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A. L. Kolesnikov

Publications and source records attributed to A. L. Kolesnikov.

At least 19 recordsLinked to original sources

Modified Poisson-Boltzmann equations and macroscopic forces in inhomogeneous ionic fluids

We propose a field-theoretical approach based on the thermodynamic perturbation theory and within it derive a grand thermodynamic potential of the inhomogeneous ionic fluid as a functional of electrostatic potential for an arbitrary reference fluid system. We obtain a modified Poisson-Boltzmann equation as the Euler-Lagrange equation for the obtained functional. Applying Noether's theorem to this functional, we derive a general mean-field expression for the stress tensor consistent with the respective modified Poisson-Boltzmann equation. We derive a general expression for the macroscopic force acting on the dielectric or conductive body immersed in an ionic fluid. In particular, we derive a general mean-field expression for the disjoining pressure of an ionic fluid in a slit pore. We apply the developed formalism to describe three ionic fluid models of practical importance: nonpolarizable models (including the well-known Poisson-Boltzmann and Poisson-Fermi equations), polarizable models (ions carry nonzero permanent dipole or static polarizability), and models of ion-dipole mixtures (including the well-known Poisson-Boltzmann-Langevin equation). For these models, we obtain modified Poisson-Boltzmann equations and respective stress tensors, which could be valuable for different applications, where it is necessary to estimate the macroscopic forces acting on the dielectric or conductive bodies (electrodes, colloids, membranes, {\it etc}.) together with the local electrostatic potential (field) and ionic concentrations.

cond-mat.soft↗

Electrosorption-induced deformation of a porous electrode with non-convex pore geometry in electrolyte solutions: a theoretical study

Porous carbon is well known as a good candidate for the development of electrochemical double-layer capacitors. Predominantly, many conventional carbons are microporous and often well described by the assumption of slit pore geometry. However, there is a class of carbons that is significantly different from the others, namely templated mesoporous carbons. In this work, we study electrosorption-induced deformation in CMK-3-like mesopores having nonconvex geometry applying a mean-field approach. The model is based on the modified Poisson-Boltzmann equation taking into account the excluded volume of the ions within the hard-sphere model in the Percus-Yevick approximation. We assume that the deformation is caused by two effects: ion osmotic pressure and electrostatic interactions of the electric double layers on charged rods. The latter were calculated via the Maxwell stress tensor agreeing with the modified Poisson-Boltzmann equation. We estimated the pore-load modulus of the CMK-3-like material and found an agreement with the previously obtained values by small-angle neutron scattering (SANS). Additionally, we studied the differential capacitance in the non-convex pore geometry and found that the behavior of the differential capacitance profiles was similar to that of the profiles obtained for flat electric double layers. Namely, we obtained the crowding regime at rather high voltages and more pronounced profile asymmetry with increasing differences in the ionic sizes.

cond-mat.soft↗

Theory of ionic liquids with polarizable ions on a charged electrode

We formulate a general mean-field theory of a flat electric double layer in ionic liquids and electrolyte solutions with ions possessing static polarizability and a permanent dipole moment on a charged electrode. We establish a new analytical expression for electric double layer differential capacitance determining it as an absolute value of the ratio of the local ionic charge density to the local electric field on an electrode surface. We demonstrate that this expression generalizes the analytical expressions previously reported by Kornyshev and Maggs and Podgornik. Using the obtained analytical expression, we explore new features of the differential capacitance behavior with an increase in the static polarizability and permanent dipole moment of cations. We relate these features to the behavior of ionic concentrations on the electrode. In particular, we elucidate the role of the competition between the dielectrophoretic attraction and Coulomb repulsion forces acting on polarizable or polar cations in the electric double layer in the behavior of the differential capacitance. The developed theoretical model and obtained theoretical findings could be relevant for different electrochemical applications, e.g. batteries, supercapacitors, catalysis, electrodeposition, etc.

cond-mat.stat-mech↗

Computation of drug solvation free energy in supercritical CO2: alternatives to all-atom computer simulations

Despite the modern level of development of computational chemistry methods and techno-logical progress, fast and accurate determination of solvation free energy remains a huge problem for physical chemists. In this paper, we describe two computational schemes that can potentially solve this problem. We consider systems of poorly soluble drug compounds in supercritical carbon dioxide. Considering that the biggest contribution among all inter-molecular interactions is made by van der Waals interactions, we model solute and solvent particles as coarse-grained ones interacting via the effective Lennard-Jones potential. The first proposed approach is based on the classical density functional theory and the second one relies on molecular dynamics simulation of the Lennard-Jones fluid. Sacrificing the precision of the molecular structure description while capturing the phase behavior of the fluid with sufficient accuracy, we propose computationally advantageous paths to obtaining the solvation free energy values with the accuracy satisfactory for engineering applications. The agreement reached between the results of such coarse-graining models and the experimental data indicates that the use of the all-atom molecular dynamic simulations for the studied systems seems to be excessive.

physics.chem-ph↗

On gyration radius distributions of star-like macromolecules

Using the path integral approach, we obtain the characteristic functions of the gyration radius distributions for Gaussian star and Gaussian rosette macromolecules. We derive the analytical expressions for cumulants of the both distributions. Applying the steepest descent method, we estimate the probability distribution functions of the gyration radius in the limit of a large number of star and rosette arms in two limiting regimes: for strongly expanded and strongly collapsed macromolecules. We show that in both cases, in the regime of a large gyration radius relative to its mean-square value, the probability distribution functions can be described by the Gaussian functions. In the shrunk macromolecule regime, both distribution functions tend to zero faster than any power of the gyration radius. Based on the asymptotic behavior of the distribution functions and the behavior of statistical dispersions, we demonstrate that the probability distribution function for the rosette is more densely localized near its maximum than that for the star polymer. We construct the interpolation formula for the gyration radius distribution for the Gaussian star macromolecule which can help to take into account the conformational entropy of the flexible star macromolecules within the Flory-type mean-field theories

cond-mat.soft↗

A crossover of the solid substances solubility in supercritical fluids: what is it in fact?

We investigate a well-known phenomenon of the appearance of the crossover points, corresponding to the intersections of the solubility isotherms of the solid compound in supercritical fluid. Opposed to the accepted understanding of the existence of two fixed crossover points, which confine the region of the inverse isobaric temperature dependence of the solubility, we have found that these points tend to shift with the change of the temperature and in the limit of the certain threshold value they converge to a single point. We demonstrate this analyzing the solubility data of a set of poorly soluble drug compounds, which have been computed in a wide area of the phase diagram via the approach, based on the classical density functional theory. Thorough analysis of the available in the literature experimental solubility data is found to be in an agreement with our conclusions, as one can find that the wider temperature region of the experimental study is, the more pronounced effect of the crossover points drift can be observed.

cond-mat.soft↗

Two-component electrolyte solutions with dipolar cations on a charged electrode: Theory and computer simulations

The development of advanced electrochemical devices for energy conversion and storage requires fine tuning of electrode reactions, which can be accomplished by altering the electrode/solution interface structure. Particularly, in case of an alkali-salt electrolyte the electric double layer (EDL) composition can be managed by introducing organic cations (e.g. room temperature ionic liquid cations) that may possess polar fragments. To explore this approach, we develop a theoretical model predicting the efficient replacement of simple (alkali) cations with dipolar (organic) ones within the EDL. For the typical values of the molecular dipole moment ($2-4~D$) the effect manifests itself at the surface charge densities higher than 30 $μC/cm^2$. We show that the predicted behavior of the system is in qualitative agreement with the molecular dynamics simulation results.

cond-mat.soft↗

Nonlocal density functional theory of water taking into account many-body dipole correlations: Binodal and surface tension of 'liquid-vapour' interface

In this paper we formulate a nonlocal density functional theory of inhomogeneous water. We model a water molecule as a couple of oppositely charged sites. The negatively charged sites interact with each other through the Lennard-Jones potential (steric and dispersion interactions), square-well potential (short-range specific interactions due to electron charge transfer), and Coulomb potential, whereas the positively charged sites interact with all types of sites by applying the Coulomb potential only. Taking into account the nonlocal packing effects via the fundamental measure theory (FMT), dispersion and specific interactions in the mean-field approximation, and electrostatic interactions at the many-body level through the random phase approximation, we describe the liquid-vapour interface. We demonstrate that our model without explicit account of the association of water molecules due to hydrogen bonding and with explicit account of the many-body electrostatic interactions at the many-body level is able to describe the liquid-vapour coexistence curve and the surface tension at the ambient pressures and temperatures. We obtain very good agreement with available in the literature MD simulation results for density profile of liquid-vapour interface at ambient state parameters. The formulated theory can be used as a theoretical background for describing of the capillary phenomena, occurring in micro- and mesoporous materials.

cond-mat.soft↗

Carbamazepine solubility in supercritical CO$_2$: a comprehensive study

In this paper we present our study of carbamazepine solubility in supercritical carbon dioxide. We have calculated the solubility values along two isochores corresponding to the CO$_2$ densities $ρ= 1.1ρ_{cr}(CO_2)$ and $ρ= 1.3ρ_{cr}(CO_2)$, where $ρ_{cr}(CO_2)$ is the critical density of CO$_2$, in the temperature range from $313$ to $383~K$, as well as along three isotherms at $T=318$, $328$ and $348~K$ by an approach based on the classical density functional theory. The solubility values were also obtained using in situ IR spectroscopy and molecular dynamics simulations along the mentioned isochores and isotherms, respectively. Because the density functional theory only takes into account the Lennard-Jones interactions, it can be expected to underestimate the solubility values when compared to the experimental ones. However, we have shown that the data calculated within the classical density functional theory qualitatively reproduce the solubility trends obtained by IR spectroscopy and molecular dynamics simulation. Moreover, the obtained position of the upper crossover pressure is in good agreement with the experimental literature results.

cond-mat.mtrl-sci↗

Statistical description of co-nonsolvency suppression at high pressures

We present an application of Flory-type self-consistent field theory of the flexible polymer chain dissolved in the binary mixture of solvents to theoretical description of co-nonsolvency. We show that our theoretical predictions are in good quantitative agreement with the recently published MD simulation results for the conformational behavior of a Lennard-Jones flexible chain in a binary mixture of the Lennard-Jones fluids. We show that our theory is able to describe co-nonsolvency suppression through pressure enhancement to extremely high values recently discovered in experiment and reproduced by full atomistic MD simulations. Analysing a co-solvent concentration in internal polymer volume at different pressure values, we speculate that this phenomenon is caused by the suppression of the co-solvent preferential solvation of the polymer backbone at rather high pressure imposed. We show that when the co-solvent-induced coil-globule transition takes place, the entropy and the enthalpy contributions to the solvation free energy abruptly decrease, while the solvation free energy remains continuous.

cond-mat.soft↗

Polymer chain collapse induced by many-body dipole correlations

We present a simple analytical theory of flexible polymer chain dissolved in a good solvent, carrying permanent freely oriented dipoles on the monomers. We take into account the dipole correlations within the random phase approximation (RPA), as well as a dielectric heterogeneity in the internal polymer volume relative to the bulk solution. We demonstrate that the dipole correlations of monomers can be taken into account as pairwise ones only when the polymer chain is in a coil conformation. In this case the dipole correlations manifest themselves through the Keesom interactions of the permanent dipoles. On the other hand, the dielectric heterogeneity effect (dielectric mismatch effect) leads to effective interaction between the monomers of the polymeric coil. Both of these effects can be taken into account by the renormalizing the second virial coefficient of the volume interactions monomer-monomer. We establish that in the case when the solvent dielectric permittivity exceeds the dielectric permittivity of the polymeric material, the dielectric mismatch effect competes with the dipole attractive interactions, leading to polymer coil expansion. In the opposite case, both the dielectric mismatch effect and the dipole attractive interaction lead to the polymer coil collapse. We analyse the coil-globule transition caused by the dipole correlations of monomers within the many-body theory. We demonstrate that accounting for the dipole correlations higher than pairwise ones smooths this pure electrostatics driven coil-globule transition of the polymer chain.

cond-mat.soft↗

Polarizable polymer chain under external electric field: Effects of many-body electrostatic dipole correlations

We present a new simple self-consistent field theory of the polarizable flexible polymer chain under the external constant electric field with account for the many-body electrostatic dipole correlations. We show the effect of electrostatic dipole correlations on the electric field-induced globule-coil transition. We demonstrate that only when the polymer chain is in the coil conformation, the electrostatic dipole correlations of monomers can be considered as pairwise. However, when the polymer chain is in collapsed state, the dipole correlations have to be considered at the many-body level.

cond-mat.soft↗

On a new application of the path integrals in polymer statistical physics

We propose a new approach based on the path integral formalism to the calculation of the probability distribution functions of quadratic quantities of the Gaussian polymer chain in d-dimensional space, such as the radius of gyration and potential energy in the parabolic well. In both cases we obtain the exact relations for the characteristic function and cumulants. Using the standard steepest-descent method, we evaluate the probability distribution functions in two limiting cases of the large and small values of corresponding variables.

cond-mat.soft↗

A statistical theory of coil-to-globule-to-coil transition of a polymer chain in the mixture of good solvents

We present an off-lattice statistical model of a single polymer chain in mixed solvent media. Taking into account a polymer conformational entropy, renormalization of solvent composition near the polymer backbone, the universal intermolecular excluded volume and Van-der-Waals interactions within the self-consistent field theory the reentrant coil-to-globule-to-coil transition (co-nonsolvency) has been described in this paper. For convenience we split the system volume in two parts: the volume occupied by the polymer chain and the volume of bulk solution. Considering the equilibrium between two sub-volumes, the polymer solvation free energy as a function of radius of gyration and co-solvent mole fraction within internal polymer volume has been obtained. Minimizing the free energy of solvation with respect to its arguments, we show two qulitatively different regimes of co-nonsolvency. Namely, at sufficiently high temperature a reentrant coil-to-globule-to-coil transition proceeds smoothly. On the contrary, when the temperature drops below a certain threshold value a coil-globule transition occurs in the regime of first-order phase transition, i.e., discontinuous changes of the radius of gyration and the local co-solvent mole fraction near the polymer backbone. We show that, when the collapse of polymer chain takes place, the entropy and enthalpy contributions to the solvation free energy of globule strongly grow. From the first principles of statistical thermodynamics we confirm earlier speculations based on the MD simulations results that the co-nonsolvency is the essentially enthalpic-entropic effect and caused by enthalpy-entropy compensation. We show that the temperature dependences of solution heat capacity change due to the solvation of polymer chain are in qualitative agreement with the Differential scanning calorimetry data for PNIPAM in aqueous methanol.

cond-mat.soft↗

On the theory of electric double layer with explicit account of a polarizable co-solvent

We present a continuation of our theoretical research into the influence of co-solvent polarizability on a differential capacitance of the electric double layer [EPL 111, 28002 (2015)]. We formulate a modified Poisson-Boltzmann theory, using the formalism of density functional approach on the level of local density approximation taking into account the electrostatic interactions of ions and co-solvent molecules as well as their excluded volume. We derive the modified Poisson-Boltzmann equation, considering the three-component symmetric lattice gas model as a reference system and minimizing the grand thermodynamic potential with respect to the electrostatic potential. We apply present modified Poisson-Boltzmann equation to the electric double layer theory.

cond-mat.soft↗

Polarizable polymer chain under external electric field in a dilute polymer solution

We study the conformational behavior of polarizable polymer chain under an external homogeneous electric field within the Flory type self-consistent field theory. We consider the influence of electric field on the polymer coil as well as on the polymer globule. We show that when the polymer chain conformation is a coil, application of external electric field leads to its additional swelling. However, when the polymer conformation is a globule, a sufficiently strong field can induce a globule-coil transition. We show that such $"$field-induced$"$ globule-coil transition at the sufficiently small monomer polarizabilities goes quite smoothly. On the contrary, when the monomer polarizability exceeds a certain threshold value, the globule-coil transition occurs as a dramatic expansion in the regime of first-order phase transition. The developed theoretical model can be applied to predicting polymer globule density change under external electric field in order to provide more efficient processes of polymer functionalization, such as sorption, dyeing, chemical modification, etc.

cond-mat.soft↗

A new equation of state of a flexible-chain polyelectrolyte solution: Phase equilibria and osmotic pressure in the salt-free case

We develop a first-principle equation of state of salt-free polyelectrolyte solution in the limit of infinitely long flexible polymer chains in the framework of a field-theoretical formalism beyond the linear Debye-Hueckel theory and predict a liquid-liquid phase separation induced by a strong correlation attraction. As a reference system we choose a set of two subsystems - charged macromolecules immersed in a structureless oppositely charged background created by counterions (polymer one component plasma) and counterions immersed in oppositely charged background created by polymer chains (hard-core one component plasma). We calculate the excess free energy of polymer one component plasma in the framework of Modified Random Phase Approximation, whereas a contribution of charge densities fluctuations of neutralizing backgrounds we evaluate at the level of Gaussian approximation. We show that our theory is in a very good agreement with the results of Monte-Carlo and MD simulations for critical parameters of liquid-liquid phase separation and osmotic pressure in a wide range of monomer concentration above the critical point, respectively.

cond-mat.soft↗

The Equation of State for Solution of Semiflexible Polymer Chains

We formulate a self-consistent procedure for calculation of thermodynamic and structural properties of polymer solutions based on the Gaussian equivalent representation method (GER) for functional integrals calculation beyond the mean-field approximaton. We show that an equation of state, potential of mean force of interaction monomer-monomer, and persistent length should be defined self-consistently by solving of some system of coupled equation.

cond-mat.stat-mech↗