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V. Pardo

Publications and source records attributed to V. Pardo.

At least 37 records · Page 2Linked to original sources

Tuning the thermoelectric properties of SrTiO3 by controlled oxygen doping

We report the thermoelectric properties (Seebeck coefficient, thermal conductivity, and electrical resistivity) of lightly doped single crystals of (001)-oriented SrTiO3 (STO). Hall effect measurements show that electron doping around 10^-5 carriers per unit cell can be achieved by vacuum annealing of the crystals under carefully controlled conditions. The steep density of states near the Fermi energy of STO at this doping level (confirmed by ab initio calculations) retains an unusually large Seebeck coefficient, in spite of an increase in the electronic conductivity by several orders of magnitude. This effect, combined with a decrease in thermal conductivity due to vacancy disorder scattering makes intrinsic doping in STO (and other materials) an alternative strategy to optimize its thermoelectric figure of merit.

cond-mat.str-el↗

Ab initio study of the influence of nanoscale doping inhomogeneities in the phase separated state of La$_{1-x}$Ca$_{x}$MnO$_3$

The chemical influence in the phase separation phenomenon that occurs in perovskite manganites is discussed by means of ab initio calculations. Supercells have been used to simulate a phase separated state, that occurs at Ca concentrations close to the localized to itinerant crossover. We have first considered a model with two types of magnetic ordering coexisting within the same compound. This is not stable. However, a non-isotropic distribution of chemical dopants is found to be the ground state. This leads to regions in the system with different effective concentrations, that would always accompany the magnetic phase separation at the same nanometric scale, with hole-rich regions being more ferromagnetic in character and hole-poor regions being in the antiferromagnetic region of the phase diagram, as long as the system is close to a phase crossover.

cond-mat.str-el↗

Electronic structure of CrN: A comparison between different exchange correlation potentials

We report a series of electronic structure calculations for CrN using different exchange correlation potentials: PBE, LDA+$U$, the Tran-Blaha modified Becke-Johnson, and hybrid functionals. In every case, our calculations show that the onset of magnetism in CrN should be accompanied by a gap opening. The experimentally found antiferromagnetic order always leads to an insulating behavior. Our results give further evidence that the Tran-Blaha functional is very useful for treating the electronic structure of correlated semiconductors allowing a parameter free description of the system. Hybrid functionals are also well capable of describing the electronic structure of CrN. The analysis of the system is complemented with our calculations of the thermopower that are in agreement with the experimental data.

cond-mat.str-el↗

Linear bands, zero-momentum Weyl semimetal, and topological transition in skutterudite-structure pnictides

It was reported earlier [Phys. Rev. Lett. 106, 056401 (2011)] that the skutterudite structure compound CoSb$_3$ displays a unique band structure with a topological transition versus a symmetry-preserving sublattice (Sb) displacement very near the structural ground state. The transition is through a massless Dirac-Weyl semimetal, point Fermi surface phase which is unique in that (1) it appears in a three dimensional crystal, (2) the band critical point occurs at $k$=0, and (3) linear bands are degenerate with conventional (massive) bands at the critical point (before inclusion of spin-orbit coupling). Further interest arises because the critical point separates a conventional (trivial) phase from a topological phase. In the native cubic structure this is a zero-gap topological semimetal; we show how spin-orbit coupling and uniaxial strain converts the system to a topological insulator (TI). We also analyze the origin of the linear band in this class of materials, which is the characteristic that makes them potentially useful in thermoelectric applications or possibly as transparent conductors. We characterize the formal charge as Co$^{+}$ $d^8$, consistent with the gap, with its $\bar{3}$ site symmetry, and with its lack of moment. The Sb states are characterized as $p_x$ (separately, $p_y$) $σ$-bonded $Sb_4$ ring states occupied and the corresponding antibonding states empty. The remaining (locally) $p_z$ orbitals form molecular orbitals with definite parity centered on the empty $2a$ site in the skutterudite structure. Eight such orbitals must be occupied; the one giving the linear band is an odd orbital singlet $A_{2u}$ at the zone center. We observe that the provocative linearity of the band within the gap is a consequence of the aforementioned near-degeneracy, which is also responsible for the small band gap.

cond-mat.mtrl-sci↗

Electronic structure of V$_4$O$_7$: charge ordering, metal-insulator transition and magnetism

The low and high-temperature phases of V$_4$O$_7$ have been studied by \textit{ab initio} calculations. At high temperature, all V atoms are electronically equivalent and the material is metallic. Charge and orbital ordering, associated with the distortions in the V pseudo-rutile chains, occur below the metal-insulator transition. Orbital ordering in the low-temperature phase, different in V$^{3+}$ and V$^{4+}$ chains, allows to explain the distortion pattern in the insulating phase of V$_4$O$_7$. The in-chain magnetic couplings in the low-temperature phase turn out to be antiferromagnetic, but very different in the various V$^{4+}$ and V$^{3+}$ bonds. The V$^{4+}$ dimers formed below the transition temperature form spin singlets, but V$^{3+}$ ions, despite dimerization, apparently participate in magnetic ordering.

cond-mat.str-el↗

Sr$_6$Co$_5$0{$_1$$_5$}: non-one-dimensional behavior of a charge ordered structurally quasi-one-dimensional oxide

We have synthesized Sr$_6$Co$_5$O$_{15}$, a quasi-one-dimensional oxide, measured its magnetic properties and calculated its electronic structure by ab initio techniques. We have found strong evidence for its electronic and magnetic behavior not to follow the trend of its structural series. The magnetic coupling inside the CoO$_3$ chains is not purely ferromagnetic, the long-range coupling inside them is very weak. The Co moments are slightly canted due to their large orbital angular momenta being oriented along each particular quantization axis, that is different for each Co$^{4+}$ atom in the structure. Our thermopower calculations are in agreement with the experiment, supporting our model of the magnetic ground state of the compound.

cond-mat.str-el↗

CdV2O4: A rare example of a collinear multiferroic spinel

By studying the dielectric properties of the geometrically frustrated spinel CdV2O4, we observe ferroelectricity developing at the transition into the collinear antiferromagnetic ground state. In this multiferroic spinel, ferroelectricity is driven by local magnetostriction and not by the more common scenario of spiral magnetism. The experimental findings are corroborated by ab-initio calculations of the electric polarization and the underlying spin and orbital order. The results point towards a charge rearrangement due to dimerization, where electronic correlations and the proximity to the insulator-metal transition play an important role.

cond-mat.str-el↗

Dirac Point Degenerate with Massive Bands at a Topological Quantum Critical Point

The quasi-linear bands in the topologically trivial skutterudite insulator CoSb$_3$ are studied under adiabatic, symmetry-conserving displacement of the Sb sublattice. In this cubic, time-reversal and inversion symmetric system, a transition from trivial insulator to topological point Fermi surface system occurs through a critical point in which massless (Dirac) bands are {\it degenerate} with massive bands. Spin-orbit coupling does not alter the character of the transition. The mineral skutterudite (CoSb$_3$) is very near the critical point in its natural state.

cond-mat.str-el↗

Fermiology and transport properties of the half-metallic itinerant ferromagnet CoS$_2$: influence of spin orbit coupling

Electronic structure calculations were performed on the compound CoS$_2$, an itinerant ferromagnet whose magnetic properties can be understood in terms of spin fluctuation theory. We have identified nesting features in the Fermi surface of the compound, active for long wavelength spin fluctuations. The electronic structure of the material is close to a half-metal. We show the importance of introducing spin-orbit coupling (SOC) in the calculations, that partially destroys the half-metallicity of the material. By means of transport properties calculations, we have quantified the influence of SOC in the conductivity at room temperature, with an important decrease comparing to the GGA alone conductivity. SOC also helps to understand the negative 0 of the material, whose conductivity varies by a few percent with the introduction of small perturbations in the states around the Fermi level.

cond-mat.str-el↗

Tight-binding modeling and low-energy behavior of the semi-Dirac point

We develop a tight-binding model description of semi-Dirac electronic spectra, with highly anisotropic dispersion around point Fermi surfaces, recently discovered in electronic structure calculations of VO$_2$/TiO$_2$ nano-heterostructures. We contrast their spectral properties with the well known Dirac points on the honeycomb lattice relevant to graphene layers and the spectra of bands touching each other in zero-gap semiconductors. We also consider the lowest order dispersion around one of the semi-Dirac points and calculate the resulting electronic energy levels in an external magnetic field. We find that these systems support apparently similar electronic structures but diverse low-energy physics.

cond-mat.str-el↗

Study of the pressure effects in TiOCl by ab initio calculations

Electronic structure calculations on the low dimensional spin-1/2 compound TiOCl were performed at several pressures in the orthorhombic phase, finding that the structure is quasi-one-dimensional. The Ti3+ (d1) ions have one t2g orbital occupied (dyz) with a large hopping integral along the b direction of the crystal. The most important magnetic coupling is Ti-Ti along the b axis. The transition temperature (Tc) has a linear evolution with pressure, and at about 10 GPa this Tc is close to room temperature, leading to a room temperature spin-Peierls insulator-insulator transition, with an important reduction of the charge gap in agreement with the experiment. On the high-pressure monoclinic phase, TiOCl presents two possible dimerized structures, with a long or short dimerization. Long dimerized state occurs above 15 GPa, and below this pressure the short dimerized structure is the more stable phase.

cond-mat.str-el↗

Magnetism Driven by Anion Vacancies in Superconducting $α$--FeSe$_{1-x}$

To study the microscopic electronic and magnetic interactions in the substoichiometric iron chalcogenide FeSe$_{1-x}$ which is observed to superconduct at x~1/8 up to $T_c$=27 K, we use first principles methods to study the Se vacancy in this nearly magnetic FeSe system. The vacancy forms a ferrimagnetic cluster of eight Fe atoms, which for the ordered x=1/8 alloy leads to half metallic conduction. Similar magnetic clusters are obtained for FeTe$_{1-x}$ and for BaFe$_2$As$_2$ with an As vacancy, although neither of these are half metallic. Based on fixed spin density results, we suggest the low energy excitations in FeSe$_{1-x}$ are antiparamagnon-like with short correlation length.

cond-mat.supr-con↗

Magnetism from $2p$ States in Alkaline Earth Monoxides: Trends with Varying N Impurity Concentration

$2p$-based magnetic moments and magnetic coupling are studied with density functional based methods for substitutional N in the alkaline earth monoxide series MgO, CaO, SrO, BaO. The hole is rather strongly localized near the N$^{2-}$ ion, being somewhat more so when strong on-site interactions are included in the calculations. Strong magnetic coupling is obtained in the itinerant electron limit but decreases strongly in the localized limit in which the Coulomb repulsion within the N $2p$ shell (U) is much greater than the N $2p$ impurity bandwidth (W). We find that this limit is appropriate for realistic N concentrations. Ordering on a simple cubic sublattice may maximize the magnetic coupling due to its high directionality.

cond-mat.str-el↗

Identification of a Marginal Fermi-Liquid in Itinerant Ferromagnet CoS2

We report specific heat, resistivity and susceptibility measurements at different temperatures, magnetic fields, and pressures to provide solid evidence of CoS2 being a marginal Fermi liquid. The presence of a tricritical point in the phase diagram of the system provides an opportunity to test the spin fluctuation theory with a high limit of accuracy. A magnetic field suppresses the amplitude of the spin fluctuations and recovers conventional Fermi liquid behavior, connecting both states continuously.

cond-mat.str-el↗

Enhanced dimerization of TiOCl under pressure: spin-Peierls - to - Peierls transition

We report high-pressure x-ray diffraction and magnetization measurements combined with ab-initio calculations to demonstrate that the high-pressure optical and transport transitions recently reported in TiOCl, correspond in fact to an enhanced Ti3+-Ti3+ dimerization existing already at room temperature. Our results confirm the formation of a metal-metal bond between Ti3+ ions along the b-axis of TiOCl, accompanied by a strong reduction of the electronic gap. The evolution of the dimerization with pressure suggests a crossover from the spin-Peierls to a conventional Peierls situation at high pressures.

cond-mat.str-el↗

Homopolar bond formation in ZnV$_2$O$_4$ close to a metal-insulator transition

Electronic structure calculations for spinel vanadate ZnV$_2$O$_4$ show that partial electronic delocalization in this system leads to structural instabilities. These are a consequence of the proximity to the itinerant-electron boundary, not being related to orbital ordering. We discuss how this mechanism naturally couples charge and lattice degrees of freedom in magnetic insulators close to such a crossover. For the case of ZnV$_2$O$_4$, this leads to the formation of V-V dimers along the [011] and [101] directions that readily accounts for the intriguing magnetic structure of ZnV$_2$O$_4$.

cond-mat.str-el↗

Enhanced Pressure Dependence of Magnetic Exchange in A2+[V2]O4 Spinels Approaching the Itinerant Electron Limit

We report a systematic enhancement of the pressure dependence of TN in A2+[V2]O4 spinels as the V-V separation approaches the critical separation for a transition to itinerant-electron behavior. An intermediate phase between localized and itinerant electron behavior is identified in Zn[V2]O4 and Mg[V2]O4 exhibiting mobile holes as large polarons. In Zn[V2]O4, cooperative ordering of V-V pairs below a Ts=TN does not totally suppress the V3+-ion spins at ambient pressure, but makes TN to decrease with pressure. Our results demonstrate that Zn[V2]O4 and Mg[V2]O4 are less localized than previously thought.

cond-mat.str-el↗