arXiv subjects

Eva Pavarini

Publications and source records attributed to Eva Pavarini.

15 recordsLinked to original sources

arXiv2024

Origin of the transitions inversion in rare-earth vanadates

The surprising inversion of the orbital- and magnetic-order transition temperatures in the RVO3 series with increasing the rare-earth radius makes the series unique among orbitally-ordered materials. Here, augmenting dynamical mean-field theory with a decomposition of the order parameter into irreducible tensors, we show that this anomalous behavior emerges from an unusual hierarchy of interactions. First, increasing the rare-earth radius, orbital physics comes to be controlled by xz-xz quadrupolar super-exchange rather than by lattice distortion. Next, for antiferromagnetic spin order, orbital super-exchange terms with different spin rank compete, so that the dipolar spin-spin interaction dominates. Eventually, G-type magnetic order (anti-ferro in all directions) can appear already above the orbital ordering transition, and C-type order (anti-ferro in the ab plane) right around it. The strict constraints we found explain why the inversion is rare, giving at the same time criteria to look for similar behavior in other materials.

cond-mat.str-el↗

arXiv2022

LaVO$_3$: a true Kugel-Khomskii system

We show that the $t_{2g}^2$ perovskite LaVO$_3$, in its orthorhombic phase, is a rare case of a system hosting an orbital-ordering Kugel-Khomskii phase transition, rather than being controlled by the Coulomb-enhanced crystal-field splitting. We find that, as a consequence of this, the magnetic transition is close to (and even above) the super-exchange driven orbital-ordering transition, whereas typically magnetism arises at much lower temperatures than orbital ordering. Our results support the experimental scenario of orbital-ordering and G-type spin correlations just above the monoclinic-to-orthorhombic structural change. To explore the effects of crystal-field splitting and filling, we compare to YVO$_3$ and $t_{2g}^1$ titanates. In all these materials the crystal-field is sufficiently large to suppress the Kugel-Khomskii phase transition.

cond-mat.str-el↗

arXiv2022

Constraints on the two-dimensional pseudo-spin 1/2 Mott insulator description of Sr$_2$IrO$_4$

Sr$_{2}$IrO$_{4}$ has often been described via a simple, one-band pseudo-spin 1/2 model, subject to electron-electron interactions, on a square lattice, fostering analogies with cuprate superconductors, believed to be well described by a similar model. In this work we argue - based on a detailed study of the low-energy electronic structure by circularly polarized spin and angle-resolved photoemission spectroscopy combined with dynamical mean-field theory calculations - that a pseudo-spin 1/2 model fails to capture the full complexity of the system. We show instead that a realistic multi-band Hubbard Hamiltonian, accounting for the full correlated $t_{2g}$ manifold, provides a detailed description of the interplay between spin-orbital entanglement and electron-electron interactions, and yields quantitative agreement with experiments. Our analysis establishes that the $j_{3/2}$ states make up a substantial percentage of the low energy spectral weight, i.e. approximately 74% as determined from the integration of the $j$-resolved spectral function in the $0$ to $-1.64$ eV energy range. The results in our work are not only of relevance to iridium based materials, but more generally to the study of multi-orbital materials with closely spaced energy scales.

cond-mat.str-el↗

arXiv2019

First-principles many-body models for electron transport through molecular nanomagnets

Impressive advances in the field of molecular spintronics allow one to study electron transport through individual magnetic molecules embedded between metallic leads in the purely quantum regime of single electron tunneling. Besides fundamental interest, this experimental setup, in which a single molecule is manipulated by electronic means, provides the elementary units of possible forthcoming technological applications, ranging from spin valves to transistors and qubits for quantum information processing. Theoretically, while for weakly correlated molecular junctions established first-principles techniques do enable the system-specific description of transport phenomena, methods of similar power and flexibility are still lacking for junctions involving strongly correlated molecular nanomagnets. Here we propose an efficient scheme based on the ab initio construction of material-specific Hubbard models and on the master-equation formalism. We apply this approach to a representative case, the Ni$_2$ molecular spin dimer, in the regime of weak molecule-electrode coupling, the one relevant for quantum-information applications. Our approach allows us to study in a realistic setting many-body effects such as current suppression and negative differential conductance. We think that this method has the potential for becoming a very useful tool for describing transport phenomena in strongly correlated molecules.

cond-mat.str-el↗

arXiv2016

The Fermi surface of Sr2RuO4: spin-orbit and anisotropic Coulomb interaction effects

The topology of the Fermi surface of Sr2RuO4 is well described by local-density approximation calculations with spin-orbit interaction, but the relative size of its different sheets is not. By accounting for many-body effects via dynamical mean-field theory, we show that the standard isotropic Coulomb interaction alone worsens or does not correct this discrepancy. In order to reproduce experiments, it is essential to account for the Coulomb anisotropy. The latter is small but has strong effects; it competes with the Coulomb-enhanced spin-orbit coupling and the isotropic Coulomb term in determining the Fermi surface shape. Its effects are likely sizable in other correlated multi-orbital systems. In addition, we find that the low-energy self-energy matrix -- responsible for the reshaping of the Fermi surface -- sizably differ from the static Hartree-Fock limit. Finally, we find a strong spin-orbital {entanglement}; this supports the view that the conventional description of Cooper pairs via factorized spin and orbital part might not apply to Sr2RuO4.

cond-mat.str-el↗

arXiv2016

Thermally assisted ordering in Mott insulators

Ginzburg-Landau theory describes phase transitions as the competition between energy and entropy: The ordered phase has lower energy, while the disordered phase has larger entropy. When heating the system, ordering is reduced entropically until it vanishes at the critical temperature. This established picture implicitly assumes that the energy difference between ordered and disordered phase does not change with temperature. We show that for the Mott insulator KCuF3 this assumption is strongly violated: thermal expansion energetically stabilizes the orbitally-ordered phase to such and extent that no phase transition is observed. This new mechanism explains not only the absence of a phase transition in KCuF3 but even suggests the possibility of an inverted transition in closed-shell systems, where the ordered phase emerges only at high temperatures.

cond-mat.str-el↗

arXiv2014

Electronic Structure Calculations with LDA+DMFT

The LDA+DMFT method is a very powerful tool for gaining insight into the physics of strongly correlated materials. It combines traditional ab-initio density-functional techniques with the dynamical mean-field theory. The core aspects of the method are (i) building material-specific Hubbard-like many-body models and (ii) solving them in the dynamical mean-field approximation. Step (i) requires the construction of a localized one-electron basis, typically a set of Wannier functions. It also involves a number of approximations, such as the choice of the degrees of freedom for which many-body effects are explicitly taken into account, the scheme to account for screening effects, or the form of the double-counting correction. Step (ii) requires the dynamical mean-field solution of multi-orbital generalized Hubbard models. Here central is the quantum-impurity solver, which is also the computationally most demanding part of the full LDA+DMFT approach. In this chapter I will introduce the core aspects of the LDA+DMFT method and present a prototypical application.

cond-mat.str-el↗

arXiv2013

Mechanism of structural phase transitions in KCrF3

We study the origin of the cubic to tetragonal and tetragonal to monoclinic structural transitions in KCrF3, and the associated change in orbital order, paying particular attention to the relevance of super-exchange in both phases. We show that super-exchange is not the main mechanism driving these transitions. Specifically, it is not strong enough to be responsible for the high-temperature cubic to tetragonal transition and does not yield the type of orbital order observed in the monoclinic phase. The energy difference between the tetragonal and the monoclinic structure is tiny, and most likely results from the interplay between volume, covalency, and localization effects. The transition is rather driven by Slater exchange than super-exchange. Nevertheless, once the monoclinic distortions are present, super-exchange helps in stabilizing the low symmetry structure. The orbital order we obtain for this monoclinic phase is consistent with the magnetic transition at 80 K.

cond-mat.str-el↗

arXiv2013

Multiplet effects in orbital and spin ordering phenomena: A hybridization-expansion quantum impurity solver study

Orbital and spin ordering phenomena in strongly correlated systems are commonly studied using the local-density approximation + dynamical mean-field theory approach. Typically, however, such simulations are restricted to simplified models (density-density Coulomb interactions, high symmetry couplings and few-band models). In this work we implement an efficient general hybridization-expansion continuous-time quantum Monte Carlo impurity solver (Krylov approach) which allows us to investigate orbital and spin ordering in a more realistic setting, including interactions that are often neglected (e.g., spin-flip and pair-hopping terms), enlarged basis sets (full d versus eg), low-symmetry distortions, and reaching the very low-temperature (experimental) regime. We use this solver to study ordering phenomena in a selection of exemplary low-symmetry transition-metal oxides: LaMnO3 and rare-earth manganites as well as the perovskites CaVO3 and YTiO3. We show that spin-flip and pair hopping terms do not affect the Kugel-Khomskii orbital-order melting transition in rare-earth manganites, or the suppression of orbital fluctuations driven by crystal field and Coulomb repulsion. For the Mott insulator YTiO3 we find a ferromagnetic transition temperature 50 K, in remarkably good agreement with experiments. For LaMnO3 we show that the classical t2g-spin approximation, commonly adopted for studying manganites, yields indeed an occupied eg orbital in very good agreement with that obtained for the full d 5-orbital Hubbard model, while the spin-spin e_g-t_{2g} correlation function calculated from the full d model is 0.74, very close to the value expected for aligned eg and t2g spins; the eg spectral function matrix is also well reproduced. Finally, we show that the t2g screening reduces the eg-eg Coulomb repulsion by about 10%

cond-mat.str-el↗

arXiv2012

Importance of exchange-anisotropy and superexchange for the spin-state transitions in LnCoO3 (Ln=La,Y,RE) cobaltates

Spin-state transitions are the hallmark of rare-earth cobaltates. In order to understand them, it is essential to identify all relevant parameters which shift the energy balance between spin states, and determine their trends. We find that Δ, the eg-t2g crystal-field splitting, increases by ~250 meV when increasing pressure to 8 GPa and by about 150 meV when cooling from 1000K to 5K. It changes, however, by less than 100 meV when La is substituted with another rare earth. Also the Hund's rule coupling J_avg is about the same in systems with very different spin-state transition temperature, like LaCoO3 and EuCoO3. Consequently, in addition to Δand J_avg, the Coulomb-exchange anisotropy ΔJ_ avg and the super-exchange energy-gain ΔE_SE play a crucial role, and are comparable with spin-state dependent relaxation effects due to covalency. We show that in the LnCoO3 series, with Ln=Y or a rare earth (RE), super-exchange progressively stabilizes a low-spin ground state as the Ln^{3+} ionic radius decreases. We give a simple model to describe spin-state transitions and show that, at low temperature, the formation of isolated high-spin/low-spin pairs is favored, while in the high-temperature phase, the most likely homogeneous state is high-spin, rather than intermediate spin. An orbital-selective Mott state could be a fingerprint of such a state.

cond-mat.str-el↗

arXiv2011

Orbital-order melting in rare-earth manganites: the role of super-exchange

We study the mechanism of orbital-order melting observed at temperature T_OO in the series of rare-earth manganites. We find that many-body super-exchange yields a transition-temperature T_KK that decreases with decreasing rare-earth radius, and increases with pressure, opposite to the experimental T_OO. We show that the tetragonal crystal-field splitting reduces T_KK further increasing the discrepancies with experiments. This proves that super-exchange effects, although very efficient, in the light of the experimentally observed trends, play a minor role for the melting of orbital ordering in rare-earth manganites.

cond-mat.str-el↗

arXiv2010

Origin of Jahn-Teller distortion and orbital-order in LaMnO3

The origin of the cooperative Jahn-Teller distortion and orbital-order in LaMnO3 is central to the physics of the manganites. The question is complicated by the simultaneous presence of tetragonal and GdFeO3-type distortions and the strong Hund's rule coupling between e_g and t_2g electrons. To clarify the situation we calculate the transition temperature for the Kugel-Khomskii superexchange mechanism by using the local density approximation+dynamical mean-field method, and disentangle the effects of super-exchange from those of lattice distortions. We find that super-exchange alone would yield T_KK=650 K. The tetragonal and GdFeO3-type distortions, however, reduce T_KK to 550 K. Thus electron-phonon coupling is essential to explain the persistence of local Jahn-Teller distortions to at least 1150 K and to reproduce the occupied orbital deduced from neutron scattering.

cond-mat.str-el↗

arXiv2001

NMR relaxation rates and Knight shifts in MgB2

We calculate ab initio the NMR relaxation rates and the Knight shifts in MgB_2. We show that the dominant relaxation mechanism at the B nucleus is the interaction with the electronic orbital moment, and we give a simple explanation of that using a simple $sp$ tight binding model. When Stoner enhancement (also calculated ab-initio) is accounted for, we obtain good agreement with reported experimental values. For the 25Mg nucleus, we predict that the dominant relaxation mechanism is the Fermi-contact interaction, which also dominates the Mg Knight shift.

cond-mat.supr-con↗

arXiv2001

Electronic structure and string tension of stripes in high-Tc superconductors

We present a simple, material-specific model Hamiltonian for stripes and use it to explain the observed differences between the angle-resolved photoemission spectra of La(2-x)Sr(x)CuO4 and Bi(2)Sr(2)CaCu(2)O(8+x), e.g, along the nodal line and around (3pi/4,0). Next we compute the string tension for stripes and find it to be smallest in the materials with the highest observed Tc,max.

cond-mat↗

arXiv2000

Ab initio calculation of resonant X-ray scattering in Manganites

We study the origin of the resonant x-ray signal in manganites and generalize the resonant cross-section to the band structure framework. With {\it ab initio} LSDA and LSDA+U calculations we determine the resonant x-ray spectrum of LaMnO$_3$. The calculated spectrum and azimuthal angle dependence at the Mn $K$-edge reproduce the measured data without adjustable parameters. The intensity of this signal is directly related to the orthorhombicity of the lattice. We also predict a resonant x-ray signal at the La $L$-edge, caused by the tilting of the MnO$_6$ octahedra. This shows that the resonant x-ray signal in the hard x-ray regime can be understood in terms of the band structure of a material and is sensitive to the fine details of crystal structure.

cond-mat.str-el↗