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Register a new userPhase Separation Induced by Symmetric Monocycle Optical Pulse in Extended Hubbard Models
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Many-electron dynamics induced by a symmetric monocycle electric-field pulse of large amplitude is theoretically investigated in one- and two-dimensional half-filled extended Hubbard models on regular lattices (i.e., without dimerization) using the exact diagonalization method for small systems and the Hartree-Fock approximation for large systems. The formation of a negative-temperature state and the change from repulsive interactions to effective attractive interactions are shown to be realized for a wide region of the field amplitude and the excitation energy. For a nonnegligible intersite repulsive interaction, the numerical results are consistent with the fact that the phase separation between charge-rich and charge-poor regions is caused by the corresponding effective attraction.
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The excited state dynamics of correlated electron and electron-phonon systems triggered by an oscillating electric-field pulse of large amplitude are theoretically investigated. A negative-temperature state and inversion of electron-electron and electron-phonon interactions are induced even by a symmetric monocycle pulse. This fact is numerically demonstrated, using the exact diagonalization method, in a band-insulator phase of one-dimensional three-quarter-filled strongly dimerized extended Peierls-Hubbard and Holstein models. When the total-energy increment is maximized as a function of the electric field amplitude, the occupancy of the bonding and antibonding orbitals is inverted to produce a negative-temperature state. Around this state, the dependences of time-averaged electron-electron and electron-phonon correlation functions on interaction parameters are opposite to those in the ground state.
Using a high-frequency expansion in periodically driven extended Hubbard models, where the strengths and ranges of density-density interactions are arbitrary, we obtain the effective interactions and bandwidth, which depend sensitively on the polarization of the driving field. Then, we numerically calculate modulations of correlation functions in a quarter-filled extended Hubbard model with nearest-neighbor interactions on a triangular lattice with trimers after monocycle pulse excitation. We discuss how the resultant modulations are compatible with the effective interactions and bandwidth derived above on the basis of their dependence on the polarization of photoexcitation, which is easily accessible by experiments. Some correlation functions after monocycle pulse excitation are consistent with the effective interactions, which are weaker or stronger than the original ones. However, the photoinduced enhancement of anisotropic charge correlations previously discussed for the three-quarter-filled organic conductor $alpha$-(bis[ethylenedithio]-tetrathiafulvalene)$_2$I$_3$ [$alpha$-(BEDT-TTF)$_2$I$_3$] in the metallic phase is not fully explained by the effective interactions or bandwidth, which are derived independently of the filling.
We consider a dynamical phase transition induced by a short optical pulse in a system prone to thermodynamical instability. We address the case of pumping to excitons whose density contributes directly to the order parameter. To describe both thermodynamic and dynamic effects on equal footing, we adopt a view of the excitonic insulator for the phase transition and suggest a formation of the Bose condensate for the pumped excitons. The work is motivated by experiments in donor-acceptor organic compounds with a neutral-ionic phase transition coupled to the spontaneous lattice dimerization and to charge transfer excitons. The double nature of the ensemble of excitons leads to an intricate time evolution, in particular to macroscopic quantum oscillations from the interference between the Bose condensate of excitons and the ground state of the excitonic insulator. The coupling of excitons and the order parameter also leads to self-trapping of their wave function, akin to self-focusing in optics. The locally enhanced density of excitons can surpass a critical value to trigger the phase transformation, even if the mean density is below the required threshold. The system is stratified in domains that evolve through dynamical phase transitions and sequences of merging.
Metal-insulator transitions (MIT) belong to a class of fascinating physical phenomena, which includes superconductivity, and colossal magnetoresistance (CMR), that are associated with drastic modifications of electrical resistance. In transition metal compounds, MIT are often related to the presence of strong electronic correlations that drive the system into a Mott insulator state. In these systems the MIT is usually tuned by electron doping or by applying an external pressure. However, it was noted recently that a Mott insulator should also be sensitive to other external perturbations such as an electric field. We report here the first experimental evidence of a non-volatile electric-pulse-induced insulator-to-metal transition and possible superconductivity in the Mott insulator GaTa4Se8. Our Scanning Tunneling Microscopy experiments show that this unconventional response of the system to short electric pulses arises from a nanometer scale Electronic Phase Separation (EPS) generated in the bulk material.
The paramagnetic phase diagram of the Hubbard model with nearest-neighbor (NN) and next-nearest-neighbor (NNN) hopping on the Bethe lattice is computed at half-filling and in the weakly doped regime using the self-energy functional approach for dynamical mean-field theory. NNN hopping breaks the particle-hole symmetry and leads to a strong asymmetry of the electron-doped and hole-doped regimes. Phase separation occurs at and near half-filling, and the critical temperature of the Mott transition is strongly suppressed.
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