No Arabic abstract
The theory of quasi-neutral equilibrium states of charges above liquid dielectric surface is built. This theory is based on first principles of quantum statistics for systems, comprising many identical particles. The proposed approach is concerned with applying the variation principle, modified for the considered systems, and the Thomas-Fermi model. In terms of the developed theory a self-consistency equations are obtained. These equations provide the relation between the main parameters, describing the system: the potential of static electric field, the distribution function of charges and the surface profile of liquid dielectric. The equations are used to study the phase transition in the system to a spatially periodic state. The proposed method can be applied to analyzing the properties of the phase transition in the system to a spatially periodic states of wave type. Using the analytical and numerical methods, we make a detailed research of the dependence of critical parameters of such phase transition on the thickness of liquid dielectric film. Some stability criteria of the new asymmetric phase of the studied system are discussed.
A theory of equilibrium states of electrons above a liquid helium surface in the presence of an external clamping field is built based on the first principles of quantum statistics for the system of many identical Fermi-particles. The approach is based on the variation principle modified for the considered system and on Thomas-Fermi model. In terms of the developed theory we obtain the self-consistency equations that connect the parameters of the system description, i.e., the potential of a static electric field, the distribution function of electrons and the surface profile of a liquid dielectric. The equations are used to study the phase transition of the system to a spatially periodic state. To demonstrate the capabilities of the proposed method, the characteristics of the phase transition of the system to a spatially periodic state of a trough type are analyzed.
We demonstrate the accurate calculation of entropies and free energies for a variety of liquid metals using an extension of the two phase thermodynamic (2PT) model based on a decomposition of the velocity autocorrelation function into gas-like (hard sphere) and solid-like (harmonic) subsystems. The hard sphere model for the gas-like component is shown to give systematically high entropies for liquid metals as a direct result of the unphysical Lorentzian high-frequency tail. Using a memory function framework we derive a generally applicable velocity autocorrelation and frequency spectrum for the diffusive component which recovers the low frequency (long time) behavior of the hard sphere model while providing for realistic short time coherence and high frequency tails to the spectrum. This approach provides a significant increase in the accuracy of the calculated entropies for liquid metals and is compared to ambient pressure data for liquid sodium, aluminum, gallium, tin, and iron. The use of this method for the determination of melt boundaries is demonstrated with a calculation of the high pressure bcc melt boundary for sodium. With the significantly improved accuracy available with the memory function treatment for softer interatomic potentials, the 2PT model for entropy calculations should find broader application in high energy density science, warm dense matter, planetary science, geophysics, and material science.
We examine the problem of how excited populations of electrons relax after they have been excited by a pump. We include three of the most important relaxation processes: (i) impurity scattering; (ii) Coulomb scattering; and (iii) electron-phonon scattering. The relaxation of an excited population of electrons is one of the most fundamental processes measured in pump/probe experiments, but its interpretation remains under debate. We show how several common assumptions about non-equilibrium relaxation that are pervasive in the field may not hold under quite general conditions. The analysis shows that non-equilibrium relaxation is more complex than previously thought, but it yields to recently developed theoretical methods in non-equilibrium theory. In this work, we show how one can use many-body theory to properly interpret and analyze these complex systems. We focus much of the discussion on implications of these results for experiment.
In this work we investigate the late-time stationary states of open quantum systems coupled to a thermal reservoir in the strong coupling regime. In general such systems do not necessarily relax to a Boltzmann distribution if the coupling to the thermal reservoir is non-vanishing or equivalently if the relaxation timescales are finite. Using a variety of non-equilibrium formalisms valid for non-Markovian processes, we show that starting from a product state of the closed system = system + environment, with the environment in its thermal state, the open system which results from coarse graining the environment will evolve towards an equilibrium state at late-times. This state can be expressed as the reduced state of the closed system thermal state at the temperature of the environment. For a linear (harmonic) system and environment, which is exactly solvable, we are able to show in a rigorous way that all multi-time correlations of the open system evolve towards those of the closed system thermal state. Multi-time correlations are especially relevant in the non-Markovian regime, since they cannot be generated by the dynamics of the single-time correlations. For more general systems, which cannot be exactly solved, we are able to provide a general proof that all single-time correlations of the open system evolve to those of the closed system thermal state, to first order in the relaxation rates. For the special case of a zero-temperature reservoir, we are able to explicitly construct the reduced closed system thermal state in terms of the environmental correlations.
We investigate the dynamics of thermal Casimir interactions between plates described within a living conductor model, with embedded mobile anions and cations, whose density field obeys a stochastic partial differential equation which can be derived starting from the Langevin equations of the individual particles. This model describes the thermal Casimir interaction in the same way that the fluctuating dipole model describes van der Waals interactions. The model is analytically solved in a Debye-Huckel-like approximation. We identify several limiting dynamical regimes where the time dependence of the thermal Casimir interactions can be obtained explicitly. Most notably we find a regime with diffusive scaling, even though the charges are confined to the plates and do not diffuse into the intervening space, which makes the diffusive scaling difficult to anticipate and quite unexpected on physical grounds.