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Physical Review Letters

1D Generalized Statistics Gas: A Gauge Theory Approach

Silvio Rabello

Published Dec 2, 1996• 14 citations
Publisher

Abstract

The gauge transformation shown in Eq. ( 12) in fact does not give a wave function obeying the free N-body Schrödinger equation as Eq. ( 13), in such a way that the "statistical" interaction cannot be removed.Nevertheless, this fact does not invalidate the main aim of the paper since the connection of this gauge theory with one-dimensional fermionic models has no relation to this.

DOI
10.1103/physrevlett.77.4851

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The gauge transformation shown in Eq. ( 12) in fact does not give a wave function obeying the free N-body Schrödinger equation as Eq. ( 13), in such a way that the "statistical" interaction cannot be removed.Nevertheless, this fact does not invalidate the main aim of the paper since the connection of this gauge theory with one-dimensional fermionic models has no relation to this.
A field theory with generalized statistics in one space dimension is introduced. The statistics enters the scene through the coupling of the matter fields to a statistical gauge field, as it happens in the Chern-Simons theory in two dimensions. We study the particle-hole excitations and show that the long wavelength physics of this model describes a gas obeying the Haldane generalized exclusion statistics. The statistical interaction is found to provide a way to describe the low-T critical properties of one-dimensional non-Fermi-liquids.
We show that the thermodynamic Bethe ansatz equations for one-dimensional integrable many-body systems can be reinterpreted in such a way that they only code the statistical interactions, in the sense of Haldane, between particles of identical or different momenta. Thus, the thermodynamic properties of these systems can be characterized by the generalized ideal gases recently proposed by one of us. For example, the Yang-Yang δδδ-function gas is a gas with specific statistical interactions between particles of different momenta, while the Calogero-Sutherland system provides a model for an ideal gas of particles with a fractional statistics.
The explicitly soluble Luttinger model is used as a basis for the description of the general interacting Fermi gas in one dimension, which will be called 'Luttinger liquid theory', by analogy with Fermi liquid theory. The excitation spectrum of the Luttinger model is described by density-wave, charge and current excitations; its spectral properties determine a characteristic parameter that controls the correlation function exponents. These relations are shown to survive in non-soluble generalisations of the model with a non-linear fermion dispersion. It is proposed that this low-energy structure is universal to a wide class of 1D systems with conducting or fluid properties, including spin chains.
We provide an extended account of the recent statistical mechanical theory of gauge invariance against operator shifting in quantum many-body systems [J. Müller and M. Schmidt, Phys. Rev. E 114, L022104 (2026)10.1103/dzz3-m28k]. The gauge transformation is enacted by a shifting superoperator that displaces the fundamental position and momentum degrees of freedom. The shifting superoperator constitutes a map between Hilbert space operators, and it features Lie algebra commutator structure. Averages of general observables remain invariant under the shifting both in and out of thermal equilibrium, as well as in ground states. The gauge invariance induces exact sum rules that interconnect global observables and associated locally resolved correlation functions. In particular we describe the resulting one-body force, hyperforce, product, and two-body sum rules. We relate the shifting superoperator to a previously formulated quantum canonical transformation and present the generalization of quantum shifting to multicomponent systems. The gauge theory respects fundamental fermionic and bosonic particle properties, as we demonstrate by proving the compatibility of operator shifting and exchange symmetry. We formulate the quantum version of hyperdensity functional theory to provide formal access to hyperforces as well as to general averaged quantum observables via universal density functionals. For time-dependent situations, we describe quantum dynamical gauge invariance and prove exact dynamical sum rules for nonequilibrium situations, as generated by Hamiltonian time dependence. We argue for the fundamental status of statistical mechanical gauge invariance based on the compliance of the underlying geometry with canonical quantization according to Dirac's correspondence principle. Analogies and differences of the quantum mechanical sum rules with their classical counterparts remain indicative of the respective levels of description.
The explicitly soluble Luttinger model is used as a basis for the description of the general interacting Fermi gas in one dimension, which will be called 'Luttinger liquid theory', by analogy with Fermi liquid theory. The excitation spectrum of the Luttinger model is described by density-wave, charge and current excitations; its spectral properties determine a characteristic parameter that controls the correlation function exponents. These relations are shown to survive in non-soluble generalisations of the model with a non-linear fermion dispersion. It is proposed that this low-energy structure is universal to a wide class of 1D systems with conducting or fluid properties, including spin chains.
Exact solutions of the Schrödinger equation describing a freely expanding Lieb-Liniger gas of delta-interacting bosons in one spatial dimension are constructed. We demonstrate that for any interaction strength the system enters a strongly correlated regime during such expansion. The asymptotic form of the wave function is shown to have the form characteristic for "impenetrable-core" bosons. Exact solutions are obtained by transforming a fully antisymmetric (fermionic) time-dependent wave function that obeys the Schrödinger equation for a free gas. This transformation employs a differential Fermi-Bose mapping operator that depends on the strength of the interaction and the number of particles.