamical properties of this striking phenomenon. Selectivity by some ion-channels is believed to be due to this effect.

cond-mat.soft↗

Experimental observation of structural crossover in binary mixtures of colloidal hard spheres

Using confocal-microscopy we investigate the structure of binary mixtures of colloidal hard spheres with size ratio q=0.61. As a function of the packing fraction of the two particle species, we observe a marked change of the dominant wavelength in the pair correlation function. This behavior is in excellent agreement with a recently predicted structural crossover in such mixtures. In addition, the repercussions of structural crossover on the real-space structure of a binary fluid are analyzed. We suggest a relation between crossover and the lateral extension of networks containing only equally sized particles that are connected by nearest neighbor bonds. This is supported by Monte-Carlo simulations which are performed at different packing fractions and size ratios.

cond-mat.soft↗

Density functional theory for hard-sphere mixtures: the White-Bear version Mark II

In the spirit of the White-Bear version of fundamental measure theory we derive a new density functional for hard-sphere mixtures which is based on a recent mixture extension of the Carnahan-Starling equation of state. In addition to the capability to predict inhomogeneous density distributions very accurately, like the original White-Bear version, the new functional improves upon consistency with an exact scaled-particle theory relation in the case of the pure fluid. We examine consistency in detail within the context of morphological thermodynamics. Interestingly, for the pure fluid the degree of consistency of the new version is not only higher than for the original White-Bear version but also higher than for Rosenfeld's original fundamental measure theory.

cond-mat.soft↗

On the Physics of Size Selectivity

We demonstrate that two mechanisms used by biological ion channels to select particles by size are driven by entropy. With uncharged particles in an infinite cylinder, we show that a channel that attracts particles is small-particle selective and that a channel that repels water from the wall is large-particle selective. Comparing against extensive density-functional theory calculations of our model, we find that the main physics can be understood with surprisingly simple bulk models that neglect the confining geometry of the channel completely.

cond-mat.soft↗