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C. Franchini

Publications and source records attributed to C. Franchini.

At least 19 recordsLinked to original sources

Extending the Feynman variational principle and analytical methods to lattice polarons

We develop and compare several analytical approximations for the ground state and zero-temperature polaron dispersion in finite-width, nonparabolic conduction bands. The main focus of the work is an extension of the Feynman variational method to a tight-binding lattice, where the effective-mass approximation is no longer applicable. The resulting variational formulation is not restricted to a specific phonon dispersion or electron-phonon interaction and provides a uniform description across weak-, intermediate-, and strong-coupling regimes. In addition, we revisit and generalize other analytical approaches traditionally formulated for continuum polarons, including canonical transformations and self-consistent Wigner-Brillouin-type approximations. For lattice polarons, these methods exhibit qualitative features absent in the continuum case, such as a nontrivial connection between weak- and strong-coupling limits. We show that an improved Wigner-Brillouin scheme yields a momentum-dependent polaron self-energy free of resonances and in good agreement with numerically exact results. All methods are applied to the Holstein model on a tight-binding lattice and are benchmarked against numerically exact calculations, including diagrammatic Monte Carlo (both our calculations and preceding works) and exact diagonalization results. Furthermore, the analytical approaches are extended to polarons with Rashba-type spin-orbit coupling, providing a stringent test of their applicability in systems with nontrivial band structure. Our results demonstrate that the modified Feynman variational method yields ground-state energies and dispersions with accuracy comparable to, and in many cases exceeding, that of other established analytical approaches. The developed framework offers a versatile and reliable analytical description of lattice polarons beyond the continuum approximation.

cond-mat.str-el

The origin of magnetism in a supposedly nonmagnetic osmium oxide

A supposedly nonmagnetic 5d$^1$ double perosvkite oxide is investigated by a combination of spectroscopic and theoretical methods, namely resonant inelastic X-ray scattering, X-ray absorption spectroscopy, magnetic circular dichroism, and multiplet ligand field calculations. We found that the large spin-orbit coupling admixes the 5d $t_{2g}$ and $e_g$ orbitals, covalency raises the 5d population well above the nominal value, and the local symmetry is lower than $O_h$. The obtained electronic interactions account for the finite magnetic moment of Os in this compound and, in general, of 5d$^1$ ions. Our results provide direct evidence of elusive Jahn-Teller distortions, hinting at a strong electron-lattice coupling.

cond-mat.str-el

Effects of charge doping on Mott insulator with strong spin-orbit coupling, Ba$_2$NaOsO$_6$

The effects of doping on the electronic evolution of the Mott insulating state have been extensively studied in efforts to understand mechanisms of emergent quantum phases of materials. The study of these effects becomes ever more intriguing in the presence of entanglement between spin and orbital degrees of freedom. Here, we present a comprehensive investigation of charge doping in the double perovskite Ba$_2$NaOsO$_6$, a a complex Mott insulator where such entanglement plays an important role. We establish that the insulating magnetic ground state evolves from canted antiferromagnet (cAF)to N\'eel order for dopant levels exceeding ~ 10 %. Furthermore, we determine that a broken local point symmetry (BLPS) phase, precursor to the magnetically ordered state, occupies an extended portion of the (H-T) phase diagram with increased doping. This finding reveals that the breaking of the local cubic symmetry is driven by a multipolar order, most-likely of the antiferro-quadrupolar type.

cond-mat.str-el

Pressure-induced excitations in the out-of-plane optical response of the nodal-line semimetal ZrSiS

The anisotropic optical response of the layered, nodal-line semimetal ZrSiS at ambient and high pressure is investigated by frequency-dependent reflectivity measurements for the polarization along and perpendicular to the layers. The highly anisotropic optical conductivity is in very good agreement with results from density functional theory calculations and confirms the anisotropic character of ZrSiS. Whereas the in-plane optical conductivity shows only modest pressure-induced changes, we found strong effects on the out-of-plane optical conductivity spectrum of ZrSiS, with the appearance of two prominent excitations. These pronounced pressure-induced effects can neither be attributed to a structural phase transition according to our single-crystal x-ray diffraction measurements, nor can they be explained by electronic correlation and electron-hole pairing effects, as revealed by theoretical calculations. Our findings are discussed in the context of the recently proposed excitonic insulator phase in ZrSiS.

cond-mat.mtrl-sci

Optical response of an interacting polaron gas in strongly polar crystals

Optical conductivity of an interacting polaron gas is calculated within an extended random phase approximation which takes into account mixing of collective excitations of the electron gas with LO phonons. This mixing is important for the optical response of strongly polar crystals where the static dielectric constant is rather high: strontium titanate is the case. The present calculation sheds light on unexplained features of experimentally observed optical conductivity spectra in $n$-doped SrTiO$_{3}$. These features appear to be due to dynamic screening of the electron-electron interaction by polar optical phonons and hence do not require additional mechanisms for the explanation.

cond-mat.str-el

Spin fluctuation induced Weyl semimetal state in the paramagnetic phase of EuCd$_2$As$_2$

Weyl fermions as emergent quasiparticles can arise in Weyl semimetals (WSMs) in which the energy bands are nondegenerate, resulting from inversion or time-reversal symmetry breaking. Nevertheless, experimental evidence for magnetically induced WSMs is scarce. Here, using photoemission spectroscopy, we observe that the degeneracy of Bloch bands is already lifted in the paramagnetic phase of EuCd$_2$As$_2$. We attribute this effect to the itinerant electrons experiencing quasistatic and quasi-long-range ferromagnetic fluctuations. Moreover, the spin nondegenerate band structure harbors a pair of ideal Weyl nodes near the Fermi level. Hence, we show that long-range magnetic order and the spontaneous breaking of time-reversal symmetry are not an essential requirement for WSM states in centrosymmetric systems, and that WSM states can emerge in a wider range of condensed-matter systems than previously thought.

cond-mat.str-el

Superconductivity in SrTiO$_{3}$: dielectric function method for non-parabolic bands

The dielectric function method for superconductivity has been applied to SrTiO$_{3}$ accounting for the non-parabolic dispersion of charge carriers in the conduction band and for the dispersion of optical phonons based on density functional theory calculations. The obtained critical temperatures of the superconducting phase transition in SrTiO$_{3}$ are in agreement with experiments in the density range $n\sim5\times10^{18}$ to $5\times10^{20}$ cm$^{-3}$. The dielectric function method predicts also the sign of the anomalous isotope effect in strontium titanate, in line with recent observations.

cond-mat.supr-con

Parametrization of LSDA+$U$ for noncollinear magnetic configurations: Multipolar magnetism in UO$_2$

To explore the formation of noncollinear magnetic configurations in materials with strongly correlated electrons, we derive a noncollinear LSDA+$U$ model involving only one parameter $U$, as opposed to the difference between the Hubbard and Stoner parameters $U-J$. Computing $U$ in the constrained random phase approximation, we investigate noncollinear magnetism of uranium dioxide UO$_2$ and find that the spin-orbit coupling (SOC) stabilizes the 3$\textbf{k}$ ordered magnetic ground state. The estimated SOC strength in UO$_2$ is as large as 0.73 eV per uranium atom, making spin and orbital degrees of freedom virtually inseparable. Using a multipolar pseudospin Hamiltonian, we show how octupolar and dipole-dipole exchange coupling help establish the 3$\textbf{k}$ magnetic ground state with canted ordering of uranium $f$-orbitals. The cooperative Jahn-Teller effect does not appear to play a significant part in stabilizing the noncollinear 3$\textbf{k}$ state, which has the lowest energy even in an undistorted lattice. The choice of parameter $U$ in the LSDA+$U$ model has a notable quantitative effect on the predicted properties of UO$_2$, in particular on the magnetic exchange interaction and, perhaps trivially, on the band gap: The value of $U=3.46$ eV computed fully $ab$ $initio$ delivers the band gap of 2.11~eV in good agreement with experiment, and a balanced account of other pertinent energy scales.

cond-mat.str-el

Diagrammatic Monte Carlo study of the Fr\"ohlich polaron dispersion in 2D and 3D

We present results for the solution of the large polaron Fr\"ohlich Hamiltonian in 3-dimensions (3D) and 2-dimensions (2D) obtained via the Diagrammatic Monte Carlo (DMC) method. Our implementation is based on the approach by Mishchenko [A.S. Mishchenko et al., Phys. Rev. B 62, 6317 (2000)]. Polaron ground state energies and effective polaron masses are successfully benchmarked with data obtained using Feynman's path integral formalism. By comparing 3D and 2D data, we verify the analytically exact scaling relations for energies and effective masses from 3D$\to$2D, which provides a stringent test for the quality of DMC predictions. The accuracy of our results is further proven by providing values for the exactly known coefficients in weak- and strong coupling expansions. Moreover, we compute polaron dispersion curves which are validated with analytically known lower and upper limits in the small coupling regime and verify the first order expansion results for larger couplings, thus disproving previous critiques on the apparent incompatibility of DMC with analytical results and furnishing useful reference for a wide range of coupling strengths.

cond-mat.mtrl-sci

Three-Dimensional Electronic Structure of type-II Weyl Semimetal WTe$_2$

By combining bulk sensitive soft-X-ray angular-resolved photoemission spectroscopy and accurate first-principles calculations we explored the bulk electronic properties of WTe$_2$, a candidate type-II Weyl semimetal featuring a large non-saturating magnetoresistance. Despite the layered geometry suggesting a two-dimensional electronic structure, we find a three-dimensional electronic dispersion. We report an evident band dispersion in the reciprocal direction perpendicular to the layers, implying that electrons can also travel coherently when crossing from one layer to the other. The measured Fermi surface is characterized by two well-separated electron and hole pockets at either side of the $\Gamma$ point, differently from previous more surface sensitive ARPES experiments that additionally found a significant quasiparticle weight at the zone center. Moreover, we observe a significant sensitivity of the bulk electronic structure of WTe$_2$ around the Fermi level to electronic correlations and renormalizations due to self-energy effects, previously neglected in first-principles descriptions.

cond-mat.mtrl-sci

Ru-doping on iron based pnictides: the "unfolded" dominant role of structural effects for superconductivity

We present an ab-initio study of Ru substitution in two different compounds, BaFe2As2 and LaFeAsO, pure and F-doped. Despite the many similarities among them, Ru substitution has very different effects on these compounds. By means of an unfolding technique, which allows us to trace back the electronic states into the primitive cell of the pure compounds, we are able to disentangle the effects brought by the local structural deformations and by the impurity potential to the states at the Fermi level. Our results are compared with available experiments and show: i) satisfying agreement of the calculated electronic properties with experiments, confirming the presence of a magnetic order on a short range scale; ii) Fermi surfaces strongly dependent on the internal structural parameters, more than on the impurity potential. These results enter a widely discussed field in the literature and provide a better understanding of the role of Ru in iron pnictides: although isovalent to Fe, the Ru-Fe substitution leads to changes in the band structure at the Fermi level mainly related to local structural modifications.

cond-mat.supr-con

Dual behavior of excess electrons in rutile TiO2

The behavior of electrons in the conduction band of TiO2 and other transition-metal oxides is key to the many applications of these materials. Experiments seem to produce conflicting results: optical and spin-resonance techniques reveal strongly localized small polarons, while electrical measurements show high mobilities that can only be explained by delocalized free electrons. By means of hybrid functional calculations we resolve this apparent contradiction and show that small polarons can actually coexist with delocalized electrons in the conduction band of TiO2, the former being energetically only slightly more favorable. We also find that small polarons can form complexes with oxygen vacancies and ionized shallow-donor impurities, explaining the rich spectrum of Ti$^{3+}$ species observed in electron spin resonance experiments.

cond-mat.mtrl-sci

Exceptionally large room-temperature ferroelectric polarization in the novel PbNiO3 multiferroic oxide

We present a study based on several advanced First-Principles methods, of the recently synthesized PbNiO3 [J. Am. Chem. Soc 133, 16920 (2011)], a rhombohedral antiferromagnetic insulator which crystallizes in the highly distorted R3c crystal structure. We find this compound electrically polarized, with a very large electric polarization of about 100 (\muC/cm)^2, thus even exceeding the polarization of well-known BiFeO3. PbNiO3 is a proper ferroelectric, with polarization driven by large Pb-O polar displacements along the [111] direction. Contrarily to naive expectations, a definite ionic charge of 4+ for Pb ion can not be assigned, and in fact the large Pb 6s-O 2p hybridization drives the ferroelectric distortion through a lone-pair mechanism similar to that of other Pb- and Bi-based multiferroics

cond-mat.str-el

Structural transitions and transport-half-metallic ferromagnetism in LaMnO3 at elevated pressure

By means of hybrid density functional theory we investigate the evolution of the structural, electronic and magnetic properties of the colossal magnetoresistance (CMR) parent compound LaMnO$_3$ under pressure. We predict a transition from a low pressure antiferromagnetic (AFM) insulator to a high pressure ferromagnetic (FM) transport half-metal (tHM), characterized by a large spin polarization (~ 80-90 %). The FM-tHM transition is associated with a progressive quenching of the cooperative Jahn-Teller (JT) distortions which transform the $Pnma$ orthorhombic phase into a perfect cubic one (through a mixed phase in which JT-distorted and regular MnO6 octahedra coexist), and with a high-spin (S=2, m_Mn=3.7 mu_B) to low-spin (S=1, m_Mn=1.7 mu_B) magnetic moment collapse. These results interpret the progression of the experimentally observed non-Mott metalization process and open up the possibility of realizing CMR behaviors in a stoichiometric manganite.

cond-mat.str-el

Maximally localized Wannier functions in LaMnO3 within PBE+U, hybrid functionals, and partially self-consistent GW: an efficient route to construct ab-initio tight-binding parameters for e_g perovskites

Using the newly developed VASP2WANNIER90 interface we have constructed maximally localized Wannier functions (MLWFs) for the e_g states of the prototypical Jahn-Teller magnetic perovskite LaMnO3 at different levels of approximation for the exchange-correlation kernel. These include conventional density functional theory (DFT) with and without additional on-site Hubbard U term, hybrid-DFT, and partially self-consistent GW. By suitably mapping the MLWFs onto an effective e_g tight-binding (TB) Hamiltonian we have computed a complete set of TB parameters which should serve as guidance for more elaborate treatments of correlation effects in effective Hamiltonian-based approaches. The method-dependent changes of the calculated TB parameters and their interplay with the electron-electron (el-el) interaction term are discussed and interpreted. We discuss two alternative model parameterizations: one in which the effects of the el-el interaction are implicitly incorporated in the otherwise "noninteracting" TB parameters, and a second where we include an explicit mean-field el-el interaction term in the TB Hamiltonian. Both models yield a set of tabulated TB parameters which provide the band dispersion in excellent agreement with the underlying ab initio and MLWF bands.

cond-mat.str-el

Exchange interactions and magnetic phases of transition metal oxides: benchmarking advanced ab initio methods

The magnetic properties of the transition metal monoxides MnO and NiO are investigated at equilibrium and under pressure via several advanced first-principles methods coupled with Heisenberg Hamiltonian MonteCarlo. The comparative first-principles analysis involves two promising beyond-local density functionals approaches, namely the hybrid density functional theory and the recently developed variational pseudo-self-interaction correction method, implemented with both plane-wave and atomic-orbital basis sets. The advanced functionals deliver a very satisfying rendition, curing the main drawbacks of the local functionals and improving over many other previous theoretical predictions. Furthermore, and most importantly, they convincingly demonstrate a degree of internal consistency, despite differences emerging due to methodological details (e.g. plane waves vs. atomic orbitals)

cond-mat.str-el

Exceptionally strong magnetism in 4d perovskites RTcO3 (R=Ca,Sr,Ba)

The evolution of the magnetic ordering temperature of the 4d3 perovskites RTcO3 (R=Ca,Sr,Ba) and its relation with its electronic and structural properties has been studied by means of hybrid density functional theory and Monte Carlo simulations. When compared to the most widely studied 3d perovskites the large spatial extent of the 4d shells and their relatively strong hybridization with oxygen weaken the tendency to form Jahn-Teller like orbital ordering. This strengthens the superexchange interaction. The resulting insulating G-type antiferromagnetic ground state is characterized by large superexchange coupling constants (26-35 meV) and Neel temperatures (750-1200 K). These monotonically increase as a function of the R ionic radius due to the progressive enhancement of the volume and the associated decrease of the cooperative rotation of the TcO6 octahedra.

cond-mat.str-el

Polymeric forms of carbon in dense lithium carbide

The immense interest in carbon nanomaterials continues to stimulate intense research activities aimed to realize carbon nanowires, since linear chains of carbon atoms are expected to display novel and technologically relevant optical, electrical and mechanical properties. Although various allotropes of carbon (e.g., diamond, nanotubes, graphene, etc.) are among the best known materials, it remains challenging to stabilize carbon in the one-dimensional form because of the difficulty to suitably saturate the dangling bonds of carbon. Here, we show through first-principles calculations that ordered polymeric carbon chains can be stabilized in solid Li$_2$C$_2$ under moderate pressure. This pressure-induced phase (above 5 GPa) consists of parallel arrays of twofold zigzag carbon chains embedded in lithium cages, which display a metallic character due to the formation of partially occupied carbon lone-pair states in \emph{sp}$^2$-like hybrids. It is found that this phase remains the most favorable one in a wide range of pressure. At extreme pressure (larger the 215 GPa) a structural and electronic phase transition towards an insulating single-bonded threefold-coordinated carbon network is predicted.

cond-mat.mtrl-sci