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A. Hadj-Azzem

Publications and source records attributed to A. Hadj-Azzem.

15 recordsLinked to original sources

Origin of the magnetic ground state of Tb$_{2}$Ir$_{2}$O$_{7}$

Magnetic-rare-earth pyrochlore iridates exhibit a rich variety of unconventional phases, driven by the complex interactions within and between the rare-earth and the iridium sublattices. In this study, we investigate the peculiar magnetic state of Tb$_{2}$Ir$_{2}$O$_{7}$, where a component of the Tb$^{3+}$ moment orders perpendicular to its local Ising anisotropy axis. By means of neutron diffraction and inelastic neutron scattering down to dilution temperatures, complemented by specific heat measurements, we show that this intriguing magnetic state is fully established at 1.5 K and we characterize its excitation spectrum across a broad range of energies. Our calculations reveal that bilinear interactions between Tb$^{3+}$ ions subjected to the Ir molecular field capture several key features of the experiments, but need to be supplemented to fully reproduce the observed behavior.

cond-mat.str-el

Ferromagnetic fragmented state in the pyrochlore Ho$_2$Ru$_2$O$_7$

The consecutive magnetic ordering of the Ho and Ru ions in the pyrochlore Ho2Ru2O7 and their interplay are investigated by neutron scattering, magnetic and specific heat measurements. The Ru moments order at 95 K into a $Γ_5$ easy-plane antiferromagnetic state. At 1.55 K the Ho moments order into an unusual $Γ_9$ ferromagnetic state with extensive ground state entropy and structured spin dynamics. It is shown how the internal fields with $Γ_5$ and $Γ_9$ geometry allow for two symmetry breaking transitions. The lower temperature ordering is driven by ruthenium mediated interactions between holmium moments as spin ice correlations develop. The unsaturated order is compatible with a fragmented ferromagnetic state equivalent to pyrochlore kagome ice.

cond-mat.str-el

Slow Oscillations of the Transverse Magnetoresistance in HoTe3

Slow oscillations of the magnetoresistance periodic in the inverse magnetic field with a frequency of 3.4 T have been identified in HoTe3. The temperature dependence of the oscillation amplitude is close to exponential even at low temperatures. This may be attributed to the existence of soft modes in the system and allows the estimation of the electron scattering rate on these modes. In the region of magnetic fields exceeding 1 T, the oscillations can be described as interference oscillations associated with the splitting of the band structure due to the bilayer structure of HoTe3. The obtained data have allowed us to calculate the ratio tb/tz~7.7 of the hopping integrals between layers within each bilayer (tb) and between the adjacent bilayers (tz) to estimate these integrals as tb ~ 2 meV and tz ~ 0.26 meV.

cond-mat.str-el

Magnetic imaging under high pressure with a spin-based quantum sensor integrated in a van der Waals heterostructure

Pressure is a powerful thermodynamic parameter for tuning the magnetic properties of van der Waals magnets owing to their weak interlayer bonding. However, local magnetometry measurements under high pressure still remain elusive for this important class of emerging materials. Here we introduce a method enabling in situ magnetic imaging of van der Waals magnets under high pressure with sub-micron spatial resolution. Our approach relies on a quantum sensing platform based on boron-vacancy (V$_\text{B}^-$) centers in hexagonal boron nitride (hBN), which can be placed in atomic contact of any type of two-dimensional (2D) material within a van der Waals heterostructure. We first show that the V$_\text{B}^-$ center can be used as a magnetic field sensor up to pressures of a few GPa, a pressure range for which the properties of a wide variety of van der Waals magnets are efficiently altered. We then use V$_\text{B}^-$ centers in a thin hBN layer to perform magnetic imaging of a van der Waals magnet under pressure. As a proof of concept, we study the pressure-dependent magnetization in micrometer-sized flakes of $1T$-CrTe$_2$, whose evolution is explained by a shift of the Curie temperature. Besides providing a new path for studying pressure-induced phase transitions in van der Waals magnets, this work also opens up interesting perspectives for exploring the physics of 2D superconductors under pressure via local measurements of the Meissner effect.

cond-mat.mtrl-sci

Comparative study of magnetic quantum oscillations in Hall and transverse magnetoresistance

Magnetic quantum oscillations (MQO) of Hall coefficient are measured in rare-earth tritelluride TmTe$_{3}$ and shown to be much stronger and persist to higher temperature than the Shubnikov oscillations. It is general for MQO in strongly anisotropic metals, and the combined measurements of Hall and diagonal magnetoresistance provide useful informations about the electronic structure. The ratio of their MQO amplitudes depends linearly on magnetic field, and its slope gives a simple and accurate measurement tool of the electron mean free time and its temperature dependence.

cond-mat.str-el

Collective magnetic state induced by charge disorder in the non-Kramers rare-earth pyrochlore Tb$_{2}$ScNbO$_{7}$

Geometrical frustration, as in pyrochlore lattices made of corner-sharing tetrahedra, precludes the onset of conventional magnetic ordering, enabling the stabilization of fluctuating spin states at low temperature. Disorder is a subtle ingredient that can modify the nature of these exotic non-ordered phases. Here, we study the interplay between disorder and magnetic frustration in the new pyrochlore Tb$_{2}$ScNbO$_{7}$ where the non magnetic site presents a charge disorder Nb$^{5+}$/Sc$^{3+}$. Its quantification with sophisticated diffraction techniques (electrons, X-rays, neutrons) allows us to estimate the distribution of the splitting of the magnetic Tb$^{3+}$ non-Kramers ground state doublets and to compare it with excitations measured in inelastic neutron scattering. Combining macroscopic and neutron scattering measurements, we show that a clear spin glass transition at 1 K stems out while retaining strong spin liquid correlations. Our results suggest that Tb$_{2}$ScNbO$_{7}$ stabilizes one of the novel disorder induced quantum spin liquid or topological glassy phases recently proposed theoretically.

cond-mat.str-el

Charge-Density-Waves Tuned by Crystal Symmetry

The electronic orders appearing in condensed matter systems are originating from the precise arrangement of atoms constituting the crystal as well as their nature. This teneous relationship can lead to highly different phases in condensed matter, and drive electronic phase transitions. Here, we show that a very slight deformation of the crystal structure of TbTe$_3$ can have a dramatic influence on the electronic order that is stabilized. In particular, we show that the Charge Density Wave (CDW) developping along the $\vec{c}$ axis in the pristine state, switches to an orientation along $\vec{a}$ when the naturally orthorhombic system is turned into a tetragonal system. This is achieved by performing true biaxial mechanical deformation of a TbTe$_3$ sample from 250K to 375K, and by measuring both structural and electronic parameters with x-ray diffraction and transport measurements. We show that this switching transition is driven by the tetragonality parameter $a/c$, and that the transition occurs for $a=c$, with a coexistence region for $0.9985< a/c < 1.002$. The CDW transition temperature $T_c$ is found to have a linear dependence with $a/c$, with no saturation in the deformed states investigated here, while the gap saturates out of the coexistence region. The linear dependence of $T_c$ is accounted for within a tight-binding model. Our results question the relationship between the gap and $T_c$ in RTe$_3$ systems. More generally, our method of applying true biaxial deformation at cryogenic temperatures can be applied to many systems displaying electronic phase transitions, and opens a new route towards the study of coexisting or competing electronic orders in condensed matter.

cond-mat.str-el

Characterization of room-temperature in-plane magnetization in thin flakes of CrTe$_2$ with a single spin magnetometer

We demonstrate room-temperature ferromagnetism with in-plane magnetic anisotropy in thin flakes of the CrTe$_2$ van der Waals ferromagnet. Using quantitative magnetic imaging with a single spin magnetometer based on a nitrogen-vacancy defect in diamond, we infer a room-temperature in-plane magnetization in the range of $M\sim 27$ kA/m for flakes with thicknesses down to $20$ nm. In addition, our measurements indicate that the orientation of the magnetization is not determined solely by shape anisotropy in micron-sized CrTe$_2$ flakes, which suggest the existence of a non-negligible magnetocrystalline anisotropy. These results make CrTe$_2$ a unique system in the growing family of van der Waals ferromagnets, as it is the only material platform known to date which offers an intrinsic in-plane magnetization and a Curie temperature above $300$ K in thin flakes.

cond-mat.mtrl-sci

Kitaev interactions in the Co honeycomb antiferromagnets Na$_3$Co$_2$SbO$_6$ and Na$_2$Co$_2$TeO$_6$

Co$^{2+}$ ions in an octahedral crystal field, stabilise a j$_{eff}$ = 1/2 ground state with an orbital degree of freedom and have been recently put forward for realising Kitaev interactions, a prediction we have tested by investigating spin dynamics in two cobalt honeycomb lattice compounds, Na$_2$Co$_2$TeO$_6$ and Na$_3$Co$_2$SbO$_6$, using inelastic neutron scattering. We used linear spin wave theory to show that the magnetic spectra can be reproduced with a spin Hamiltonian including a dominant Kitaev nearest-neighbour interaction, weaker Heisenberg interactions up to the third neighbour and bond-dependent off-diagonal exchange interactions. Beyond the Kitaev interaction that alone would induce a quantum spin liquid state, the presence of these additional couplings is responsible for the zigzag-type long-range magnetic ordering observed at low temperature in both compounds. These results provide evidence for the realization of Kitaev-type coupling in cobalt-based materials, despite hosting a weaker spin-orbit coupling than their 4d and 5d counterparts.

cond-mat.str-el

Strongly coupled charge, orbital and spin order in TbTe$_{3}$

We report a ground state with strongly coupled magnetic and charge density wave orders mediated via orbital ordering in the layered compound \tbt. In addition to the commensurate antiferromagnetic (AFM) and charge density wave (CDW) orders, new magnetic peaks are observed whose propagation vector equals the sum of the AFM and CDW propagation vectors, revealing an intricate and highly entwined relationship. This is especially interesting given that the magnetic and charge orders lie in different layers of the crystal structure where the highly localized magnetic moments of the Tb$^{3+}$ ions are netted in the Tb-Te stacks, while the charge order is formed by the conduction electrons of the adjacent Te-Te layers. Our results, based on neutron diffraction and resonant x-ray scattering reveal that the charge and magnetic subsystems mutually influence each other via the orbital ordering of Tb$^{3+}$ ions.

cond-mat.str-el

Toward equilibrium ground state of charge density waves in rare-earth tritellurides

We show that the charge density wave (CDW) ground state below the Peierls transition temperature, $T_{CDW}$, of rare-earth tritellurides is not at its equilibrium value, but depends on the time where the system was kept at a fixed temperature below $T_{CDW}$. This ergodicity breaking is revealed by the increase of the threshold electric field for CDW sliding which depends exponentially on time. We tentatively explain this behavior by the reorganization of the oligomeric (Te$_x$)$^{2-}$ sequence forming the CDW modulation.

cond-mat.str-el

Interplay between electron band-anticrossing and charge-density-wave instabilities

Our measurements of the Hall coefficient in rare-earth tritelluride compounds reveal a strong hysteresis between cooling and warming in the low temperature range where a second unidirectional charge density wave (CDW) occurs. We show that this effect results from the interplay between two instabilities: band crossing of the Te $p_{x}$ and $p_{y}$ orbitals at the Fermi level and CDW, which have a close energy gain and compete. Calculation of the electron susceptibility at the CDW wave vector with and without band anticrossing reconstruction of the electron spectrum yields a satisfactory estimation of the temperature range of the hysteresis in Hall effect measurements.

cond-mat.str-el

Magnetic properties of the honeycomb oxide Na$_2$Co$_2$TeO$_6$

We have studied the magnetic properties of Na$_2$Co$_2$TeO$_6$, which features a honeycomb lattice of magnetic Co$^{2+}$ ions, through macroscopic characterization and neutron diffraction on a powder sample. We have shown that this material orders in a zig-zag antiferromagnetic structure. In addition to allowing a linear magnetoelectric coupling, this magnetic arrangement displays very peculiar spatial magnetic correlations, larger in the honeycomb planes than between the planes, which do not evolve with the temperature. We have investigated this behavior by Monte Carlo calculations using the $J_1$-$J_2$-$J_3$ model on a honeycomb lattice with a small interplane interaction. Our model reproduces the experimental neutron structure factor, although its absence of temperature evolution must be due to additional ingredients, such as chemical disorder or quantum fluctuations enhanced by the proximity to a phase boundary.

cond-mat.str-el

Anisotropy tuned magnetic order in pyrochlore iridates

The magnetic behavior of polycrystalline samples of Er$_2$Ir$_2$O$_7$ and Tb$_2$Ir$_2$O$_7$ pyrochlores is studied by magnetization measurements and neutron diffraction. Both compounds undergo a magnetic transition at 140 and 130 K respectively, associated with an ordering of the Ir sublattice, signaled by thermomagnetic hysteresis. In Tb$_2$Ir$_2$O$_7$, we show that the Ir molecular field leads the Tb magnetic moments to order below 40 K in the all-in/all-out magnetic arrangement. No sign of magnetic long range order on the Er sublattice is evidenced in Er$_2$Ir$_2$O$_7$ down to 0.6 K where a spin freezing is detected. These contrasting behaviors result from the competition between the Ir molecular field and the different single-ion anisotropy of the rare-earths on which it is acting. Additionally, this strongly supports the all-in/all-out iridium magnetic order.

cond-mat.str-el

Non-magnetic doping induced magnetism in Li doped SnO2 nanoparticles

We address the possibility of non-magnetic doping induced magnetism, in Li doped SnO2 nano-particles. The compounds have been prepared by solid state route at equilibrium and were found to be crystallized in single rutile phase. The magnetization measurements have shown that Li-doping induces magnetism in SnO2 for a particular range of Li concentration. However, for other Li concentrations, including pure SnO2, the samples exhibit diamagnetism. To investigate the possible origin of the induced magnetism, we have studied the variation of the magnetization as a function of the average nano-particle radius. Possible scenarios for the appearance of magnetism in these compounds are discussed.

cond-mat.mtrl-sci