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We present a new time-dependent density functional approach to study the relaxational dynamics of an assembly of interacting particles subject to thermal noise. Starting from the Langevin stochastic equations of motion for the velocities of the particles we are able by means of an approximated closure to derive a self-consistent deterministic equation for the temporal evolution of the average particle density. The closure is equivalent to assuming that the equal-time two-point correlation function out of equilibrium has the same properties as its equilibrium version. The changes in time of the density depend on the functional derivatives of the grand canonical free energy functional F[ρ] of the system. In particular the static solutions of the equation for the density correspond to the exact equilibrium profiles provided one is able to determine the exact form of F[ρ]. In order to assess the validity of our approach we performed a comparison between the Langevin dynamics and the dynamic density functional method for a one-dimensional hard-rod system in three relevant cases and found remarkable agreement, with some interesting exceptions, which are discussed and explained. In addition, we consider the case where one is forced to use an approximate form of F[ρ]. Finally we compare the present method with the stochastic equation for the density proposed by other authors [Kawasaki, Kirkpatrick etc.] and discuss the role of the thermal fluctuations.

We present a new time-dependent Density Functional approach to study the relaxational dynamics of an assembly of interacting particles subject to thermal noise. Starting from the Langevin stochastic equations of motion for the velocities of the particles we are able by means of an approximated closure to derive a self-consistent deterministic equation for the temporal evolution of the average particle density. The closure is equivalent to assuming that the equal-time two-point correlation function out of equilibrium has the same properties as its equilibrium version. The changes in time of the density depend on the functional derivatives of the grand canonical free energy functional F [ρ] of the system. In particular the static solutions of the equation for the density correspond to the exact equilibrium profiles provided one is able to determine the exact form of F [ρ]. In order to assess the validity of our approach we performed a comparison between the Langevin dynamics and the dynamic density functional method for a one-dimensional hard-rod system in three relevant cases and found remarkable agreement, with some interesting exceptions, which are discussed and explained. In addition, we consider the case where one is forced to use an approximate form of F [ρ]. Finally we compare the present method with the stochastic equation for the density proposed by other authors [Kawasaki,Kirkpatrick etc.] and discuss the role of the thermal fluctuations.

We derive the stationary probability distribution for a non-equilibrium system composed by an arbitrary number of degrees of freedom that are subject to Gaussian colored noise and a conservative potential. This is based on a multidimensional version of the Unified Colored Noise Approximation. By comparing theory with numerical simulations we demonstrate that the theoretical probability density quantitatively describes the accumulation of active particles around repulsive obstacles. In particular, for two particles with repulsive interactions, the probability of close contact decreases when one of the two particle is pinned. Moreover, in the case of isotropic confining potentials, the radial density profile shows a non trivial scaling with radius. Finally we show that the theory well approximates the “pressure” generated by the active particles allowing to derive an equation of state for a system of non-interacting colored noise-driven particles.

Phase transitions at fluid interfaces and in fluids confined in pores have been investigated by means of a density functional approach that treats attractive forces between fluid molecules in mean-field approximation and models repulsive forces by hard-spheres. Two types of approximation were employed for the hard-sphere free energy functional: (a)tile well-known local density approximation (LDA) that omits short-ranged correlations and (b) a non-local smoothed density approximation (SDA) that includes such correlations and therefore accounts for the oscillations of the density profile near walls. Three different kinds of phase transition were considered: (i) wetting transition. The transition from partial to complete wetting at a single adsorbing wall is shifted to lower temperatures and tends to become first-order when the more-realistic SDA is employed. Comparison of the results suggests that the LDA overestimates the contact angle 0 in a partial wetting situation. (ii) capillary evaporation of a fluid confined between two parallel hard walls. This transition, from dense 'liquid' to dilute 'gas', occurs in a supersaturated fluid (p > Psat)" The lines of capillary coexistence calculated in the LDA and SDA are rather close, suggesting that non-local effects are not especially important in this case. (iii) capillary condensation of fluids confined between two adsorbing walls or in a single cylindrical pore. For a partial wetting situation the condensation pressures p(