The function F{N} which gives the relative probability of a configuration {N} is studied for the case of a quantum-mechanical system to which classical statistics can be applied. By means of a device originally used in quantum electrodynamics F{N} is obtained in a new form which is very closely related to the form of the analogous classical distribution FCL{N}. The new form of F{N} shows clearly how the difference between F{N} and FCL{N} is related to the uncertainty principle. As an illustration of the utility of the methods presented here several applications are presented. The first application is a high temperature development of F{N} as a power series in ℏ/kT which is carried through to the fourth order. The second application is the development of F{N} as a series of configuration space integrals. A previously published low temperature development of F{N} is obtained in a simple manner, and it is shown that all higher terms in the development can be written down explicitly by starting from the new form of F{N}. Finally, several integral equations for F{N} are presented which give physical insight into its structure, by establishing mathematical analogies with such physical processes as neutron diffusion.
The function F{N} which gives the relative probability of a configuration {N} is studied for the case of a quantum-mechanical system to which classical statistics can be applied. By means of a device originally used in quantum electrodynamics F{N} is obtained in a new form which is very closely related to the form of the analogous classical distribution FCL{N}. The new form of F{N} shows clearly how the difference between F{N} and FCL{N} is related to the uncertainty principle. As an illustration of the utility of the methods presented here several applications are presented. The first application is a high temperature development of F{N} as a power series in ℏ/kT which is carried through to the fourth order. The second application is the development of F{N} as a series of configuration space integrals. A previously published low temperature development of F{N} is obtained in a simple manner, and it is shown that all higher terms in the development can be written down explicitly by starting from the new form of F{N}. Finally, several integral equations for F{N} are presented which give physical insight into its structure, by establishing mathematical analogies with such physical processes as neutron diffusion.
The method of functional differentiation, used in classical statistical mechanics to obtain approximate integral equations for the pair distribution function, is extended to quantum systems obeying Maxwell-Boltzmann statistics. The grand partition function is written as a path integral, and space-temperature distributions are generated from it by successive functional differentiation. Distributions can be expanded in powers of an external potential via a functional Taylor series. When the series is truncated so that no distributions higher than second order enter and the external potential is specialized to one arising from a fixed particle in the system, coupled integral equations result for the two kinds of pair distributions. The first-order Ursell function calculated from these equations yields the Montroll-Ward ring summation for the grand potential. This approximate Ursell function determines also the Fourier transform of the momentum density (useful in calculating the p = 0 occupation number). Although divergences appear in the low-temperature limit, they can be removed by a simple modification of the independent functional. An extension to Fermi-Dirac and Böse-Einstein statistics is indicated at appropriate places in the text.
Abstract It is well known that a new form of statistical mechanics has been recently developed by Einstein for an ideal gas of structureless mass-points. This starts from a discussion by Bose of the laws of temperature radiation based on the light quantum hypothesis, and has been further analysed by Schrödinger. Yet another new form has been proposed independently by Fermi and Dirac. The latter based his theory on a discussion of lightly coupled systems with the help of Schrödinger’s equation. Combined with Heisenberg’s work on the many-body problem, Dirac’s work forces us to conclude at least that the classical form of statistical mechanics must be changed. It indicates that the true form, which satisfies the laws of the new mechanics, is almost certainly that of Fermi and Dirac, which is the natural generalization of Pauli’s principle of exclusion for electronic orbits in an atom. The work of Heisenberg and Dirac already quoted has shown that Pauli’s principle and its extension are satisfied in the new mechanics by a complete self-consistent solution of the equations of motion. So far as I am aware, the discussions of the new forms have as yet dealt only with the statistics of a gas of structureless mass-points (and, of course, temperature radiation). There has, moreover, been as yet no attempt to define the entropy (and the absolute temperature) in strict analogy with rational thermodynamics by means of the equation dQ = TdS. If another definition is preferred, then this equation must be deduced from it. It has, therefore, seemed worth while to reopen the discussion by examining ab initio a quite general form of statistical mechanics of which the classical form and instein’s and Fermi-Dirac’s are special cases. This is rendered possible by using the powerful method of complex integration already applied to the classical form. The sequence of the argument is then to take the general form, which covers a very large range of ways of assigning possibilities and counting complexions, and construct on that basis exact integral expressions for the number of complexions possible to the assembly and for the average number of systems of the assembly in their various quantum states. We then derive from these the average energies and external reactions and so the form of dQ, deduce from dQ the existence of S and so define S and T. This can be done in the general form for assemblies of ideal systems just as general as can be handled in the classical way—ideal gases of molecules of any structure and crystals and radiation. Such assemblies are in all cases thermodynamical systems.
In this paper, four distinct ideas are combined, which under a wide range of circumstances can give very rapidly converging series expansions for functional integrals. (1) Expansion of the functional being integrated in functional Taylor series. In the familiar case arising in quantum statistical mechanics, that of the Wiener integral of exp[−∫V(x(t))dt],V(x) being the perturbing potential, this is equivalent to expanding the characteristic functional of the probability functional of V(x(t)) in central moments of V(x(t)). The lowest-order term of the series is the approximation obtained by Feynman and Hibbs through a variational method. (2) Transfer of the harmonic term of the potential, when the functional integral is the quantum-statistical density matrix (Green's function of the Bloch equation), to the weighting function. This transforms the functional integral from a Wiener to an Uhlenbeck-Ornstein integral. The formal expressions for the terms of the expansion are somewhat more complicated, but they can be worked out, and the result is a great improvement in the speed of convergence of the series with decreasing temperature and/or decreasing relative magnitude of the anharmonic part of the potential. (3) ``Reservation of variables'' in the integration. This amounts to breaking the averaging process down into an average over subsets of the distributed random function (conditional average), followed by an averaging of these averages. Any step of this kind (it may be repeated within the subsets, etc.) gives an improvement of accuracy. (4) When the quantity being evaluated through functional integration is the partition function, the device introduced by Feynman and Hibbs, of interchanging the functional integration with the integration of the Green's function over the equated initial and final configuration-space points, may be combined with the above techniques. This eliminates one integration in the terms of the expansion and seems to improve accuracy at the same time. The general series obtained is correlated with more conventional operator techniques of quantum-mechanical perturbation theory, in order to answer the perennial question, does the path-integral method bring with it anything that could not be derived by other methods? It is in some sense a Feynman-Dyson expansion of the Green's function, but one that is further modified mathematically in a way characteristic only of the path-integral point of view, and which, moreover, improves its accuracy. It thus appears unlikely that the result is merely one of standard type disguised as a functional integral result. Sample numerical calculations are given to assay the accuracy of the methods, which are shown to compare very favorably with the traditional approximation of finite subdivision of the time interval.
The relation of theWigner function with the fair probability distribution called tomographic distribution or quantum tomogram associated with the quantum state is reviewed. The connection of the tomographic picture of quantum mechanics with the integral Radon transform of the Wigner quasidistribution is discussed. The Wigner–Moyal equation for the Wigner function is presented in the form of kinetic equation for the tomographic probability distribution both in quantum mechanics and in the classical limit of the Liouville equation. The calculation of moments of physical observables in terms of integrals with the state tomographic probability distributions is constructed having a standard form of averaging in the probability theory. New uncertainty relations for the position and momentum are written in terms of optical tomograms suitable for directexperimental check. Some recent experiments on checking the uncertainty relations including the entropic uncertainty relations are discussed.
An alternative approach to the quantum statistics of interacting particles is proposed. It consists of calculating the equilibrium thermodynamical quantities of the many-body system via the pair distribution function with the assumption that the particles interact with each other only through pair central forces. The proposed approach has some advantage over the usual treatment via the partition function in that the pair distribution function is easier to deal with than the partition function in certain circumstances particularly when the collective motion description of the system is desirable. This is because only the pair distribution function can be expressed directly in terms of the collective interaction which is closely connected with collective elementary excitation, such as a plasmon in the electron gas and a phonon in the hard-sphere Boson gas. The equation of state as well as the internal energy are obtained in the form of integrals of the pair distribution function. The close analogy between the pair distribution function and the two-body propagator, which appears in the quantum field theory, makes it possible to analyze the former by the use of Feynman diagrams identical with those usually introduced for the latter. The collective interaction, which is defined by the sum of the direct and the indirect interactions, is introduced as a particular partial sum of the perturbation series of the pair distribution function. This is used in rewriting the pair distribution function in terms of the collective interaction.It is shown that, while the simple chain approximation to the collective interaction in the electron gas is responsible for the transfer of a plasmon, the same approximation to the collective pseudo-interaction in the hard-sphere Boson system has a relation similar to that of transfer of a phonon, both cases occuring at low temperatures. The explicit calculation of the pair distribution functions for these systems at the absolute zero temperature is carried out up to the first order in the collective interaction (simple chain approximation.) These results are used to calculate the ground-state energies. For the electron gas the energy thus obtained confirms Gell-Mann-Bruckner's calculation of the correlation energy. For the hard-sphere Bosons the calculated energy reproduces the result of Lee, Huang, and Yang. The extension of the calculation to the finite temperature case is also indicated. In particular the classical Debye-Huckel equation of state for the electron gas is briefly discussed.
A formulation of quantum statistical mechanics is given, in terms of distribution functions. It is shown that all quantities of interest are obtained directly from nonlocal distribution functions ${\ensuremath{\gamma}}^{(1)}({{x}_{1}}^{\ensuremath{'}}, {x}_{1}, \ensuremath{\beta}), {\ensuremath{\gamma}}^{(2)}({{x}_{1}}^{\ensuremath{'}}, {{x}_{2}}^{\ensuremath{'}}, {x}_{1}{x}_{2}, \ensuremath{\beta}), \ensuremath{\cdots}.$ In a uniform system the Fourier transform of ${\ensuremath{\gamma}}^{(1)}({{x}_{1}}^{\ensuremath{'}}, {x}_{1}, \ensuremath{\beta})$ is the distribution of particles in k space, $n(k, \ensuremath{\beta})$. Various schemes for calculating these distribution functions directly are discussed. An approximate integral equation for $n(k, \ensuremath{\beta})$ is found, which can be solved by a converging iteration process. Some remarks are included on the application of the virial theorem.