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Springer eBooks

Many Body Perturbation Theory for Non-Uniform Electronic Systems

D. F. Scofield

Published Jan 1, 1974• 0 citations
Publisher
DOI
10.1007/978-1-4684-2820-9_8

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For uniform systems of spin-less fermions in d spatial dimensions with d > 1, interacting through the isotropic two-body potential v(r-r'), a celebrated theorem due to Luttinger (1961) states that under the_assumption_ of validity of the many-body perturbation theory the self-energy Sigma(k;epsilon), with 0 ,< epsilon_F, with alpha_k >,= 0. As this is, by definition, specific to self-energies of Landau Fermi-liquid systems, treatment of non-Fermi-liquid systems are therefore thought to lie outside the domain of applicability of the many-body perturbation theory; that, for these systems, the many-body perturbation theory should_necessarily_ break down. We demonstrate that Im[Sigma(k;epsilon)] ~ -,+ alpha_k (epsilon-epsilon_F)^2, epsilon >,< epsilon_F, is_implicit_ in Luttinger's proof and that, for d > 1, in principle nothing prohibits a non-Fermi-liquid-type (and, in particular Luttinger-liquid-type) Sigma(k;epsilon) from being obtained within the framework of the many-body perturbation theory. We in addition indicate how seemingly innocuous Taylor expansions of the self-energy with respect to k, epsilon or both amount to tacitly assuming that the metallic system under consideration is a Fermi liquid, whether the self-energy is calculated perturbatively or otherwise. Proofs that a certain metallic system is in a Fermi-liquid state, based on such expansions, are therefore tautologies.
Beyond the usual many body perturbation theory, with the eigenfunctional theory, we directly calculate the correlation function produced by the Coulomb interaction of electrons in the equation of one-electron Green function, and give the general expression of the non-local effective interaction potential in a Hartree-type potential, which is absent in all previous many body perturbation theories. This effective interaction potential originates from the quantum many body effect of the system, and it cannot be obtained directly by the usual perturbation expression approach. Moreover, using theoretical models, we demonstrate that this effective interaction potential can be used to characterize the electron correlation strength of the system.