Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

International Journal of Modern Physics B

Finite Temperature Many-Particle Theory of Condensed Matter Systems in the Functional Schrödinger Picture

Hyun Sik Noh, Sang Koo You, Chul Koo Kim

Published Jun 20, 1997• 6 citations
Publisher

Abstract

A finite temperature many-particle theory of condensed matter systems is formulated using the functional Schrödinger picture. Using the interacting electron gas as a model system, we solve the equation of motion for the density matrix variationally with a Gaussian type trial density matrix. We show that the present formalism yields the finite temperature Hartree–Fock results both for the para- and ferromagnetic states in a simple and convenient fashion. Implications of the present results and future prospects are also discussed.

DOI
10.1142/s0217979297000940

Related papers

Finite temperature many-particle theory of condensed matter systems in the functional Schroedinger picture

Hyun Sik Noh, Sang Koo You, Chul Koo Kim

A finite temperature many-particle theory of condensed matter systems is formulated using the functional Schroedinger picture. Using the interacting electron gas as a model system, we solve the equation of motion for the density matrix variationally with a Gaussian type trial density matrix. We show that the present formalism yields the finite temperature Hartree-Fock results both for the para- and ferromagnetic states in a simple and convenient fashion. Implications of the present results and future prospects are also discussed.

arXiv:cond-mat/9703101•Mar 11, 1997•0 citations

The Functional Schrödinger Picture Approach to Many-Particle Systems

Chul Koo Kim, Sang Koo You

A self-contained pedagogical introduction to the functional Schrödinger picture method of many-body theory is given at a level suitable for graduate students and also for many-body physicists who have not been exposed to the functional Schrödinger picture method previously. Mathematical tools necessary for the functional Schrödinger picture calculation are introduced. The method is first applied to various condensed matter problems including the electron gas, the Hubbard model, the BCS superconductivity, and dilute bose gas within the variational approximation. It is shown that the variational approximation with the Gaussian trial functional invariably leads into the Hartree-Fock results for both zero and finite temperature cases. In order to go beyond the Gaussian results, concepts of variational and optimized perturbation theories are introduced using simple quantum mechanical languages. Then, the variational perturbation theory in the functional Schrödinger picture is applied to the $λϕ^4$ model to yield the effective potential to the third order. The optimized perturbation theory is also applied to the $λϕ^4$ model to yield a general expression up to the second order.

arXiv:cond-mat/0212557•Dec 23, 2002•2 citations

Time-dependent functional Schrödinger picture approach to many-particle systems

Hyun Sik Noh, Mun Dae Kim, Chul Koo Kim +2 more

A time-dependent many-body theory for many-particle systems is formulated using the functional Schrödinger picture. Taking a Gaussian trial wave functional and using the variational principle, the equations of motion are obtained. The equations of motion are solved in the small oscillation regime to yield the generalized RPA results. The electron–hole excitation, the collective plasma oscillation for the paramagnetic state, the Stoner excitation and the spin wave for the ferromagnetic state are derived and discussed. As a further test on the versatility of the present method, the formalism is applied to the bound states of the exciton problem and shown to yield the governing equation in a straightforward manner.

Journal of Physics A Mathematical and General•Nov 13, 2001•1 citation

Functionals in many-particle physics

Richard M. Martin, Lucia Reining, David M. Ceperley

To avoid confusion, it is necessary to be quite explicit about what is assumed and what is to be proved. A. Klein, Phys. Rev. 121, 950 (1961) Summary The topic of this chapter is functionals that provide a concise formulation for thermodynamic quantities and Green's function methods in interacting many-body systems. Building upon the instructive examples of density functional theory and the Hartree– Fock approximation, functionals of the Green's function are developed to provide a framework for practical methods used extensively in many-body perturbation theory (Chs. 9–15), dynamical mean-field theory (Chs. 16–20), and their combination in Ch. 21. Functional concepts give a firm foundation for those methods, for example, they give the conditions for approximations to obey conservation laws. Additional background and specific aspects are in App. H. Many physical quantities can be expressed as functionals , i.e., they depend on an entire function.1 For example, in the quantum variational method to determine a wavefunction, the total energy of a system of many electrons is a functional of a many-body trial wavefunction ( r 1 , r 2 , …): it is the expectation value of the hamiltonian. At the variational minimum, assuming the trial wavefunction is completely flexible, one finds the many-body Schrödinger equation for the ground state. Many of the properties we are interested in are, formally, simple functionals of the ground- or excited-state wavefunctions. In the search for feasible ways to calculate properties such as excitation spectra, we are led to different types of functional. The idea is to deal only with a physical, measurable quantity Q of interest and a variational functional E [ Q ] of this quantity. The variational character of E allows one to derive equations that determine Q 0 , the value of Q for the system in a desired state, typically the ground state or equilibrium state at T ≠ 0. Other properties should be different functionals F m [ Q ] that can then be evaluated at Q = Q 0 . This strategy is outlined in Fig. 8.1. To appreciate the power of such approaches, one can consider the impact of density functional theory, which is formulated as a functional of the density n ( r ) of electrons; it is defined for a range of densities and the variational minimum for the energy functional E [ n ] leads to equations to determine the actual ground-state density n 0 ( r ) and total energy E 0 .

Cambridge University Press eBooks•May 31, 2016•0 citations

Bose quantum fluids at finite temperatures: A variational density-matrix approach

B. E. Clements, C. E. Campbell

The variational density-matrix approach introduced by Campbell, K\"urten, Ristig, and Senger [Phys. Rev. B 30, 3728 (1984)], to study finite-temperature Bose fluids is reformulated to avoid dealing directly with the entropy of the trial density matrix. We obtain exact expressions for the Euler-Lagrange equations for a finite-temperature trial statistical density matrix, which is the simplest finite-temperature generalization of a Jastrow trial ground-state wave function. A multicomponent hypernetted-chain method is developed to solve approximately these Euler-Lagrange equations at low temperatures. In leading order the results are shown to be equivalent to those obtained by Campbell et al. The current formalism provides a scheme to improve results of the previous approach.

Physical review. B, Condensed matter•Nov 1, 1992•6 citations

The Hartree–Fock approximation

Helmut Hofmann

Abstract This chapter formulates the Hartree-Fock approximation with density matrices, and discusses the properties of the Hartree-Fock equations together with the energy functional for the ground state energy. A generalization to finite thermal excitations is performed by applying the variational principle to the grand canonical ensemble. Finally, the equations for time-dependent Hartree-Fock (TDHF) are described both at zero and at finite temperature.

•Apr 17, 2008•0 citations
A finite temperature many-particle theory of condensed matter systems is formulated using the functional Schrödinger picture. Using the interacting electron gas as a model system, we solve the equation of motion for the density matrix variationally with a Gaussian type trial density matrix. We show that the present formalism yields the finite temperature Hartree–Fock results both for the para- and ferromagnetic states in a simple and convenient fashion. Implications of the present results and future prospects are also discussed.
A finite temperature many-particle theory of condensed matter systems is formulated using the functional Schroedinger picture. Using the interacting electron gas as a model system, we solve the equation of motion for the density matrix variationally with a Gaussian type trial density matrix. We show that the present formalism yields the finite temperature Hartree-Fock results both for the para- and ferromagnetic states in a simple and convenient fashion. Implications of the present results and future prospects are also discussed.
A self-contained pedagogical introduction to the functional Schrödinger picture method of many-body theory is given at a level suitable for graduate students and also for many-body physicists who have not been exposed to the functional Schrödinger picture method previously. Mathematical tools necessary for the functional Schrödinger picture calculation are introduced. The method is first applied to various condensed matter problems including the electron gas, the Hubbard model, the BCS superconductivity, and dilute bose gas within the variational approximation. It is shown that the variational approximation with the Gaussian trial functional invariably leads into the Hartree-Fock results for both zero and finite temperature cases. In order to go beyond the Gaussian results, concepts of variational and optimized perturbation theories are introduced using simple quantum mechanical languages. Then, the variational perturbation theory in the functional Schrödinger picture is applied to the λϕ4λϕ^4λϕ4 model to yield the effective potential to the third order. The optimized perturbation theory is also applied to the λϕ4λϕ^4λϕ4 model to yield a general expression up to the second order.
A time-dependent many-body theory for many-particle systems is formulated using the functional Schrödinger picture. Taking a Gaussian trial wave functional and using the variational principle, the equations of motion are obtained. The equations of motion are solved in the small oscillation regime to yield the generalized RPA results. The electron–hole excitation, the collective plasma oscillation for the paramagnetic state, the Stoner excitation and the spin wave for the ferromagnetic state are derived and discussed. As a further test on the versatility of the present method, the formalism is applied to the bound states of the exciton problem and shown to yield the governing equation in a straightforward manner.
To avoid confusion, it is necessary to be quite explicit about what is assumed and what is to be proved. A. Klein, Phys. Rev. 121, 950 (1961) Summary The topic of this chapter is functionals that provide a concise formulation for thermodynamic quantities and Green's function methods in interacting many-body systems. Building upon the instructive examples of density functional theory and the Hartree– Fock approximation, functionals of the Green's function are developed to provide a framework for practical methods used extensively in many-body perturbation theory (Chs. 9–15), dynamical mean-field theory (Chs. 16–20), and their combination in Ch. 21. Functional concepts give a firm foundation for those methods, for example, they give the conditions for approximations to obey conservation laws. Additional background and specific aspects are in App. H. Many physical quantities can be expressed as functionals , i.e., they depend on an entire function.1 For example, in the quantum variational method to determine a wavefunction, the total energy of a system of many electrons is a functional of a many-body trial wavefunction ( r 1 , r 2 , …): it is the expectation value of the hamiltonian. At the variational minimum, assuming the trial wavefunction is completely flexible, one finds the many-body Schrödinger equation for the ground state. Many of the properties we are interested in are, formally, simple functionals of the ground- or excited-state wavefunctions. In the search for feasible ways to calculate properties such as excitation spectra, we are led to different types of functional. The idea is to deal only with a physical, measurable quantity Q of interest and a variational functional E [ Q ] of this quantity. The variational character of E allows one to derive equations that determine Q 0 , the value of Q for the system in a desired state, typically the ground state or equilibrium state at T ≠ 0. Other properties should be different functionals F m [ Q ] that can then be evaluated at Q = Q 0 . This strategy is outlined in Fig. 8.1. To appreciate the power of such approaches, one can consider the impact of density functional theory, which is formulated as a functional of the density n ( r ) of electrons; it is defined for a range of densities and the variational minimum for the energy functional E [ n ] leads to equations to determine the actual ground-state density n 0 ( r ) and total energy E 0 .
The variational density-matrix approach introduced by Campbell, K\"urten, Ristig, and Senger [Phys. Rev. B 30, 3728 (1984)], to study finite-temperature Bose fluids is reformulated to avoid dealing directly with the entropy of the trial density matrix. We obtain exact expressions for the Euler-Lagrange equations for a finite-temperature trial statistical density matrix, which is the simplest finite-temperature generalization of a Jastrow trial ground-state wave function. A multicomponent hypernetted-chain method is developed to solve approximately these Euler-Lagrange equations at low temperatures. In leading order the results are shown to be equivalent to those obtained by Campbell et al. The current formalism provides a scheme to improve results of the previous approach.