No Arabic abstract
Self-diffusion and radial distribution functions are studied in a strongly confined Lennard-Jones fluid. Surprisingly, in the solid-liquid phase transition region, where the system exhibits dynamic coexistence, the self-diffusion constants are shown to present up to three-fold variations from solid to liquid phases at fixed temperature, while the radial distribution function corresponding to both the liquid and the solid phases are essentially indistinguishable.
We use an analytic criterion for vanishing of exponential damping of correlations developed previously (Piasecki et al, J. Chem. Phys., 133, 164507, 2010) to determine the threshold volume fractions for structural transitions in hard sphere systems in dimensions D=3,4,5 and 6, proceeding from the YBG hierarchy and using the Kirkwood superposition approximation. We conclude that the theory does predict phase transitions in qualitative agreement with numerical studies. We also derive, within the superposition approximation, the asymptotic form of the analytic condition for occurence of a structural transition in the D->Infinity limit .
We revisit motility-induced phase separation in two models of active particles interacting by pairwise repulsion. We show that the resulting dense phase contains gas bubbles distributed algebraically up to a typically large cutoff scale. At large enough system size and/or global density, all the gas may be contained inside the bubbles, at which point the system is microphase-separated with a finite cut-off bubble scale. We observe that the ordering is anomalous, with different dynamics for the coarsening of the dense phase and of the gas bubbles. This phenomenology is reproduced by a reduced bubble model that implements the basic idea of reverse Ostwald ripening put forward in Tjhung et al. [Phys. Rev. X 8, 031080 (2018)].
Flory-Huggins theory is a mean field theory for modelling the free energy of dense polymer solutions and polymer melts. In this paper we use Flory-Huggins theory as a model of a dense two dimensional self-avoiding walk confined to a square in the square lattice. The theory describes the free energy of the walk well, and we estimate the Flory interaction parameter of the walk to be $chi_{saw} = 0.32(1)$.
In this report, an analytic model to predict phase transitions of confined fluids in nano systems is presented and it is used to predict the behavior of the confined fluid in nanotubes and nanoslits. In our approach besides including a third degree of freedom due to wall effect to define the state of the system, the tensorial character for pressure is considered. Using the perturbation theory of statistical mechanics it is shown that the van der Waals equation of state is equally valid for small as well as large systems. The model proposed is shown to predict the liquid-vapor phase transition as well as the critical point in any size confined fluid systems. It is also shown that the critical temperature increases with the size of the nano system and finally it reaches the macroscopic critical temperature value as the diameter of the nanotube (or width of the nanoslit) approaches infinity. The proposed model can also demonstrate the existence of the local density and phase fragmentations during phase transitions in a confined nano system.
Presenting simple coarse-grained models of isotropic solids and fluids in $d=1$, $2$ and $3$ dimensions we investigate the correlations of the instantaneous pressure and its ideal and excess contributions at either imposed pressure (NPT-ensemble, $lambda=0$) or volume (NVT-ensemble, $lambda=1$) and for more general values of the dimensionless parameter $lambda$ characterizing the constant-volume constraint.