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Register a new userPhotoinduced enhancement of bond-order in the one-dimensional extended Hubbard model
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We investigate the real-time dynamics of the half-filled one-dimensional extended Hubbard model in the strong-coupling regime, when driven by a transient laser pulse. Starting from a wide regime displaying a charge-density wave in equilibrium, a robust photoinduced in-gap state appears in the optical conductivity, depending on the parameters of the pulse. Here, by tuning its conditions, we maximize the overlap of the time-evolving wavefunction with excited states displaying the elusive bond-ordered wave of this model. Finally, we make a clear connection between the emergence of this order and the formation of the aforementioned in-gap state, suggesting the potential observation of purely electronic (i.e., not associated with a Peierls instability) bond-ordered waves in experiments involving molecular crystals.
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Photoinduced dynamics in an excitonic insulator is studied theoretically by using a two-orbital Hubbard model on the square lattice where the excitonic phase in the ground state is characterized by the BCS-BEC crossover as a function of the interorbital Coulomb interaction. We consider the case where the order has a wave vector $Q=(0,0)$ and photoexcitation is introduced by a dipole transition. Within the mean-field approximation, we show that the excitonic order can be enhanced by the photoexcitation when the system is initially in the BEC regime of the excitonic phase, whereas it is reduced if the system is initially in the BCS regime. The origin of this difference is discussed from behaviors of momentum distribution functions and momentum-dependent excitonic pair condensation. In particular, we show that the phases of the excitonic pair condensation have an important role in determining whether the excitonic order is enhanced or not.
We study photoinduced ultrafast coherent oscillations originating from orbital degrees of freedom in the one-dimensional two-orbital Hubbard model. By solving the time-dependent Schrodinger equation for the numerically exact many-electron wave function, we obtain time-dependent optical response functions. The calculated spectra show characteristic coherent oscillations that vary with the frequency of probe light. A simple analysis for the dominant oscillating components clarifies that these photoinduced oscillations are caused by the quantum interference between photogenerated states. The oscillation attributed to the Raman-active orbital excitations (orbitons) clearly appears around the charge-transfer peak.
Using time-dependent density-matrix renormalization group, we study the time evolution of electronic wave packets in the one-dimensional extended Hubbard model with on-site and nearest neighbor repulsion, U and V, respectively. As expected, the wave packets separate into spin-only and charge-only excitations (spin-charge separation). Charge and spin velocities exhibit non-monotonic dependence on V. For small and intermediate values of V, both velocities increase with V. However, the charge velocity exhibits a stronger dependence than that of the spin, leading to a more pronounced spin-charge separation. Charge fractionalization, on the other hand, is weakly affected by V. The results are explained in terms of Luttinger liquid theory in the weak-coupling limit, and an effective model in the strong-coupling regime.
We consider the one-dimensional extended Hubbard model in the presence of an explicit dimerization $delta$. For a sufficiently strong nearest neighbour repulsion we establish the existence of a quantum phase transition between a mixed bond-order wave and charge-density wave phase from a pure bond-order wave phase. This phase transition is in the universality class of the two-dimensional Ising model.
We investigate the $T=0$ phase diagram of a variant of the one-dimensional extended Hubbard model where particles interact via a finite-range soft-shoulder potential. Using Density Matrix Renormalization Group (DMRG) simulations, we evidence the appearance of Cluster Luttinger Liquid (CLL) phases, similarly to what first predicted in a hard-core bosonic chain [M. Mattioli, M. Dalmonte, W. Lechner, and G. Pupillo, Phys. Rev. Lett. 111, 165302]. As the interaction strength parameters change, we find different types of clusters, that encode the order of the ground state in a semi-classical approximation and give rise to different types of CLLs. Interestingly, we find that the conventional Tomonaga Luttinger Liquid (TLL) is separated by a critical line with a central charge $c=5/2$, along which the two (spin and charge) bosonic degrees of freedom (corresponding to $c=1$ each) combine in a supersymmetric way with an emergent fermionic excitation ($c=1/2$). We also demonstrate that there are no significant spin correlations.
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