arXiv subjects

James F. Lutsko

Publications and source records attributed to James F. Lutsko.

At least 55 records · Page 3Linked to original sources

arXiv2009

Phase behavior of a confined nano-droplet in the grand-canonical ensemble: the reverse liquid-vapor transition

The equilibrium density distribution and thermodynamic properties of a Lennard-Jones fluid confined to nano-sized spherical cavities at constant chemical potential was determined using Monte Carlo simulations. The results describe both a single cavity with semipermeable walls as well as a collection of closed cavities formed at constant chemical potential. The results are compared to calculations using classical Density Functional Theory (DFT). It is found that the DFT calculations give a quantitatively accurate description of the pressure and structure of the fluid. Both theory and simulation show the presence of a ``reverse'' liquid-vapor transition whereby the equilibrium state is a liquid at large volumes but becomes a vapor at small volumes.

cond-mat.mes-hall↗

arXiv2009

Microscopic and Macroscopic Stress with Gravitational and Rotational Forces

Many recent papers have questioned Irving and Kirkwood's atomistic expression for stress. In Irving and Kirkwood's approach both interatomic forces and atomic velocities contribute to stress. It is the velocity-dependent part that has been disputed. To help clarify this situation we investigate [1] a fluid in a gravitational field and [2] a steadily rotating solid. For both problems we choose conditions where the two stress contributions, potential and kinetic, are significant. The analytic force-balance solutions of both these problems agree very well with a smooth-particle interpretation of the atomistic Irving-Kirkwood stress tensor.

nlin.CD↗

arXiv2009

Is the Tsallis entropy stable?

The question of whether the Tsallis entropy is Lesche-stable is revisited. It is argued that when physical averages are computed with the escort probabilities, the correct application of the concept of Lesche-stability requires use of the escort probabilities. As a consequence, as shown here, the Tsallis entropy is unstable but the thermodynamic averages are stable. We further show that Lesche stability as well as thermodynamic stability can be obtained if the homogeneous entropy is used as the basis of the formulation of non-extensive thermodynamics. In this approach, the escort distribution arises naturally as a secondary structure.

cond-mat.stat-mech↗

arXiv2008

Density Functional Theory of Inhomogeneous Liquids: III. Liquid-Vapor Nucleation

The process of nucleation of vapor bubbles from a superheated liquid and of liquid droplets from a supersaturated vapor is investigated using the Modified-Core van der Waals model Density Functional Theory (Lutsko, JCP 128, 184711 (2008)). A novel approach is developed whereby nucleation is viewed as a transition from a metastable state to a stable state via the minimum free energy path which is identified using the nudged elastic-band method for exploring free energy surfaces. This allows for the unbiased calculation of the properties of sub- and super-critical clusters, as well as of the critical cluster. For Lennard-Jones fluids, the results compare well to simulation and support the view that even at high supersaturation nucleation proceeds smoothly rather than via spinodal-like instabilities as has been suggested recently.

cond-mat.stat-mech↗

arXiv2008

Theoretical description of the nucleation of vapor bubbles in a superheated fluid

The nucleation of vapor bubbles within a superheated fluid is studied using density functional theory. The nudged elastic band technique is used to find the minimum energy pathway from the metastable uniform liquid to the stable uniform gas thus emphasizing the analogy between the the nucleation problem and that of chemical reactions. The result is both an accurate determination of the critical nucleus and an unbiased description of the density profile at various points along the path between the free energy extrema. This calculation is compared to two other methods: the use of parametrized profiles and constrained minimization of the free energy. The results indicate that the recent claim, based on the constraint method, that bubble nucleation and growth involves an activated instability is incorrect.

cond-mat.stat-mech↗

arXiv2008

Dependence of the liquid-vapor surface tension on the range of interaction: a test of the law of corresponding states

The planar surface tension of coexisting liquid and vapor phases of a fluid of Lennard-Jones atoms is studied as a function of the range of the potential using both Monte Carlo simulations and Density Functional Theory. The interaction range is varied from $r_c^* = 2.5$ to $r_c^* = 6$ and the surface tension is determined for temperatures ranging from $T^* = 0.7$ up to the critical temperature in each case. The results are shown to be consistent with previous studies. The simulation data are well-described by Guggenheim's law of corresponding states but the agreement of the theoretical results depends on the quality of the bulk equation of state.

cond-mat.stat-mech↗

arXiv2008

Density Functional Theory of Inhomogeneous Liquids: II. A Fundamental Measure Approach

Previously, it has been shown that the direct correlation function for a Lennard-Jones fluid could be modeled by a sum of that for hard-spheres, a mean-field tail and a simple linear correction in the core region constructed so as to reproduce the (known) bulk equation of state of the fluid(Lutsko, JCP 127, 054701 (2007)). Here, this model is combined with ideas from Fundamental Measure Theory to construct a density functional theory for the free energy. The theory is shown to accurately describe a range of inhomogeneous conditions including the liquid-vapor interface, the fluid in contact with a hard wall and a fluid confined in a slit pore. The theory gives quantitatively accurate predictions for the surface tension, including its dependence on the potential cutoff. It also obeys two important exact conditions: that relating the direct correlation function to the functional derivative of the free energy with respect to density, and the wall theorem.

cond-mat.stat-mech↗

arXiv2007

Generalized Diffusion

The Fokker-Planck equation for the probability $f(r,t)$ to find a random walker at position $r$ at time $t$ is derived for the case that the the probability to make jumps depends nonlinearly on $f(r,t)$. The result is a generalized form of the classical Fokker-Planck equation where the effects of drift, due to a violation of detailed balance, and of external fields are also considered. It is shown that in the absence of drift and external fields a scaling solution, describing anomalous diffusion, is only possible if the nonlinearity in the jump probability is of the power law type ($\sim f^{η}(r,t)$), in which case the generalized Fokker-Planck equation reduces to the well-known Porous Media equation. Monte-Carlo simulations are shown to confirm the theoretical results.

cond-mat.stat-mech↗

arXiv2007

Density functional theory of inhomogeneous liquids. I. The liquid-vapor interface in Lennard-Jones fluids

A simple model is proposed for the direct correlation function (DCF) for simple fluids consisting of a hard-core contribution, a simple parametrized core correction, and a mean-field tail. The model requires as input only the free energy of the homogeneous fluid, obtained, e.g., from thermodynamic perturbation theory. Comparison to the DCF obtained from simulation of a Lennard-Jones fluid shows this to be a surprisingly good approximation for a wide range of densities. The model is used to construct a density functional theory for inhomogeneous fluids which is applied to the problem of calculating the surface tension of the liquid-vapor interface. The numerical values found are in good agreement with simulation.

cond-mat.stat-mech↗

arXiv2006

Properties of non-FCC hard-sphere solids predicted by density functional theory

The free energies of the FCC, BCC, HCP and Simple Cubic phases for hard spheres are calculated as a function of density using the Fundamental Measure Theory models of Rosenfeld et al (PRE 55, 4245 (1997)), Tarazona (PRL 84, 694 (2001)) and Roth et al (J. Phys.: Cond. Matt. 14, 12063 (2002)) in the Gaussian approximation. For the FCC phase, the present work confirms the vanishing of the Lindemann parameter (i.e. vanishing of the width of the Gaussians) near close packing for all three models and the results for the HCP phase are nearly identical. For the BCC phase and for packing fractions above $η\sim 0.56$, all three theories show multiple solid structures differing in the widths of the Gaussians. In all three cases, one of these structures shows the expected vanishing of the Lindemann parameter at close packing, but this physical structure is only thermodynamically favored over the unphysical structures in the Tarazona theory and even then, some unphysical behavior persists at lower densities. The simple cubic phase is stabilized in the model of Rosenfeld et al. for a range of densities and in the Tarazona model only very near close-packing.

cond-mat.stat-mech↗

arXiv2006

Ginzburg-Landau theory of the liquid-solid interface and nucleation for hard-spheres

The Ginzburg-Landau free energy functional for hard-spheres is constructed using the Fundamental Measure Theory approach to Density Functional Theory as a starting point. The functional is used to study the liquid-fcc solid planer interface and the properties of small solid clusters nucleating within a liquid. The surface tension for planer interfaces agrees well with simulation and it is found that the properties of the solid clusters are consistent with classical nucleation theory.

cond-mat.stat-mech↗

arXiv2005

Chapman-Enskog expansion about nonequilibrium states: the sheared granular fluid

The Chapman-Enskog method of solution of kinetic equations, such as the Boltzmann equation, is based on an expansion in gradients of the deviations fo the hydrodynamic fields from a uniform reference state (e.g., local equilibrium). This paper presents an extension of the method so as to allow for expansions about \emph{arbitrary}, far-from equilibrium reference states. The primary result is a set of hydrodynamic equations for studying variations from the arbitrary reference state which, unlike the usual Navier-Stokes hydrodynamics, does not restrict the reference state in any way. The method is illustrated by application to a sheared granular gas which cannot be studied using the usual Navier-Stokes hydrodynamics.

cond-mat.stat-mech↗

arXiv2005

Hydrodynamics of an inelastic gas with implications for sonochemistry

The hydrodynamics for a gas of hard-spheres which sometimes experience inelastic collisions resulting in the loss of a fixed, velocity-independent, amount of energy $Δ$ is investigated with the goal of understanding the coupling between hydrodynamics and endothermic chemistry. The homogeneous cooling state of a uniform system and the modified Navier-Stokes equations are discussed and explicit expressions given for the pressure, cooling rates and all transport coefficients for D-dimensions. The Navier-Stokes equations are solved numerically for the case of a two-dimensional gas subject to a circular piston so as to illustrate the effects of the enegy loss on the structure of shocks found in cavitating bubbles. It is found that the maximal temperature achieved is a sensitive function of $Δ$ with a minimum occuring near the physically important value of $Δ\sim 12,000K \sim 1eV$

cond-mat.soft↗

arXiv2005

Theoretical evidence for a dense fluid precursor to crystallization

We present classical density functional theory calculations of the free energy landscape for fluids below their triple point as a function of density and crystallinity. We find that for both a model globular protein and for a simple atomic fluid modeled with a Lennard-Jones interaction, it is free-energetically easier to crystallize by passing through a metastable dense fluid in accord with the Ostwald rule of stages but in contrast to the alternative of ordering and densifying at once as assumed in the classical picture of crystallization.

cond-mat.stat-mech↗

arXiv2005

First Principles Derivation of Effective Ginzburg-Landau Free Energy models for Crystalline Systems

The expression of the free energy density of a classical crystalline system as a gradient expansion in terms of a set of order parameters is developed using classical density functional theory. The goal here is to extend and complete an earlier derivation by L{ö}wen et al (Europhys. Lett.9, 791, 1989). The limitations of the resulting expressions are also discussed including the boundary conditions needed for finite systems and the fact that the results cannot, at present, be used to take into account elastic relaxation.

cond-mat.stat-mech↗

arXiv2005

Generalized diffusion equation

Modern analyses of diffusion processes have proposed nonlinear versions of the Fokker-Planck equation to account for non-classical diffusion. These nonlinear equations are usually constructed on a phenomenological basis. Here we introduce a nonlinear transformation by defining the $q$-generating function which, when applied to the intermediate scattering function of classical statistical mechanics, yields, in a mathematically systematic derivation, a generalized form of the advection-diffusion equation in Fourier space. Its solutions are discussed and suggest that the $q$-generating function approach should be a useful tool to generalize classical diffusive transport formulations.

cond-mat.stat-mech↗

arXiv2005

Nonextensive diffusion as nonlinear response

The porous media equation has been proposed as a phenomenological ``non-extensive'' generalization of classical diffusion. Here, we show that a very similar equation can be derived, in a systematic manner, for a classical fluid by assuming nonlinear response, i.e. that the diffusive flux depends on gradients of a power of the concentration. The present equation distinguishes from the porous media equation in that it describes \emph{% generalized classical} diffusion, i.e. with $r/\sqrt Dt$ scaling, but with a generalized Einstein relation, and with power-law probability distributions typical of nonextensive statistical mechanics.

cond-mat.stat-mech↗

arXiv2005

The effect of the range of interaction on the phase diagram of a globular protein

Thermodynamic perturbation theory is applied to the model of globular proteins studied by ten Wolde and Frenkel (Science 277, pg. 1976) using computer simulation. It is found that the reported phase diagrams are accurately reproduced. The calculations show how the phase diagram can be tuned as a function of the lengthscale of the potential.

physics.bio-ph↗