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M. Eckstein

Publications and source records attributed to M. Eckstein.

11 recordsLinked to original sources

Sub-cycle multidimensional spectroscopy of strongly correlated materials

Strongly correlated solids are extremely complex and fascinating quantum systems, where new states continue to emerge, especially when interaction with light triggers interplay between them. In this interplay, sub-laser-cycle electron response is particularly attractive as a tool for ultrafast manipulation of matter at PHz scale. Here we introduce a new type of non-linear multidimensional spectroscopy, which allows us to unravel the sub-cycle dynamics of strongly correlated systems interacting with few-cycle infrared pulses and the complex interplay between different correlated states evolving on the sub-femtosecond time-scale. We demonstrate that single particle sub-cycle electronic response is extremely sensitive to correlated many-body dynamics and provides direct access to many body response functions. For the two-dimensional Hubbard model under the influence of ultra-short, intense electric field transients, we demonstrate that our approach can resolve pathways of charge and energy flow between localized and delocalized many-body states on the sub-cycle time scale and follow the creation of a highly correlated state surviving after the end of the laser pulse. Our findings open a way towards a regime of imaging and manipulating strongly correlated materials at optical rates, beyond the multi-cycle approach employed in Floquet engineering, with the sub-cycle response being a key tool for accessing many body phenomena.

cond-mat.str-el

Dynamically induced doublon repulsion in the Fermi-Hubbard model probed by a single-particle density of states

We investigate the possibility to control dynamically the interactions between repulsively bound pairs of fermions (doublons) in correlated systems with off-resonant ac fields. We introduce an effective Hamiltonian that describes the physics of doublons up to the second-order in the high-frequency limit. It unveils that the doublon interaction, which is attractive in equilibrium, can be completely suppressed and then switched to repulsive by varying the power of the ac field. We show that the signature of the dynamical repulsion between doublons can be found in the single-fermion density of states averaged in time. Our results are further supported by nonequilibrium dynamical mean-field theory simulations for the half-filled Fermi-Hubbard model.

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Optical control of competing exchange interactions and coherent spin-charge coupling in two-orbital Mott insulators

In order to have a better understanding of ultrafast electrical control of exchange interactions in multi-orbital systems, we study a two-orbital Hubbard model at half filling under the action of a time-periodic electric field. Using suitable projection operators and a generalized time-dependent canonical transformation, we derive an effective Hamiltonian which describes two different regimes. First, for a wide range of non-resonant frequencies, we find a change of the bilinear Heisenberg exchange $J_{\textrm{ex}}$ that is analogous to the single-orbital case. Moreover we demonstrate that also the additional biquadratic exchange interaction $B_{\textrm{ex}}$ can be enhanced, reduced and even change sign depending on the electric field. Second, for special driving frequencies, we demonstrate a novel spin-charge coupling phenomenon enabling coherent transfer between spin and charge degrees of freedom of doubly ionized states. These results are confirmed by an exact time-evolution of the full two-orbital Mott-Hubbard Hamiltonian.

cond-mat.str-el

Ultrafast and reversible control of the exchange interaction in Mott insulators

The strongest interaction between microscopic spins in magnetic materials is the exchange interaction $J_\text{ex}$. Therefore, ultrafast control of $J_\text{ex}$ holds the promise to control spins on ultimately fast timescales. We demonstrate that time-periodic modulation of the electronic structure by electric fields can be used to reversibly control $J_\text{ex}$ on ultrafast timescales in extended antiferromagnetic Mott insulators. In the regime of weak driving strength, we find that $J_\text{ex}$ can be enhanced and reduced for frequencies below and above the Mott gap, respectively. Moreover, for strong driving strength, even the sign of $J_\text{ex}$ can be reversed and we show that this causes time reversal of the associated quantum spin dynamics. These results suggest wide applications, not only to control magnetism in condensed matter systems, for example, via the excitation of spin resonances, but also to assess fundamental questions concerning the reversibility of the quantum many-body dynamics in cold atom systems.

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Inverse magneto-refraction as a mechanism for laser modification of spin-spin exchange parameters and subsequent terahertz emission from iron oxides

Ultrafast non-thermal manipulation of magnetization by light relies on either indirect coupling of the electric field component of the light with spins via spin-orbit interaction or direct coupling between the magnetic field component and spins. Here we propose a novel scenario for coupling between the electric field of light and spins via optical modification of the exchange interaction, one of the strongest quantum effects, the strength of which can reach 1000 Tesla. We demonstrate that this isotropic opto-magnetic effect, which can be called the inverse magneto-refraction, is allowed in a material of any symmetry. Its existence is corroborated by the experimental observation of THz emission by magnetic-dipole active spin resonances optically excited in a broad class of iron oxides with a canted spin configuration. From its strength we estimate that a sub-picosecond laser pulse with a moderate fluence of ~ 1 mJ/cm^2 acts as a pulsed effective magnetic field of 0.01 Tesla, arising from the optically perturbed balance between the exchange parameters. Our findings are supported by a low-energy theory for the microscopic magnetic interactions between non-equilibrium electrons subjected to an optical field which suggests a possibility to modify the exchange interactions by light over 1 %.

cond-mat.str-el

Ultrafast Quenching of the Exchange Interaction in a Mott Insulator

We investigate how fast and how effective photocarrier excitation can modify the exchange interaction $J_\mathrm{ex}$ in the prototype Mott-Hubbard insulator. We demonstrate an ultrafast quenching of $J_\mathrm{ex}$ both by evaluating exchange integrals from a time-dependent response formalism and by explicitly simulating laser-induced spin precession in an antiferromagnet that is canted by an external magnetic field. In both cases, the electron dynamics is obtained from nonequilibrium dynamical mean-field theory. We find that the modified $J_\mathrm{ex}$ emerges already within a few electron hopping times after the pulse, with a reduction that is comparable to the effect of chemical doping.

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Field-assisted doublon manipulation in the Hubbard model. A quantum doublon ratchet

For the fermionic Hubbard model at strong coupling, we demonstrate that directional transport of localized doublons (repulsively bound pairs of two particles occupying the same site of the crystal lattice) can be achieved by applying an unbiased ac field of time-asymmetric (sawtooth-like) shape. The mechanism involves a transition to intermediate states of virtually zero double occupation which are reached by splitting the doublon by fields of the order of the Hubbard interaction. The process is discussed on the basis of numerically exact calculations for small clusters, and we apply it to more complex states to manipulate the charge order pattern of one-dimensional systems.

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New theoretical approaches for correlated systems in nonequilibrium

We review recent developments in the theory of interacting quantum many-particle systems that are not in equilibrium. We focus mainly on the nonequilibrium generalizations of the flow equation approach and of dynamical mean-field theory (DMFT). In the nonequilibrium flow equation approach one first diagonalizes the Hamiltonian iteratively, performs the time evolution in this diagonal basis, and then transforms back to the original basis, thereby avoiding a direct perturbation expansion with errors that grow linearly in time. In nonequilibrium DMFT, on the other hand, the Hubbard model can be mapped onto a time-dependent self-consistent single-site problem. We discuss results from the flow equation approach for nonlinear transport in the Kondo model, and further applications of this method to the relaxation behavior in the ferromagnetic Kondo model and the Hubbard model after an interaction quench. For the interaction quench in the Hubbard model, we have also obtained numerical DMFT results using quantum Monte Carlo simulations. In agreement with the flow equation approach they show that for weak coupling the system relaxes to a "prethermalized" intermediate state instead of rapid thermalization. We discuss the description of nonthermal steady states with generalized Gibbs ensembles.

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Phase separation in the particle-hole asymmetric Hubbard model

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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Isosbestic points in the spectral function of correlated electrons

We investigate the properties of the spectral function A(omega,U) of correlated electrons within the Hubbard model and dynamical mean-field theory. Curves of A(omega,U) vs. omega for different values of the interaction U are found to intersect near the band-edges of the non-interacting system. For a wide range of U the crossing points are located within a sharply confined region. The precise location of these 'isosbestic points' depends on details of the non-interacting band structure. Isosbestic points of dynamic quantities therefore provide valuable insights into microscopic energy scales of correlated systems.

cond-mat.str-el

Green functions for nearest- and next-nearest-neighbor hopping on the Bethe lattice

We calculate the local Green function for a quantum-mechanical particle with hopping between nearest and next-nearest neighbors on the Bethe lattice, where the on-site energies may alternate on sublattices. For infinite connectivity the renormalized perturbation expansion is carried out by counting all non-self-intersecting paths, leading to an implicit equation for the local Green function. By integrating out branches of the Bethe lattice the same equation is obtained from a path integral approach for the partition function. This also provides the local Green function for finite connectivity. Finally, a recently developed topological approach is extended to derive an operator identity which maps the problem onto the case of only nearest-neighbor hopping. We find in particular that hopping between next-nearest neighbors leads to an asymmetric spectrum with additional van-Hove singularities.

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