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Journal of Mathematical Physics

Quantum virial coefficients as cumulants of imaginary time-ordered Mayer diagrams

Antoine Royer

Published Apr 1, 1983• 5 citations
Publisher

Abstract

The virial coefficients for a quantum gas (including quantum statistics) are expressed as sums of cumulants of connected (generalized) Mayer diagrams, the cumulants being built on the irreducible blocks of the diagrams. The Mayer diagrams are defined for the quantum case in terms of imaginary time-ordered exponentials, the quantum statistics being incorporated in the guise of multiparticle interactions. In order to extend Mayer diagrams to multiparticle interactions, we utilize terminology and methods from the theory of hypergraphs. The virial coefficients naturally separate into a quantum Boltzmann gas contribution, an ideal quantum gas contribution, and a final term expressing correlations between dynamics and statistics. In the classical limit, connected Mayer diagrams factorize into their irreducible blocks; the cumulants over irreducible blocks then vanish (by a basic property of cumulants), except for diagrams which are themselves irreducible, whence the classical result of Mayer (extended to multiparticle interactions). In the quantum case, the imaginary time ordering prevents the factorization into irreducible blocks by time entangling them. As a further illustration of the use of hypergraph-cumulant methods, we directly deduce the expressions of the virial coefficients in terms of Ursell–Kahn–Uhlenbeck cluster functions (the ideal quantum gas contribution naturally appears in that form).

DOI
10.1063/1.525779

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The virial coefficients for a quantum gas (including quantum statistics) are expressed as sums of cumulants of connected (generalized) Mayer diagrams, the cumulants being built on the irreducible blocks of the diagrams. The Mayer diagrams are defined for the quantum case in terms of imaginary time-ordered exponentials, the quantum statistics being incorporated in the guise of multiparticle interactions. In order to extend Mayer diagrams to multiparticle interactions, we utilize terminology and methods from the theory of hypergraphs. The virial coefficients naturally separate into a quantum Boltzmann gas contribution, an ideal quantum gas contribution, and a final term expressing correlations between dynamics and statistics. In the classical limit, connected Mayer diagrams factorize into their irreducible blocks; the cumulants over irreducible blocks then vanish (by a basic property of cumulants), except for diagrams which are themselves irreducible, whence the classical result of Mayer (extended to multiparticle interactions). In the quantum case, the imaginary time ordering prevents the factorization into irreducible blocks by time entangling them. As a further illustration of the use of hypergraph-cumulant methods, we directly deduce the expressions of the virial coefficients in terms of Ursell–Kahn–Uhlenbeck cluster functions (the ideal quantum gas contribution naturally appears in that form).
A systematic generalization of the Mayer cluster integral theory has been developed to deal with the quantum statistics of interacting particles. The grand partition function appears in a natural way and the cluster integrals are integrals over propagators which are derived from the Green's function solution of the Bloch equation (which follows from the Schroedinger equation by replacing it/ℏ by β = 1/kT). Every cluster integral can be represented by a hybrid of a Mayer graph and a Feynman diagram in (β, r) space. The generalization of classical ring cluster integrals has been analyzed. It is shown that in the case of the electron gas the classical limit of the contribution of these integrals to the grand partition function yields the Debye-Huckel theory while the low temperature limit leads to the Gell-Mann—Brueckner equation for the correlation energy of the ground state. A prescription is given for the construction of the cluster integral associated with any given diagram.
A general method of calculation is described for quantum statistical mechanics. It is based on a simplification of the Laplace transform of the density matrix which follows from a theorem due to Hugenholtz. The basic result is that an element of the density matrix can be written as a sum over graphs, with the contribution of each graph factored into contributions from connected or linked graphs. Applied to the grand partition function, the exponential formula of Bloch and DeDominicis is obtained in a simple way. A similar formula is then derived for the canonical ensemble for the case of a nondegenerate gas. In this way the familiar result of Uhlenbeck and Beth is obtained for the second virial coefficient. Techniques are also introduced for evaluating ensemble averages of operators. In this connection, some care must be exercised in the case of diagonal operators. Finally, these methods are used to calculate the pair-correlation function for a system of fermions interacting through short-range forces.
The virial expansion characterizes the high-temperature approach to the quantum-classical crossover in any quantum many-body system. Here, we calculate the virial coefficients up to the fifth order of Fermi gases in one, two, and three dimensions, with attractive contact interactions, as relevant for a variety of applications in atomic and nuclear physics. To that end, we discretize the imaginary-time direction and calculate the relevant canonical partition functions. In coarse discretizations, we obtain analytic results featuring relationships between the interaction-induced changes $\mathrm{\ensuremath{\Delta}}{b}_{3}, \mathrm{\ensuremath{\Delta}}{b}_{4}$, and $\mathrm{\ensuremath{\Delta}}{b}_{5}$ as functions of $\mathrm{\ensuremath{\Delta}}{b}_{2}$, the latter being exactly known in many cases by virtue of the Beth-Uhlenbeck formula. Using automated-algebra methods, we push our calculations to progressively finer discretizations and extrapolate to the continuous-time limit. We find excellent agreement for $\mathrm{\ensuremath{\Delta}}{b}_{3}$ with previous calculations in all dimensions and we formulate predictions for $\mathrm{\ensuremath{\Delta}}{b}_{4}$ and $\mathrm{\ensuremath{\Delta}}{b}_{5}$ in one and two dimensions. We also provide, for a range of couplings, the subspace contributions $\mathrm{\ensuremath{\Delta}}{b}_{31}, \mathrm{\ensuremath{\Delta}}{b}_{22}, \mathrm{\ensuremath{\Delta}}{b}_{41}$, and $\mathrm{\ensuremath{\Delta}}{b}_{32}$, which determine the equation of state and static response of polarized systems at high temperature. As a performance check, we compare the density equation of state and Tan contact with quantum Monte Carlo calculations, diagrammatic approaches, and experimental data where available. Finally, we apply Pad\'e and Pad\'e-Borel resummation methods to extend the usefulness of the virial coefficients to approach and in some cases go beyond the unit-fugacity point.
In the framework of real-time Green's functions, the general kinetic equations are investigated in a first-order gradient expansion. Within this approximation, the problem of the reconstruction of the two-time correlation functions from the one-time Wigner function was solved. For the Wigner function, a cluster expansion is found in terms of a quasiparticle distribution function. In equilibrium, this expansion leads to the well-known generalized Beth-Uhlenbeck expression of the second virial coefficient. As a special case, the T-matrix approximation for the self-energy is investigated. The quantum kinetic equation derived thus has, besides the (Markovian) Boltzmann collision integral, additional terms due to the retardation expansion which reflect memory effects. Special interest is paid to the case that bound states exist in the system. It is shown that the bound state contribution, which can be introduced via a bilinear expansion of the two-particle T matrix, follows from the first-order retardation term in the general kinetic equation. The full Wigner function is now a sum of one function describing the unbound particles and another one for the bound state contribution. The latter two functions have to be determined from a coupled set of kinetic equations. In contrast to the quantum Boltzmann equation, energy and density of a nonideal system are conserved. \textcopyright{} 1996 The American Physical Society.
The Beth Uhlenbeck formula gives an exact (quantum) expression of the second virial correction to the equation of state of a (slightly degenerate) dilute gas. We show how this result can be extended to arbitrary degeneracy provided that the interaction potential has a sufficiently short range. For this purpose we develop a formalism based on the use of Ursell operators, which contain no symmetrization in themselves (they correspond to an auxiliary system of distinguishable particles) and we show how they can be used for a system of identical particles. A concise expression generalizing the Beth Uhlenbeck formula is obtained, which is equally valid for bosons and fermions Higher order corrections are also introduced. The formalism is rather general and will be applied to other cases in forthcoming articles.