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Journal of Physics Conference Series

Transient spectra of photo-excited states in double exchange model

Yu Kanamori, Hiroaki Matsueda, Sumio Ishihara

Published Feb 1, 2009• 0 citations
Publisher

Abstract

We investigate photo-induced effect in strongly correlated electron systems where conduction electrons couple with localized spins. In particular, the photo-induced phenomena in a charge-ordered insulator associated with antiferromagnetic order are examined. Transient excitation spectra are calculated by the exact diagonalization method in one-dimensional extended double exchange model. We find that in the photo-excited states, finite spectral weights in the one-particle excitation spectra appear inside the insulating gap and its band width increases with increasing time. This change of the electronic structure is correlated with the time development of the localized spin correlation. These results indicate that a strong coupling between spin and charge governs the photo-induced phenomena in this system.

DOI
10.1088/1742-6596/148/1/012060

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We investigate photo-induced effect in strongly correlated electron systems where conduction electrons couple with localized spins. In particular, the photo-induced phenomena in a charge-ordered insulator associated with antiferromagnetic order are examined. Transient excitation spectra are calculated by the exact diagonalization method in one-dimensional extended double exchange model. We find that in the photo-excited states, finite spectral weights in the one-particle excitation spectra appear inside the insulating gap and its band width increases with increasing time. This change of the electronic structure is correlated with the time development of the localized spin correlation. These results indicate that a strong coupling between spin and charge governs the photo-induced phenomena in this system.
Photoinduced spin and charge dynamics in double-exchange model are numerically studied. The Lanczos method and the density-matrix renormalization-group method are applied to one-dimensional finite-size clusters. By photon irradiation in a charge-ordered (CO) insulator associated with antiferromagnetic (AFM) correlation, both the CO and AFM correlations collapse rapidly, and appearances of new peaks inside of an insulating gap are observed in the optical spectra and the one-particle excitation spectra. Time evolutions of the spin correlation and the in-gap state are correlated with each other, and are governed by the transfer integral of conduction electrons. Results are interpreted by the charge kink/antikink picture and their effective motions which depend on the localized spin correlation. Pump-photon density dependence of spin and charge dynamics are also studied. Roles of spin degree of freedom are remarkable in a case of weak photon density. Implications of the numerical results for the pump-probe experiments in perovskite manganites are discussed.
We study photoinduced optical responses of one-dimensional strongly correlated electron systems. The optical conductivity spectra are calculated for the ground state and a photoexcited state in the one-dimensional Hubbard model at half filling by using the exact diagonalization method. It is found that, in the Mott insulator phase, the photoexcited state has large spectral weights including the Drude weight below the optical gap. As a consequence, the spectral weight above the optical gap is largely reduced. These results imply that a metallic state is induced by photoexcitation. Comparison between the photoexcited and hole-doped states shows that the photoexcitation is similar to chemical doping.
We theoretically investigate the transient spectral function during the photoinduced melting of charge order in a correlated electron system, to unravel the dynamical processes triggered by different initial excitations. We employ a one-dimensional interacting spinless fermion model introducing a pulsed laser light, and perform a comparative study by the Hartree-Fock approximation and by the exact diagonalization method to numerically solve the time-dependent Schrödinger equation. We find characteristic behavior in the transient spectral function, whose features strongly depend on the pump light frequency ωpω_pωp​. When ωpω_pωp​ is resonant with the collective phase mode of frequency Ωc≃ΔCO/2Ω_c\simeq Δ_{\rm CO}/2Ωc​≃ΔCO​/2, where ΔCOΔ_{\rm CO}ΔCO​ is the charge gap, the transient spectral function exhibits a photoinduced in-gap weight which triggers large responses. With increasing the laser intensity, the development of in-gap weight directly turns into the collapse of the gap. This charge-order destabilization process is in sharp contrast to the case of ωp>ΔCOω_p>Δ_{\rm CO}ωp​>ΔCO​, where the photoirradiation induces interband electron-hole excitations giving rise to a shrinkage of the gap. The impact of quantum fluctuations and spatial inhomogeneity on the photoinduced dynamics is also discussed.
We theoretically study photoemission spectra for photodoped one-dimensional Mott insulators that can host excitons, and show that their spectral characteristics differ qualitatively from those of photodoped semiconductors. In conventional semiconductors, photoemission spectra are well understood; free charge carriers generate spectral weight near the bottom of the conduction band, while the formation of excitons leads to replica features of the valence band appearing inside the band gap. In one-dimensional Mott insulators, on the other hand, strong correlations give rise to fractionalized elementary excitations-spinons, holons, and doublons-which fundamentally modify the photoemission response. We find that when photodoped carriers, i.e., doublons and holons, remain unbound, the photoemission spectrum directly reflects the dispersion of spinons, i.e., magnetic elementary excitations. In contrast, when a doublon and a holon form an excitonic bound state, replica structures of the lower Hubbard band emerge inside the Mott gap, carrying contributions from both spinon and holon excitations. Importantly, the distribution of the in-gap signal depends sensitively on the degree of doublon-holon binding. The origin of these spectral features is clarified through a combination of exact diagonalization and the slave-particle approach. These results indicate that photoemission from photoinduced carriers and excitons in strongly correlated electron systems can provide information on magnetic properties and carrier-binding properties.
The effective Hamiltonian of the Hubbard model for multiphoton excited states is derived assuming a strong Coulomb repulsion. Diagonalizing the effective Hamiltonian exactly, the lowest energy one-photon excited state is calculated in the two-dimensional Hubbard model at half-filling, and its physical properties are investigated. For t/U< 0.0165,t/U<~0.0165,t/U< 0.0165, where t is the magnitude of the transfer integral between the nearest-neighbor sites and U is an on-site Coulomb repulsion energy, ferromagnetic spin order is photogenerated from the antiferromagnetic ground state, and, for t/U> 0.0166,t/U>~0.0166,t/U> 0.0166, antiferromagnetic spin order survives one-photon excitation. Photoinjected opposite charges are unbound because of strong electron correlation for t/U< 0.08,t/U<~0.08,t/U< 0.08, and bound for t/U> 0.08.t/U>~0.08.t/U> 0.08. The probability that the photoinjected opposite charges are on nearest-neighbor sites is strongly suppressed through all the correlation regions including this charge-bound region. We see a tendency toward spin-charge separation, but the coupling is not small in the one-photon excited state. The local spin structure around the bound positive and negative charges injected by photoexcitation is quite different from that induced by two-hole doping; this result suggests that multiphoton excitation will generate an electronic order which differs from that generated by doping.
The study of nonequilibrium phenomena in interacting lattice systems can provide new perspectives on correlation effects, and information on metastable states of matter. Mott insulators are a promising class of systems for nonequilibrium studies, since they exhibit exotic phenomena and complex phase diagrams upon doping, and because a large Mott gap provides protection against fast thermalization and heating after photo-excitations. We can thus expect the emergence of interesting transient states and photo-induced phases in Mott systems. This review presents the current understanding of the mechanisms which control the time evolution of photo-doped charge carriers and the properties of photo-induced metastable states. We focus on recent theoretical progress, identify the relevant underlying concepts, and link them to experimental observations. The review starts with a general discussion of field-induced nonequilibrium setups and an overview of key experiments which revealed characteristic properties of photo-excited Mott states, proceeds with a compact overview of the theoretical tools which have been developed to investigate these strongly correlated nonequilibrium states, and then analyzes Mott insulators driven out of equilibrium by static electric fields, periodic fields, and short laser pulses. We also discuss the appearance of nonthermal electronic orders in photo-excited Mott systems, including nonthermal spin and orbital orders, ηηη pairing states, and novel types of excitonic orders.