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Andres Cano

Publications and source records attributed to Andres Cano.

13 recordsLinked to original sources

Electron vs. hole doping in infinite-layer nickelates: electronic structure, magnetism and correlations

The observation of superconductivity in undoped infinite-layer nickelates $R$NiO$_2$ ($R$ = rare earth) challenges our current understanding and calls for a re-examination of the underlying electronic structure of this family of materials. In this context, it is particularly important to extend the investigation of $R$NiO$_2$ compounds from the intensively studied hole-doped regime to the almost unexplored electron-doped one. Here, we use a combination of density-functional theory and dynamical mean-field theory to study the evolution of the electronic structure of infinite-layer nickelates in these two doping regimes. We find a striking asymmetry in the self-doping of the Ni-$d_{x^2-y^2}$ band due to the $R(5d)$ states: while this effect is strongly suppressed upon hole doping, electron doping instead leads to an increase in the size of the $R(5d)$ electron pockets, but without effectively hole-doping the Ni-$d_{x^2-y^2}$ band. This asymmetry has an important impact on the magnetic response as antiferromagnetism is rapidly suppressed upon hole doping, whereas it remains the ground state upon electron doping. Despite these differences, electronic correlations on both sides of the phase diagram are dominated by the Ni $d_{x^2-y^2}$ orbital, suggesting that a single-band description may be appropriate for infinite-layer nickelates in both the electron- and hole-doped regimes.

cond-mat.str-el

(Anti-)Altermagnetism from Orbital Ordering in the Ruddlesden-Popper Chromates Sr$_{n+1}$Cr$_n$O$_{3n+1}$

Altermagnets are collinear antiferromagnets with spin-split electronic states. We introduce Ruddlesden-Popper chromates Sr$_{n+1}$Cr$_n$O$_{3n+1}$ (including SrCrO$_3$) as candidate materials in which altermagnetism can emerge from spontaneous orbital ordering rather than crystal symmetry. First-principles calculations reveal a layer-dependent spin splitting: if the spin and orbital orders align in adjacent layers, the system exhibits non-relativistic spin splitting, and thus altermagnetism. In contrast, if either the spin or the orbital order is reversed in adjacent layers, we observe a layerwise uncompensated spin splitting, that is compensated in the adjacent layer, giving rise to the concept of anti-altermagnetism. In the RP series, odd $n$ members support coexistence of altermagnetism and anti-altermagnetism, whereas even $n$ and the perovskite limit are strictly anti-altermagnetic. In both cases, larger $n$ favors metallicity, and in odd $n$ compounds strain can further stabilize altermagnetism.

cond-mat.mtrl-sci

Lattice dynamics in the FeSi-based family of superconductors

The lattice dynamics of the superconducting materials LaFeSiH and LaFeSiO as well as their intermetallic precursor LaFeSi are investigated by polarized Raman spectroscopy and first-principles calculations, together with X-ray and advanced electron diffraction techniques for their structural analysis. We find that the Fe-dominated Raman-active modes reflect the chemical peculiarities of these silicides compared to their pnictide counterparts, with enhanced structural couplings between the FeSi layer and the spacer that can be related to the ionic vs covalent character of the latter. In addition, we find signatures of enhanced electron-phonon coupling for some of the Raman-active modes. Beyond that, our study reveals intriguing Fe-based Raman features as well as structural subtleties in LaFeSiH suggesting that this superconductor may formally be non-centrosymmetric.

cond-mat.supr-con

The third dimension of ferroelectric domain walls

Ferroelectric domain walls are quasi-2D systems that show great promise for the development of non-volatile memory, memristor technology and electronic components with ultra-small feature size. Electric fields, for example, can change the domain wall orientation relative to the spontaneous polarization and switch between resistive and conductive states, controlling the electrical current. Being embedded in a 3D material, however, the domain walls are not perfectly flat and can form networks, which leads to complex physical structures. We demonstrate the importance of the nanoscale structure for the emergent transport properties, studying electronic conduction in the 3D network of neutral and charged domain walls in ErMnO$_3$. By combining tomographic microscopy techniques and finite element modelling, we clarify the contribution of domain walls within the bulk and show the significance of curvature effects for the local conduction down to the nanoscale. The findings provide insights into the propagation of electrical currents in domain wall networks, reveal additional degrees of freedom for their control, and provide quantitative guidelines for the design of domain wall based technology.

cond-mat.mtrl-sci

Multiferroic Quantum Criticality

The zero-temperature limit of a continuous phase transition is marked by a quantum critical point, which can generate exotic physics that extends to elevated temperatures. Magnetic quantum criticality is now well known, and has been explored in systems ranging from heavy fermion metals to quantum Ising materials. Ferroelectric quantum critical behaviour has also been recently established, motivating a flurry of research investigating its consequences. Here, we introduce the concept of multiferroic quantum criticality, in which both magnetic and ferroelectric quantum criticality occur in the same system. We develop the phenomenology of multiferroic quantum critical behaviour, describe the associated experimental signatures, and propose material systems and schemes to realize it.

cond-mat.mtrl-sci

Frequency dependent polarisation switching in h-ErMnO$_3$

We report an electric-field poling study of the geometric-driven improper ferroelectric h-ErMnO$_3$. From a detailed dielectric analysis we deduce the temperature and frequency dependent range for which single-crystalline h-ErMnO$_3$ exhibits purely intrinsic dielectric behaviour, i.e., free from extrinsic so-called Maxwell-Wagner polarisations that arise, for example, from surface barrier layers. In this regime ferroelectric hysteresis loops as function of frequency, temperature and applied electric fields are measured revealing the theoretically predicted saturation polarisation in the order of 5 - 6 $μ$C/cm$^2$. Special emphasis is put on frequency-dependent polarisation switching, which is explained in terms of domain-wall movement similar to proper ferroelectrics. Controlling the domain walls via electric fields brings us an important step closer to their utilization in domain-wall-based electronics.

cond-mat.mtrl-sci

First-principles study of (Ba,Ca)TiO$_3$ and Ba(Ti,Zr)O$_3$ solid solutions

(Ba,Ca)TiO$_3$ and Ba(Ti,Zr)O$_3$ solid solutions are the building blocks of lead-free piezoelectric materials that attract a renewed interest. We investigate the properties of these systems by means of first-principles calculations, with a focus on the lattice dynamics and the competition between different ferroelectric phases. We first analyze the four parent compounds in order to compare their properties and their different tendency towards ferroelectricity. The core of our study is systematic characterization of the binary systems (Ba,Ca)TiO$_3$ and Ba(Ti,Zr)O$_3$ within both the Virtual Crystal Approximation and direct supercell calculations. In the case of Ca doping, we find a gradual transformation from $A$-site to $B$-site ferroelectricity due to steric effects that largely determines the behavior of the system. In the case of Zr doping, in contrast, the behavior is eventually dominated by cooperative Zr-Ti motions and the local electrostatics. In addition, our comparative study reveals that the specific microscopic physics of these solid sets severe limits to the applicability of the Virtual Crystal Approximation for these systems.

cond-mat.mtrl-sci

Helical bunching and symmetry lowering inducing multiferroicity in Fe langasites

The chiral Fe-based langasites represent model systems of triangle-based frustrated magnets with a strong potential for multiferroicity. We report neutron scattering measurements for the multichiral Ba3MFe3Si2O14 (M = Nb, Ta) langasites revealing new important features of the magnetic order of these systems: the bunching of the helical modulation along the c-axis and the in-plane distortion of the 120{\textdegree} Fe-spin arrangement. We discuss these subtle features in terms of the microscopic spin Hamiltonian, and provide the link to the magnetically-induced electric polarization observed in these systems. Thus, our findings put the multiferroicity of this attractive family of materials on solid ground.

cond-mat.str-el

Iron-based superconductors: Foreword

We introduce the thematic (open access) issue published in Comptes Rendus Physique. This issue is focused on the so-called Fe-based superconductors that, since the discovery of superconductivity in F-doped LaFeAsO by Hosono group in 2008, have become one of the latest hot topics in the field of condensed matter. The idea is to give an up-to-date overview of the fundamental properties of this novel family of high-Tc superconductors. First we briefly recall the scientific context of superconductivity and its relationship to magnetism in metallic compounds, and then we detail the specific aspects of Fe-based superconductors addressed in the issue.

cond-mat.str-el

Helical order and multiferroicity in the $S=1/2$ quasi-kagome system KCu$_3$As$_2$O$_7$(OD)$_3$

Several Cu$^{2+}$ hydroxide minerals have recently been identified as candidate realizations of the $S=1/2$ kagome Heisenberg model. In this context, we have studied the distorted system KCu$_3$As$_2$O$_7$(OD)$_3$ using neutron scattering and bulk measurements. Although the distortion favors magnetic order over a spin liquid ground state, refinement of the magnetic diffraction pattern below $T_{N1}=7.05(5)$ K yields a complex helical structure with $\mathbf{k}=(0.77~0~0.11)$. This structure, as well as the spin excitation spectrum, are well described by a classical Heisenberg model with ferromagnetic nearest neighbor couplings. Multiferroicity is observed below $T_{N1}$, with an unusual crossover between improper and pseudo-proper behavior occurring at $T_{N2}=5.5$ K. The polarization at $T=2$ K is $P=1.5 μ$Cm$^{-2}$. The properties of KCu$_3$As$_2$O$_7$(OD)$_3$ highlight the variety of physics which arise from the interplay of spin and orbital degrees of freedom in Cu$^{2+}$ kagome systems.

cond-mat.str-el

Magneto- to electro-active transmutation of spin waves in ErMnO3

The low energy dynamical properties of the multiferroic hexagonal perovskite ErMnO3 have been studied by inelastic neutron scattering as well as terahertz and far infrared spectroscopies on synchrotron source. From these complementary techniques, we have determined the magnon and crystal field spectra and identified a zone center magnon only excitable by the electric field of an electromagnetic wave. Using comparison with the isostructural YMnO3 compound and crystal field calculations, we propose that this dynamical magnetoelectric process is due to the hybridization of a magnon with an electro-active crystal field transition.

cond-mat.str-el

THz Magneto-electric atomic rotations in the chiral compound Ba$_3$NbFe$_3$Si$_2$O$_{14}$

We have determined the terahertz spectrum of the chiral langasite Ba$_3$NbFe$_3$Si$_2$O$_{14}$ by means of synchrotron-radiation measurements. Two excitations are revealed that are shown to have a different nature. The first one, purely magnetic, is observed at low temperature in the magnetically ordered phase and is assigned to a magnon. The second one persits far into the paramagnetic phase and exhibits both an electric and a magnetic activity at slightly different energies. This magnetoelectric excitation is interpreted in terms of atomic rotations and requires a helical electric polarization.

cond-mat.str-el

Anisotropic conductance at improper ferroelectric domain walls

Transition metal oxides hold great potential for the development of new device paradigms because of the field-tunable functionalities driven by their strong electronic correlations, combined with their earth abundance and environmental friendliness. Recently, the interfaces between transition-metal oxides have revealed striking phenomena such as insulator-metal transitions, magnetism, magnetoresistance, and superconductivity. Such oxide interfaces are usually produced by sophisticated layer-by-layer growth techniques, which can yield high quality, epitaxial interfaces with almost monolayer control of atomic positions. The resulting interfaces, however, are fixed in space by the arrangement of the atoms. Here we demonstrate a route to overcoming this geometric limitation. We show that the electrical conductance at the interfacial ferroelectric domain walls in hexagonal ErMnO3 is a continuous function of the domain wall orientation, with a range of an order of magnitude. We explain the observed behaviour using first-principles density functional and phenomenological theories, and relate it to the unexpected stability of head-to-head and tail-to-tail domain walls in ErMnO3 and related hexagonal manganites. Since the domain wall orientation in ferroelectrics is tunable using modest external electric fields, our finding opens a degree of freedom that is not accessible to spatially fixed interfaces.

cond-mat.str-el