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This paper proposes a simple mathematical model of non-stationary and non-linear stochastic dynamics, which approximates a (globally) non-stationary and non-linear stochastic process by its locally (or \emph{"piecewise"}) stationary version. Profiting from the elegance and simplicity of both, the exact mathematical model referred to as the Ornstein-Uhlenbeck stochastic process (which is \emph{globally} stationary, Markov and Gaussian) and of the Lyapunov criterion associated with the stability of stationarity, we show that the proposed non-linear non-stationary model provides a natural extension of the Onsager-Machlup theory of equilibrium thermal fluctuations, to the realm of non-stationary, non-linear, and non-equilibrium processes. As an illustrative application, we then apply the extended non-equilibrium Onsager-Machlup theory, to the description of thermal fluctuations and irreversible relaxation processes in liquids, leading to the main exact equations employed to construct the \emph{non-equilibrium self-consistent generalized Langevin equation} (NE-SCGLE) theory of irreversible processes in liquids. This generic theory has demonstrated that the most intriguing and long-unsolved questions of the glass and the gel transitions are understood as a natural consequence of the second law of thermodynamics, enunciated in terms of the proposed piecewise stationary stochastic mathematical model.

We investigate the structural relaxation of a soft-sphere liquid quenched isochorically ($\phi=0.7$) and instantaneously to different temperatures $T_f$ above and below the glass transition. For this, we combine extensive Brownian dynamics simulations and theoretical calculations based on the non-equilibrium self-consistent generalized Langevin equation (NE-SCGLE) theory. The response of the liquid to a quench generally consists of a sub-linear increase of the $\alpha$-relaxation time with system's age. Approaching the ideal glass-transition temperature from above ($T_f>T^a$) sub-aging appears as a transient process describing a broad equilibration crossover for quenches to nearly arrested states. This allows us to empirically determine an equilibration timescale $t^{eq}(T_f)$ that becomes increasingly longer as $T_f$ approaches $T^a$. For quenches inside the glass ($T_f\leq T^a$) the growth rate of the structural relaxation time becomes progressively larger as $T_f$ decreases and, unlike the equilibration scenario, $\tau_{\alpha}$ remains evolving within the whole observation time-window.These features are consistently found in theory and simulations with remarkable semi-quantitative agreement, and coincide with those revealed in the similar and complementary exercise [Phys. Rev. {\bf 96}, 022608 (2017)] that considered a sequence of quenches with fixed final temperature $T_f=0$ but increasing $\phi$ towards the hard-sphere dynamical arrest volume fraction $\phi^a_{HS}=0.582$. The NE-SCGLE analysis, however, unveils various fundamental aspects of the glass transition, involving the abrupt passage from the ordinary equilibration scenario to the persistent aging effects that are characteristic of glass-forming liquids. The theory also explains that, within the time window of any experimental observation, this can only be observed as a continuous crossover.

A fundamental challenge of the theory of liquids is to understand the similarities and differences in the macroscopic dynamics of both colloidal and atomic liquids, which originate in the (Newtonian or Brownian) nature of the microscopic motion of their constituents. Starting from the recently-discovered long-time dynamic equivalence between a colloidal and an atomic liquid that share the same interparticle pair potential, in this work we develop a self-consistent generalized Langevin equation (SCGLE) theory for the dynamics of equilibrium multicomponent atomic liquids, applicable as an approximate but quantitative theory describing the long-time diffusive dynamical properties of simple equilibrium atomic liquids. When complemented with a Gaussian-like approximation, this theory is also able to provide a reasonable representation of the passage from ballistic to diffusive behavior. We illustrate the applicability of the resulting theory with three particular examples, namely, a monodisperse and a polydisperse monocomponent hard-sphere liquid, and a highly size-asymmetric binary hard-sphere mixture. To assess the quantitative accuracy of our results, we perform event-driven molecular dynamics simulations, which corroborate the general features of the theoretical predictions., Comment: 11 pages, 12 Figures

We derive the time-evolution equation that describes the Brownian motion of labeled individual tracer particles in a simple model atomic liquid (i.e., a system of $N$ particles whose motion is governed by Newton's second law, and interacting through spherically symmetric pairwise potentials). We base our derivation on the generalized Langevin equation formalism, and find that the resulting time evolution equation is formally identical to the generalized Langevin equation that describes the Brownian motion of individual tracer particles in a colloidal suspension in the absence of hydrodynamic interactions. This formal dynamic equivalence implies the long-time indistinguishability of some dynamic properties of both systems, such as their mean squared displacement, upon a well-defined time scaling. This prediction is tested here by comparing the results of molecular and Brownian dynamics simulations performed on the hard sphere system., Comment: 2 figures and 26 pages

We show that the kinetic-theoretical self-diffusion coefficient of an atomic fluid plays the same role as the short-time self-diffusion coefficient D_S in a colloidal liquid, in the sense that the dynamic properties of the former, at times much longer than the mean free time, and properly scaled with D_S, will indistinguishable from those of a colloidal liquid with the same interaction potential. One important consequence of such dynamic equivalence is that the ratio D_L/ D_S of the long-time to the short-time self-diffusion coefficients must then be the same for both, an atomic and a colloidal system characterized by the same inter-particle interactions. This naturally extends to atomic fluids a well-known dynamic criterion for freezing of colloidal liquids[Phys. Rev. Lett. 70, 1557 (1993)]. We corroborate these predictions by comparing molecular and Brownian dynamics simulations on (soft- and hard-sphere) model systems, representative of what we may refer to as the "hard-sphere" dynamic universality class.