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arXiv:1708.08696 · Physical Review A

High-accuracy energy formulas for the attractive two-site Bose-Hubbard model

Igor Ermakov, Tim Byrnes, N. M. Bogoliubov

Published Feb 20, 2018• 2 citations
arXivHTMLPDF

Abstract

The attractive two-site Bose-Hubbard model is studied within the framework of the analytical solution obtained by the application of the quantum inverse scattering method. The structure of the ground and excited states is analyzed in terms of solutions of Bethe equations, and an approximate solution for the Bethe roots is given. This yields approximate formulas for the ground-state energy and for the first excited-state energy. The obtained formulas work with remarkable precision for a wide range of parameters of the model, and are confirmed numerically. An expansion of the Bethe state vectors into a Fock space is also provided for evaluation of expectation values, although this does not have accuracy similar to that of the energies.

DOI
10.1103/physreva.97.023626

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The attractive two-site Bose-Hubbard model is studied within the framework of the analytical solution obtained by the application of the quantum inverse scattering method. The structure of the ground and excited states is analyzed in terms of solutions of Bethe equations, and an approximate solution for the Bethe roots is given. This yields approximate formulas for the ground-state energy and for the first excited-state energy. The obtained formulas work with remarkable precision for a wide range of parameters of the model, and are confirmed numerically. An expansion of the Bethe state vectors into a Fock space is also provided for evaluation of expectation values, although this does not have accuracy similar to that of the energies.
Exactly solvable models provide a unique method, via qualitative changes in the distribution of the ground-state roots of the Bethe ansatz equations, to identify quantum phase transitions. Here we expand on this approach, in a quantitative manner, for two models of Bose–Einstein condensates. The first model deals with the interconversion of bosonic atoms and molecules. The second is the two-site Bose–Hubbard model, widely used to describe tunneling phenomena in Bose–Einstein condensates. For these systems we calculate the ground-state root density. This facilitates the determination of analytic forms for the ground-state energy, and associated correlation functions through the Hellmann–Feynman theorem. These calculations provide a clear identification of the quantum phase transition in each model. For the first model we obtain an expression for the molecular fraction expectation value. For the two-site Bose–Hubbard model we find that there is a simple characterization of condensate fragmentation.
The extended Bose-Hubbard model for a double-well potential with atom-pair tunneling is studied. Starting with a classical analysis we determine the existence of three quantum phases: self-trapping, phase-locking, and Josephson states. From this analysis we build the parameter space of quantum phase transitions between degenerate and nondegenerate ground states driven by the atom-pair tunneling. Considering only the repulsive case, we confirm the phase transition by the measure of the energy gap between the ground state and the first excited state. We study the structure of the solutions of the Bethe ansatz equations for a small number of atoms. An inspection of the roots for the ground state suggests a relationship to the physical properties of the system. By studying the energy gap we find that the profile of the roots of the Bethe ansatz equations is related to a quantum phase transition.
The energy gap between the ground state and the first excited state of the one-dimensional attractive Bose-Hubbard Hamiltonian is investigated in connection with directed polymers in random media. The excitation gap Δis obtained by exact diagonalization of the Hamiltonian in the two- and three-particle sectors and also by an exact Bethe Ansatz solution in the two-particle sector. The dynamic exponent z is found to be 2. However, in the intermediate range of the size L where UL~O(1), U being the attractive interaction, the effective dynamic exponent shows an anomalous peak reaching high values of 2.4 and 2.7 for the two- and the three-particle sectors, respectively. The anomalous behavior is related to a change in the sign of the first excited-state energy. In the two-particle sector, we use the Bethe Ansatz solution to obtain the effective dynamic exponent as a function of the scaling variable UL/π. The continuum version, the attractive delta-function Bose-gas Hamiltonian, is integrable by the Bethe Ansatz with suitable quantum numbers, the distributions of which are not known in general. Quantum numbers are proposed for the first excited state and are confirmed numerically for an arbitrary number of particles.
We employ an exact Bethe ansatz solution to study the repulsive Bose–Hubbard dimer model. Using a continuum approximation we solve for the ground state root density and in turn compute the ground state energy per particle. The formula so obtained is accurate for a finite-sized system in the weak coupling limit. Surprisingly, the formula diverges from the numerically calculated value as the number of particles increases. This indicates that the formula fails to predict the ground state energy per particle in the thermodynamic limit.
The ground-state energy and energy gap to the first excited state are calculated for the attractive Hubbard model in one dimension using both the Bethe ansatz equations and the variational BCS wave function. Comparisons are provided as a function of coupling strength and electron density. While the ground-state energies are always in very good agreement, the BCS energy gap is sometimes incorrect by an order of magnitude, particularly at half-filling. Finite-size effects are also briefly discussed for cases where an exact solution in the thermodynamic limit is not possible. In general, the BCS result for the energy gap is poor compared to the exact result.
Ground-state properties of the attractive Hubbard model in one dimension are studied by means of both the exact Bethe-ansatz formalism and the self-consistent field (SCF) approach with renormalized chemical potential for general band fillings n and a wide range of coupling strength U/t.U/t.U/t. The energy, the concentration of double occupied sites, the kinetic energy and the chemical potential of the ground state are in a good numerical agreement with the exact results over a wide range of parameters U/tU/tU/t and n. The concentration of local pairs or double occupied sites in the Bethe-ansatz solution serves as a suitable parameter measuring the electron pairing correlations. The SCF theory provides a simple analytical relationship between the concentration of double occupied sites, the band filling and the BCS order parameter, valid for arbitrary U/tU/tU/t and n. The calculated energy gap, the BCS order parameter, the phase diagram and the compressibility are also discussed. The SCF theory in one dimension distinguishes the order parameter from the excitation gap and suggests a smooth crossover away from half-filling (at $n\ensuremath{\ne}1)$ from the BCS pairing to the Bose condensation regime under the variation of U/tU/tU/t and n.