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Entropy

Energetic Cost of Statistical Order-Degree Change in a Fermions’ Set

F. Pennini, Angelo Plastino, G.L. Ferri, Angel Ricardo Plastino

Published May 26, 2022• 1 citation
Publisher

Abstract

We discuss novel many-fermions thermodynamics' features. They refer to the energy cost associated to order-disorder changes. Our thermal quantum statistical scenario is controlled by suitable fermion-fermion interactions. We deal with two well-known quantum interactions that operate within an exactly solvable model. This model is able to adequately describe some aspects of fermion-dynamics, particularly level-crossings. We describe things via employment of Gibbs' canonical ensemble strictures. We show that judicious manipulation of the energy cost associated to statistical order (disorder) variations generates useful information-quantifiers. The underlying idea is that changes in the degree of order are intimately linked to level-crossings energetic costs.

DOI
10.3390/e24060752

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•Jan 1, 2009•0 citations
We discuss novel many-fermions thermodynamics' features. They refer to the energy cost associated to order-disorder changes. Our thermal quantum statistical scenario is controlled by suitable fermion-fermion interactions. We deal with two well-known quantum interactions that operate within an exactly solvable model. This model is able to adequately describe some aspects of fermion-dynamics, particularly level-crossings. We describe things via employment of Gibbs' canonical ensemble strictures. We show that judicious manipulation of the energy cost associated to statistical order (disorder) variations generates useful information-quantifiers. The underlying idea is that changes in the degree of order are intimately linked to level-crossings energetic costs.
We deal here with the notion of statistical order and apply it to a system of interacting fermions endowed with an SU2 × SU2 symmetry. The discussion takes place in a thermal quantum statistical scenario. Two distinct fermion–fermion interactions are at play. One of them is a well-known spin–flip interaction. The other is the pairing interaction responsible for nuclear superconductivity. We used novel statistical quantifiers that yield insights regarding changes in the statistical order produced when the values of the pertinent coupling constants vary. In particular, we show that judicious manipulation of the energy cost associated with statistical order variations with the fermion number is the key to understanding important details of the associated dynamics.
The objective of this work is to show that simple modifications in the form of the fermion–fermion interacting potential generate widely different thermodynamic behaviors, with macroscopic manifestations reflected by the thermal free energy. This is done by appealing to quantum statistical mechanics, in its Gibbs’ ensemble formalism, employing two different SU2 exactly solvable models. Some intriguing aspects of the fermion dynamics are uncovered. We conclude that, in investigating fermion dynamics, minute changes in the Hamiltonian may lead to dramatic consequences in the behavior of the Helmholtz’ free energy.
This work scrutinizes, using statistical mechanics indicators, important traits displayed by quantum many-body systems. Our statistical mechanics quantifiers are employed, in the context of Gibbs’ canonical ensemble at temperature T. A new quantifier of this sort is also presented here. The present discussion focuses attention on the role played by the fermion number N in many-fermion dynamics, that is, N is our protagonist. We have discovered discovers particular values of N for which the thermal indicators exhibit unexpected abrupt variations. Such a fact reflects an unanticipated characteristic of fermionic dynamics.
Beginning with Mandelbrot’s insight that Fisher information may admit a thermodynamic interpretation, a growing body of work has connected this information-theoretic measure to fluctuation–dissipation relations, thermodynamic geometry, and phase transitions. Yet, these connections have largely remained at the level of formal analogies. In this work, we provide what is, to our knowledge, the first explicit realization of the epistemic-to-physical transition of Fisher information within a finite interacting quantum system. Specifically, we analyze a model of N fermions occupying two degenerate levels and coupled by a spin-flip interaction of strength V, treated in the grand canonical ensemble at inverse temperature β. We compute the Fisher information FN(V) associated with the sensitivity of the thermal state to changes in V, and show that it becomes an observer-independent, experimentally meaningful quantity: it encodes fluctuations, tracks entropy variations, and reveals structural transitions induced by interactions. Our findings thus demonstrate that Fisher information, originally conceived as an inferential and epistemic measure, can operate as a bona fide thermodynamic observable in quantum many-body physics, bridging the gap between information-theoretic foundations and measurable physical law.
We investigate the physics of a medium-size quantum particle' gases, of the order of hundreds or thousands of fermions/bosons (far below the thermodynamic limit N → 1024N \, \rightarrow \, 10^{24}N→1024). Appeal to microcanonical ensemble becomes then unavoidable. The so-called statistical complexity is our protagonist. Interesting facts are uncovered, both for fermions and bosons, yielded by statistical quantifiers.
Recently, the possibility of investigating single molecule, or single spin observables, as well as the necessity of a better understanding of the mechanisms underlying quantum dynamics in order to obtain nanoscale devices and nanostructered materials suitable for quantum computing tasks, have revived the interest in foundational aspects of quantum statistical mechanics. This thesis aims to give a contribution to this field by re-considering the statistical characterization of a quantum system at the light of some paradigmatic changes in our understanding of quantum theory which have taken place in the last two decades. In particular the impressive development of quantum information theory has changed the perceptions of quantum entanglement: for a long time it has been considered a somewhat paradoxical property of the matter at the atomic scale, but now it is regarded as an essential and ubiquitous phenomenon whose consequences are affecting the very macroscopic world that we experience. Still the decoherence program has brought out the importance of considering a quantum system together with its environment in order to clarify some key aspects of quantum dynamics. Thus, we start from the idea that quantum correlations are ubiquitous and somewhat uncontrollable in systems with many degrees of freedom which are typically considered in statistical mechanics. As a consequence we assume the standpoint that quantum statistical mechanics has not to be based on the underlying idea of a collection of many, independent quantum systems but rather it has to emerge at the level of a global wavefunction (pure state) which describes the system as well as its environment as a whole. In order to investigate the consequences of these assumptions we study the equilibrium distribution of an isolated quantum system. This is defined, in analogy with the ergodic foundations of classical statistical mechanics, on the basis of the time evolution of the quantum state. Then, we study the emergence of thermodynamic properties in a quantum system by studying the probability distribution of some function of interests, as the entropy and the equilibrium state of a subsystem, on Ensembles of Pure States. Such a probability distribution is derived from the geometry of the Hilbert space, and the theoretical tools suitable for its characterization are developed. On the one hand we perform a numerical sampling of the ensemble distributions by employing Monte Carlo techniques, on the other hand simpler analytical approximation of the geometrical distributions are derived by means of a maximum entropy principle. Model systems composed of an ensemble of spins are chosen to illustrate the salient features which emerge from the developed theoretical framework: the main point is that the Ensemble Distributions of “thermodynamic observables” (entropy or equilibrium state of a subsystem) are sharply peaked around a typical value. From the analysis it emerges that each of the overwhelming majority of the wavefunctions which has appreciable weight in the considered ensemble, is characterized by the same value of the “macroscopic” functions. This is a striking evidence of the “typicality” of these properties. In the essence, our impossibility to know the state of the system in detail does not matter, just for the remarkable fact that almost all quantum states behave essentially in the same way. By virtue of this typicality the study of the behaviour of the typical values of the thermodynamic function become meaningful. Notably, under certain conditions, one recovers the results of standard statistical mechanics, that is, the equilibrium average of the state of a subsystem can be cast in the Boltzmann canonical form at the temperature given by the usual thermodynamical relation . In the second part of the thesis we consider the dynamical aspects of the equilibrium state of a subsystem interacting with its environment. The fluctuations around the equilibrium average critically depends on the entanglement between the system and the environment and on the form of the interaction Hamiltonian. The connection between the dynamics of the fluctuations of an observable at the equilibrium and the relaxation toward the equilibrium from a “non typical” initial value is also investigated with the aid of simple model systems. The study presented in this thesis was partly motivated by a critical analysis of the statistical methods available for the theoretical modelling of magnetic resonance experiments. One of these, the Stochastic Liouville Equation, has been employed in a work completed during the first year of my Ph.D. program in order to interpret some feature of a two dimensional electron spin resonance experiment, [Fresch B., Frezzato D., Moro G. J., Kothe G., Freed J. H.; J. Phys. Chem. B., 110, 24238, (2006)].