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arXiv:2410.11537 · Physical review. B./Physical review. B

Spectral function of a bipolaron coupled to dispersive optical phonons

K. Kovač, J. Bonča

Published Mar 12, 2025• 2 citations
arXivHTMLPDF

Abstract

Using an efficient variational exact diagonalization method, we computed the electron removal spectral function within the framework of the Holstein-Hubbard model containing two electrons with opposite spins coupled to dispersive quantum optical phonons. We focus on how the interplay between the electron-phonon coupling and on-site Coulomb repulsion shapes the spectral function, a quantity directly relevant to angle-resolved photoemission spectroscopy (ARPES). Tuning the strengths of the electron-phonon coupling and the Hubbard interaction allows us to examine the evolution of the spectral properties of the system as it crosses over from a bound bipolaron to separate polarons. We find that phonon dispersion plays an important role: It substantially redistributes the spectral weight across the low- and the high-energy features and controls the emergence and the structure of distinct multiphonon continua. In regimes of strong electron-phonon coupling and low Coulomb repulsion, the spectral function exhibits a broad distribution reflecting bound bipolaronic states. Increasing the Coulomb repulsion weakens bipolaron binding, shifts the primary quasiparticle peak closer to polaronic behavior and confines the spectral weight near the Brillouin-zone center. Our results provide a framework for interpreting ARPES measurements in systems where phonon–mediated attraction competes with direct Coulomb repulsion.

DOI
10.1103/physrevb.111.115133

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Using an efficient variational exact diagonalization method, we computed the electron removal spectral function within the framework of the Holstein-Hubbard model containing two electrons with opposite spins coupled to dispersive quantum optical phonons. We focus on how the interplay between the electron-phonon coupling and on-site Coulomb repulsion shapes the spectral function, a quantity directly relevant to angle-resolved photoemission spectroscopy (ARPES). Tuning the strengths of the electron-phonon coupling and the Hubbard interaction allows us to examine the evolution of the spectral properties of the system as it crosses over from a bound bipolaron to separate polarons. We find that phonon dispersion plays an important role: It substantially redistributes the spectral weight across the low- and the high-energy features and controls the emergence and the structure of distinct multiphonon continua. In regimes of strong electron-phonon coupling and low Coulomb repulsion, the spectral function exhibits a broad distribution reflecting bound bipolaronic states. Increasing the Coulomb repulsion weakens bipolaron binding, shifts the primary quasiparticle peak closer to polaronic behavior and confines the spectral weight near the Brillouin-zone center. Our results provide a framework for interpreting ARPES measurements in systems where phonon–mediated attraction competes with direct Coulomb repulsion.
We investigate the ground-state properties of the bipolaron coupled to quantum dispersive optical phonons in the one-dimensional Holstein-Hubbard model. We concentrate on the interplay between the phonon dispersion and the Coulomb repulsion and their mutual effect on the bipolaron effective mass, the binding energy, and the phase diagram. Most surprisingly, the sign of the curvature of the optical phonon dispersion plays a decisive role in the bipolaron binding energy in the presence of the Coulomb repulsion UUU. In particular, when the sign of the phonon dispersion curvature matches the sign of the electron dispersion curvature, the bipolaron remains bound in the strong-coupling limit even when $U\ensuremath{\rightarrow}\ensuremath{\infty}$ and the binding emanates from the exchange of phonons between two electrons residing on adjacent sites. At moderate electron-phonon coupling a light bipolaron exists up to large values of UUU. Finally, an intuitive explanation of the role of the phonon dispersion on the bipolaron binding energy is derived using the strong-coupling limit where the binding emanates from the exchange of phonons between two electrons residing on adjacent sites which leads to enhanced stability of bipolarons at elevated Coulomb repulsion.
We explore the ground state and thermodynamic properties of the polaron coupled to quantum dispersive optical phonons in one spatial dimension. Calculations are performed using the finite--temperature Lanczos method augmented by a highly efficient construction of the variational Hilbert space. We focus on the electron removal spectral function as relevant for the angle-resolved photoemission experiments. We show that photoemission spectroscopy can be used to measure the phonon dispersion relation in a dilute system of polarons. The spectral weight of observed phonon bands is proportional to the phonon contribution to the wavefunction at finite phonon momentum. In addition, we demonstrate that when removing an electron from a polaron ground state, the polaron band does not appear in the spectral function. The latter becomes observable only at elevated temperatures.
We study static and dynamic properties of an electron coupled to dispersive quantum optical phonons in the framework of the Holstein model defined on a one-dimensional lattice. Calculations are performed using the Lanczos algorithm based on a highly efficient construction of the variational Hilbert space. Even small phonon dispersion has a profound effect on the low-energy optical response. While the upward phonon dispersion broadens the optical spectra due to single-phonon excitations, the downward dispersion has the opposite effect. With increasing dispersion, a multiphonon excitation (MPE) state becomes the lowest excited state of the system at zero momentum and determines the low-frequency response of the optical conductivity where the threshold for optical absorption moves below the single-phonon frequency. Multiphonon states form a well-defined bandlike feature just above the polaron band as clearly seen in the electron spectral function. Low-energy MPEs should be observable in systems with strong optical phonon dispersion in optical as well as angle-resolved photoemission experiments.
We use density matrix renormalization group (DMRG) and variational exact diagonalization (VED) to calculate the single-electron removal spectral weight for the Hubbard-Holstein model at low electron densities. Tuning the strength of the electron-phonon coupling and of the Hubbard repulsion allows us to contrast the results for a liquid of polarons versus a liquid of bipolarons. The former shows spectral weight up to the Fermi energy, as expected for a metal. The latter has a gap in its spectral weight, set by the bipolaron binding energy, although this is also a (strongly correlated) metal. This difference suggests that angle-resolved photoemission spectroscopy could be used to identify liquids of pre-formed pairs. Furthermore, we show that the one-dimensional liquid of incoherent bipolarons is well approximated by a "Bose sea" of bosons that are hard-core in momentum space, occupying the momenta inside the Fermi sea but otherwise noninteracting. This new proposal for a strongly correlated many-body wave function opens the way for studying various other properties of incoherent (nonsuperconducting) liquids of preformed pairs in any dimension.
This thesis first reviews and examines the Angle Resolved Photoemission Spectroscopy (ARPES) experiment. It is shown that the spectral density function, familiar from the Green's function method of studying correlated systems, can be directly measured. A model spectral function with a nontrivial self-energy is then used to test an improvement to a recently arrived method[15,17] to analyze ARPES data. This new method relies on self-consistency between the real and imaginary parts of the self-energy (as measured through the Kramers-Kronig transform) to overcome the requirement of knowing the bare electronic structure. Through this, the method extracts both the complex self-energy and the bare electronic structure from the spectral function. The method described here is an improvement on this idea as previously implemented in that a strict form for the bare band dispersion (previously considered linear or quadratic) is never assumed. Although the method here utilized a polynomial of arbitrary degree, it could be trivially expanded to use any other functional form so long as both the value and first derivative are known analytically as a function of the fitting parameters. Using Mona Berciu's first order momentum average (MA) approximation[2] as implemented by Glen Goodvin[8] the spectral function as well as momentum independent self-energy were calculated for the Holstein polaron for a wide range of parameters. It was found that self-consistent spectral function analysis was highly successful at extracting the self energy and bare electronic dispersion from the spectral function over a consistent subset of these parameters. For studies outside this range of parameters the more traditional ARPES analysis method of measuring renormalization is also examined.
We have computed static and dynamic properties of an electron coupled to hard-core-boson (HCB) degrees of freedom in one spatial dimension. The polaron, an electron dressed with HCB excitations, remains light even in the strong-coupling limit as its effective mass remains of the order of the free-electron mass. This result is in a sharp contrast to the Holstein model where the electron effective mass increases exponentially with the electron-phonon coupling. HCB degrees of freedom mediate the attractive potential between two electrons that form a bound singlet bipolaron state at any nonzero coupling strength. In the low-frequency regime of the electron spectral function we observe a quasiparticle (QP) band that is separated from the continuum of states only in the central part of the Brillouin zone. The quasiparticle weight approaches zero as the QP band enters the continuum where it obtains a finite lifetime. At finite temperature an electron can annihilate thermally excited HCBs. Such thermally activated processes lead to a buildup of the spectral weight below the QP band. While the investigated model bears a resemblance with the Holstein model, we point out many important differences that originate from the binary HCB excitation spectrum, which in turn mimics spin-12\frac{1}{2}21​ degrees of freedom.