arXiv subjects

Kenji Yonemitsu

Publications and source records attributed to Kenji Yonemitsu.

At least 55 records · Page 3Linked to original sources

arXiv2008

Enhanced coherent dynamics near a transition between neutral quantum-paraelectric and ionic ferroelectric phases in the quantum Blume-Emery-Griffiths model

Nonequilibrium dynamics are studied near the quantum phase transition point in the one-dimensional quantum Blume-Emery-Griffiths model. Its pseudo-spin component $ S^z $ represents an electric polarization, and $ (S^z)^2 $ corresponds to ionicity, in mixed-stack charge-transfer complexes that exhibit a transition between neutral quantum-paraelectric and ionic ferroelectric (or antiferroelectric) phases. The time-dependent Schrödinger equation is solved for the exact many-body wave function in the quantum paraelectric phase. After impact force is introduced on a polarization locally in space and time, polarizations and ionicity coherently oscillate. The oscillation amplitudes are large near the quantum phase transition point. The energy supplied by the impact flows linearly into these oscillations, so that the nonequilibrium behavior is uncooperative.

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arXiv2008

Polaronic states with Spin-Charge-Coupled Excitation in a 1D Mott Insulator K-TCNQ

We discuss photogenerated midgap states of a one-dimensional (1D) dimerized Mott insulator, potassium-tetracyanoquinodimethane (K-TCNQ). Two types of phonon modes are taken into account: intermolecular and intramolecular vibrations. We treat these phonon modes adiabatically and analyze a theoretical model by using the density-matrix renormalization group (DMRG). Our numerical results demonstrate that the intermolecular lattice distortion is necessary to reproduce the photoinduced midgap absorption in K-TCNQ. We find two types of midgap states. One is a usual polaronic state characterized by a localized elementary excitation. The other is superposition of two types of excitations, a doped-carrier state and a triplet-dimer state, which can be generally observed in 1D dimerized Mott insulators, not limited to K-TCNQ.

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arXiv2008

Charge Order with Structural Distortion in Organic Conductors: Comparison between θ-(ET)2RbZn(SCN)4 and α-(ET)2I3

Charge ordering with structural distortion in quasi-two-dimensional organic conductors θ-(ET)2RbZn(SCN)4 (ET=BEDT-TTF) and α-(ET)2I3 is investigated theoretically. By using the Hartree-Fock approximation for an extended Hubbard model which includes both on-site and intersite Coulomb interactions together with Peierls-type electron-lattice couplings, we examine the role of lattice degrees of freedom on charge order. It is found that the experimentally observed, horizontal charge order is stabilized by lattice distortion in both compounds. In particular, the lattice effect is crucial to the realization of the charge order in θ-(ET)2RbZn(SCN)4, while the peculiar band structure whose symmetry is lower than that of θ-(ET)2RbZn(SCN)4 in the metallic phase is also an important factor in α-(ET)2I3 together with the lattice distortion. For α-(ET)2I3, we obtain a phase transition from a charge-disproportionated metallic phase to the horizontal charge order with lattice modulations, which is consistent with the latest X-ray experimental result.

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arXiv2007

Suppression of rectification at metal-Mott-insulator interfaces

Charge transport through metal-Mott-insulator interfaces is studied and compared with that through metal-band-insulator interfaces. For band insulators, rectification has been known to occur owing to a Schottky barrier, which is produced by the work-function difference. For Mott insulators, however, qualitatively different current-voltage characteristics are obtained. Theoretically, we use the one-dimensional Hubbard model for a Mott insulator and attach to it the tight-binding model for metallic electrodes. A Schottky barrier is introduced by a solution to the Poisson equation with a simplified density-potential relation. The current density is calculated by solving the time-dependent Schrödinger equation. We mainly use the time-dependent Hartree-Fock approximation, and also use exact many-electron wave functions on small systems for comparison. Rectification is found to be strongly suppressed even for large work-function differences. We show its close relationship with the fact that field-effect injections into one-dimensional Mott insulators are ambipolar. Experimentally, we fabricated asymmetric contacts on top of single crystals of quasi-one-dimensional organic Mott and band insulators. Rectification is strongly suppressed at an interface between metallic magnesium and Mott-insulating (BEDT-TTF)(F$_2$TCNQ) [BEDT-TTF=bis(ethylenedithio)tetrathiafulvalene, F$_2$TCNQ=2,5-difluorotetracyanoquinodimethane].

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arXiv2007

Mechanism of Ambipolar Field-Effect Transistors on One-Dimensional Organic Mott Insulators

The experimentally observed, ambipolar field-effect characteristics of Mott insulators are reproduced in the one-dimensional Hubbard model attached to a tight-binding model for source and drain electrodes. The formation of Schottky barriers, originating from the work-function difference, is taken into account by a potential satisfying the Poisson equation with an appropriate boundary condition. Then, these field-effect characteristics are shown to be related by unique current-voltage characteristics of metal-Mott-insulator interfaces.

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arXiv2007

Photoinduced melting of charge order in a quarter-filled electron system coupled with different types of phonons

Photoinduced melting of charge order is calculated by using the exact many-electron wave function coupled with classically treated phonons in the one-dimensional quarter-filled Hubbard model with Peierls and Holstein types of electron-phonon couplings. The model parameters are taken from recent experiments on (EDO-TTF)_2PF_6 (EDO-TTF=ethylenedioxy-tetrathiafulvalene) with (0110) charge order, where transfer integrals are modulated by molecular displacements (bond-coupled phonons) and site energies by molecular deformations (charge-coupled phonons). The charge-transfer photoexcitation from (0110) to (0200) configurations and that from (0110) to (1010) configurations have different energies. The corresponding excited states have different shapes of adiabatic potentials as a function of these two phonon amplitudes. The adiabatic potentials are shown to be useful in understanding differences in the photoinduced charge dynamics and the efficiency of melting, which depend not only on the excitation energy but also on the relative phonon frequency of the bond- and charge-coupled phonons.

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arXiv2007

Effects of Electron-Lattice Coupling on Charge Order in θ-(ET)2X

Charge ordering accompanied by lattice distortion in quasi-two dimensional organic conductors θ-(ET)2X (ET=BEDT-TTF) is studied by using an extended Hubbard model with Peierls-type electron-lattice couplings within the Hartree-Fock approximation. It is found that the horizontal-stripe charge-ordered state, which is experimentally observed in θ-(ET)2RbZn(SCN)4, is stabilized by the self-consistently determined lattice distortion. Furthermore, in the presence of the anisotropy in nearest-neighbor Coulomb interactions Vij, the horizontal charge order becomes more stable than any other charge patterns such as diagonal, vertical and 3-fold-type states. At finite temperatures, we compare the free energies of various charge-ordered states and find a first-order transition from a metallic state with 3-fold charge order to the insulating state with the horizontal charge order. The role of lattice degrees of freedom in the realization of the horizontal charge order and the relevance to experiments on θ-(ET)2X are discussed.

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arXiv2007

Charge-Transfer Excitations in One-Dimensional Dimerized Mott Insulators

We investigate the optical properties of one-dimensional (1D) dimerized Mott insulators using the 1D dimerized extended Hubbard model. Numerical calculations and a perturbative analysis from the decoupled-dimer limit clarify that there are three relevant classes of charge-transfer (CT) states generated by photoexcitation: interdimer CT unbound states, interdimer CT exciton states, and intradimer CT exciton states. This classification is applied to understanding the optical properties of an organic molecular material, 1,3,5-trithia-2,4,6-triazapentalenyl (TTTA), which is known for its photoinduced transition from the dimerized spin-singlet phase to the regular paramagnetic phase. We conclude that the lowest photoexcited state of TTTA is the interdimer CT exciton state and the second lowest state is the intradimer CT exciton state.

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arXiv2007

Charge ordering in θ-(BEDT-TTF)2RbZn(SCN)4: Cooperative effects of electron correlations and lattice distortions

Combined effects of electron correlations and lattice distortions are investigated on the charge ordering in θ-(BEDT-TTF)2RbZn(SCN)4 theoretically in a two-dimensional 3/4-filled extended Hubbard model with electron-lattice couplings. It is known that this material undergoes a phase transition from a high-symmetry metallic state to a low-symmetry insulating state with a horizontal-stripe charge order (CO) by lowering temperature. By means of the exact-diagonalization method, we show that electron-phonon interactions are crucial to stabilize the horizontal-stripe CO and to realize the low-symmetry crystal structure.

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arXiv2006

Dynamics of photoexcited states in one-dimensional dimerized Mott insulators

Dynamical properties of photoexcited states are theoretically studied in a one-dimensional Mott insulator dimerized by the spin-Peierls instability. Numerical calculations combined with a perturbative analysis have revealed that the lowest photoexcited state without nearest-neighbor interaction corresponds to an interdimer charge transfer excitation that belongs to dispersive excitations. This excited state destabilizes the dimerized phase, leading to a photoinduced inverse spin-Peierls transition. We discuss the purely electronic origin of midgap states that are observed in a latest photoexcitation experiment of an organic spin-Peierls compound, K-TCNQ (potassium-tetracyanoquinodimethane).

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arXiv2006

Possibility of field-induced incommensurate order in quasi-one-dimensional frustrated spin system

We study an incommensurate long-range order induced by an external magnetic field in a quasi-one-dimensional bond-alternating spin system, F5PNN, focusing on the role of the frustrating interaction which can be enhanced by a high-pressure effect. On the basis of the density matrix renormalization group analysis of a microscopic model for F5PNN, we present several H-T phase diagrams for typical parameters of the frustrating next-nearest-neighbour coupling and the interchain interaction, and then discuss how the field-induced incommensurate order develops by the frustration effect in such phase diagrams. A magnetization plateau at half the saturation moment is also mentioned.

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arXiv2006

Interchain coupling effects on photoinduced phase transitions between neutral and ionic phases in an extended Hubbard model with alternating potentials and an electron-lattice coupling

Dynamics of ionic-to-neutral and neutral-to-ionic phase transitions induced by intrachain charge-transfer photoexcitations are studied in a quasi-one-dimensional extended Hubbard model with alternating potentials and an electron-lattice coupling for mixed-stack charge-transfer complexes. For interchain couplings, we use electron-electron interactions previously estimated for TTF-CA (TTF=tetrathiafulvalene, CA=chloranil). Photoexcitation is introduced by a pulse of oscillating electric field. The time-dependent Hartree-Fock approximation is used for the electronic part, and the classical approximation for the lattice part. In the ionic-to-neutral transition, the transferred charge density is a strongly nonlinear function of the photoexcitation density, which is characterized by the presence of a threshold. With substantial interchain couplings comparable to those in TTF-CA, the interchain correlation is strong during the transition. Neutral domains in nearby chains simultaneously grow even if their nucleation is delayed by reducing the amplitude of the electric field. With weaker interchain couplings, the growing processes are in phase only when the amplitude of the electric field is large. Thus, the experimentally observed, coherent motion of a macroscopic neutral-ionic domain boundary is allowed to emerge by such substantial interchain couplings. In the neutral-to-ionic transition, by contrast, the transferred charge density is almost a linear function of the photoexcitation density. Interchain electron-electron interactions make the function slightly nonlinear, but the uncooperative situation is almost unchanged and consistent with the experimental findings.

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arXiv2005

Theory of Photoinduced Phase Transitions

Theories of photoinduced phase transitions have developed along with the progress in experimental studies, especially concerning their nonlinear characters and transition dynamics. At an early stage, paths from photoinduced local structural distortions to global ones are explained in classical statistical models. Their dynamics are governed by transition probabilities and inevitably stochastic, but they were sufficient to describe coarse-grained time evolutions. Recently, however, a variety of dynamics including ultrafast ones are observed in different electronic states. They are explained in relevant electronic models. In particular, a coherent lattice oscillation and coherent motion of a macroscopic domain boundary need appropriate interactions among electrons and lattice displacements. Furthermore, some transitions proceed almost in one direction, which can be explained by considering relevant electronic processes. We describe the history of theories of photoinduced phase transitions and discuss a future perspective.

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arXiv2005

Photoinduced metallic properties of one-dimensional strongly correlated electron systems

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.

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arXiv2005

Mechanism of Ambipolar Field-Effect Carrier Injections in One-Dimensional Mott Insulators

To clarify the mechanism of recently reported, ambipolar carrier injections into quasi-one-dimensional Mott insulators on which field-effect transistors are fabricated, we employ the one-dimensional Hubbard model attached to a tight-binding model for source and drain electrodes. To take account of the formation of Schottky barriers, we add scalar and vector potentials, which satisfy the Poisson equation with boundary values depending on the drain voltage, the gate bias, and the work-function difference. The current-voltage characteristics are obtained by solving the time-dependent Schrödinger equation in the unrestricted Hartree-Fock approximation. Its validity is discussed with the help of the Lanczos method applied to small systems. We find generally ambipolar carrier injections in Mott insulators even if the work function of the crystal is quite different from that of the electrodes. They result from balancing the correlation effect with the barrier effect. For the gate-bias polarity with higher Schottky barriers, the correlation effect is weakened accordingly, owing to collective transport in the one-dimensional correlated electron systems.

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arXiv2004

Phase Transition in a One-Dimensional Extended Peierls-Hubbard Model with a Pulse of Oscillating Electric Field: I. Threshold Behavior in Ionic-to-Neutral Transition

Photoinduced dynamics of charge density and lattice displacements is calculated by solving the time-dependent Schrödinger equation for a one-dimensional extended Peierls-Hubbard model with alternating potentials for the mixed-stack organic charge-transfer complex, TTF-CA. A pulse of oscillating electric field is incorporated into the Peierls phase of the transfer integral. The frequency, the amplitude, and the duration of the pulse are varied to study the nonlinear and cooperative character of the photoinduced transition. When the dimerized ionic phase is photoexcited, the threshold behavior is clearly observed by plotting the final ionicity as a function of the increment of the total energy. Above the threshold photoexcitation, the electronic state reaches the neutral one with equidistant molecules after the electric field is turned off. The transition is initiated by nucleation of a metastable neutral domain, for which an electric field with frequency below the linear absorption peak is more effective than that at the peak. When the pulse is strong and short, the charge transfer takes place on the same time scale with the disappearance of dimerization. As the pulse becomes weak and long, the dimerization-induced polarization is disordered to restore the inversion symmetry on average before the charge transfer takes place to bring the system neutral. Thus, a paraelectric ionic phase is transiently realized by a weak electric field. It is shown that infrared light also induces the ionic-to-neutral transition, which is characterized by the threshold behavior.

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arXiv2004

Phase Transition in a One-Dimensional Extended Peierls-Hubbard Model with a Pulse of Oscillating Electric Field: II. Linear Behavior in Neutral-to-Ionic Transition

Dynamics of charge density and lattice displacements after the neutral phase is photoexcited is studied by solving the time-dependent Schrödinger equation for a one-dimensional extended Peierls-Hubbard model with alternating potentials. In contrast to the ionic-to-neutral transition studied previously, the neutral-to-ionic transition proceeds in an uncooperative manner as far as the one-dimensional system is concerned. The final ionicity is a linear function of the increment of the total energy. After the electric field is turned off, the electronic state does not significantly change, roughly keeping the ionicity, even if the transition is not completed, because the ionic domains never proliferate. As a consequence, an electric field with frequency just at the linear absorption peak causes the neutral-to-ionic transition the most efficiently. These findings are consistent with the recent experiments on the mixed-stack organic charge-transfer complex, TTF-CA. We artificially modify or remove the electron-lattice coupling to discuss the origin of such differences between the two transitions.

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arXiv2004

Phase Transition in a One-Dimensional Extended Peierls-Hubbard Model with a Pulse of Oscillating Electric Field: III. Interference Caused by a Double Pulse

In order to study consequences of the differences between the ionic-to-neutral and neutral-to-ionic transitions in the one-dimensional extended Peierls-Hubbard model with alternating potentials for the TTF-CA complex, we introduce a double pulse of oscillating electric field in the time-dependent Schrödinger equation and vary the interval between the two pulses as well as their strengths. When the dimerized ionic phase is photoexcited, the interference effect is clearly observed owing to the coherence of charge density and lattice displacements. Namely, the two pulses constructively interfere with each other if the interval is a multiple of the period of the optical lattice vibration, while they destructively interfere if the interval is a half-odd integer times the period, in the processes toward the neutral phase. The interference is strong especially when the pulse is strong and short because the coherence is also strong. Meanwhile, when the neutral phase is photoexcited, the interference effect is almost invisible or weakly observed when the pulse is weak. The photoinduced lattice oscillations are incoherent due to random phases. The strength of the interference caused by a double pulse is a key quantity to distinguish the two transitions and to evaluate the coherence of charge density and lattice displacements.

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