173 research outputs found
Probing the existence of phase transitions in one-dimensional fluids of penetrable particles
No full textPhase transitions in one-dimensional classical fluids are usually ruled out by using van Hove's theorem. A way to circumvent the conclusions of the theorem is to consider an interparticle potential that is everywhere bounded. Such is the case of, e.g., the generalized exponential model of index 4 (GEM-4 potential), which in three dimensions gives a reasonable description of the effective repulsion between flexible dendrimers in a solution. An extensive Monte Carlo simulation of the one-dimensional GEM-4 model [S. Prestipino, Phys. Rev. E 90, 042306 (2014)PLEEE81539-375510.1103/PhysRevE.90.042306] has recently provided evidence of an infinite sequence of low-temperature cluster phases, however, also suggesting that upon pushing the simulation forward what seemed a true transition may eventually prove to be only a sharp crossover. We hereby investigate this problem theoretically by use of three different and increasingly sophisticated approaches (i.e., a mean-field theory, the transfer matrix of a lattice model of clusters, and the exact treatment of a system of point clusters in the continuum) to conclude that the alleged transitions of the one-dimensional GEM-4 system are likely just crossovers.Phase transitions in one-dimensional classical fluids are usually ruled out by making appeal to van Hove’s theorem. A way to circumvent the conclusions of the theorem is to consider an interparticle potential that is everywhere bounded. Such is the case of, e.g., the generalized exponential model of index 4 (GEM-4 potential), which in three dimensions gives a reasonable description of the effective repulsion between flexible dendrimers in a solution. An extensive Monte Carlo simulation of the one-dimensional GEM-4 model [S. Prestipino, Phys. Rev. E 90, 042306 (2014)] has recently provided evidence of an infinite sequence of low-temperature cluster phases, however also suggesting that upon pushing the simulation forward what seemed a true transition may eventually prove to be only a sharp crossover. We hereby investigate this problem theoretically, by three different and increasingly sophisticated approaches (i.e., a mean-field theory, the transfer matrix of a lattice model of clusters, and the exact treatment of a system of point clusters in the continuum), to conclude that the alleged transitions of the one-dimensional GEM4 system are likely just crossovers
Kink-kink interactions and pre-roughening of vicinal surfaces
No full textThermal anisotropic roughening of vicinal surfaces is well known and well studied. Here, we consider the possibility that a separate pre-roughening transition might take place, prior to roughening. Within the framework of a terrace-step-kink model, we identify possible interaction mechanisms for promoting pre-roughening (PR) and the ensuing disordered flat (DOF) phase. In particular, the most likely to occur in real systems is a short-range repulsion between equally oriented parallel kinks. When this interaction is strong, PR shows up and the DOF phase is characterized by antiparallel order of kinks within a step. Next, we discuss the relevance of this scenario for real vicinals, in particular Ag(115), where high-accuracy scanning tunnelling microscopy data are available
Preroughening, Diffusion, and Growth of a fcc(111) Surface
No full textPreroughening of close-packed fcc(111) surfaces, found in rare gas solids, is an interesting but poorly characterized phase transition. We introduce a restricted solid-on-solid model, which describes it. Using mostly Monte Carlo, we study both statics, including critical behavior and scattering properties, and dynamics, including surface diffusion and growth. In antiphase scattering, it is shown that preroughening will generally show up at most as a dip. Surface growth is predicted to be continuous at preroughening, where surface self-diffusion should also drop. The physical mechanism leading to preroughening on rare gas surfaces is analyzed and identified in the step-step elastic repulsion
Systematic Improvement of Classical Nucleation Theory
No full textWe reconsider the applicability of classical nucleation theory (CNT) to the calculation of the free energy of solid cluster formation in a liquid and its use to the evaluation of interface free energies from nucleation barriers. Using two different freezing transitions (hard spheres and NaCl) as test cases, we first observe that the interface-free-energy estimates based on CNT are generally in error. As successive refinements of nucleation-barrier theory, we consider corrections due to a nonsharp solid-liquid interface and to a nonspherical cluster shape. Extensive calculations for the Ising model show that corrections due to a nonsharp and thermally fluctuating interface account for the barrier shape with excellent accuracy. The experimental solid nucleation rates that are measured in colloids are better accounted for by these non-CNT terms, whose effect appears to be crucial in the interpretation of data and in the extraction of the interface tension from them
A fingerprint of surface-tension anisotropy in the free-energy cost of nucleation
No full textWe focus on the Gibbs free energy ΔG for nucleating a droplet of the stable phase (e.g. solid) inside the metastable parent phase (e.g. liquid), close to the first-order transition temperature. This quantity is central to the theory of homogeneous nucleation, since it superintends the nucleation rate. We recently introduced a field theory describing the dependence of ΔG on the droplet volume V, taking into account besides the microscopic fuzziness of the droplet-parent interface, also small fluctuations around the spherical shape whose effect, assuming isotropy, was found to be a characteristic logarithmic term. Here we extend this theory, introducing the effect of anisotropy in the surface tension, and show that in the limit of strong anisotropy ΔG(V) once more develops a term logarithmic on V, now with a prefactor of opposite sign with respect to the isotropic case. Based on this result, we argue that the geometrical shape that large solid nuclei mostly prefer could be inferred from the prefactor of the logarithmic term in the droplet free energy, as determined from the optimization of its near-coexistence profile
Shape and area fluctuation effects on nucleation theory
No full textIn standard nucleation theory, the nucleation process is characterized by computing ΔΩ(V), the reversible work required to form a cluster of volume V of the stable phase inside the metastable mother phase. However, other quantities besides the volume could play a role in the free energy of cluster formation, and this will in turn affect the nucleation barrier and the shape of the nucleus. Here we exploit our recently introduced mesoscopic theory of nucleation to compute the free energy cost of a nearly spherical cluster of volume V and a fluctuating surface area A, whereby the maximum of ΔΩ(V) is replaced by a saddle point in ΔΩ(V, A). Compared to the simpler theory based on volume only, the barrier height of ΔΩ(V, A) at the transition state is systematically larger by a few kBT. More importantly, we show that, depending on the physical situation, the most probable shape of the nucleus may be highly non-spherical, even when the surface tension and stiffness of the model are isotropic. Interestingly, these shape fluctuations do not influence or modify the standard Classical Nucleation Theory manner of extracting the interface tension from the logarithm of the nucleation rate near coexistence
Preroughening, and disordered flat phase separation in surface molecular dynamics simulations
No full text- …
