SearcharxivSearch

arXiv subjects

D. D. Khalyavin

Publications and source records attributed to D. D. Khalyavin.

At least 19 recordsLinked to original sources

Kagome lattice candidate URhSn: Measured Bragg diffraction patterns and theory for hexagonal and trigonal Sohncke phases

Ternary intermetallics use a ZrNiAl-type chemical structure known as a kagome system. Complexity observed in the phase diagrams of these compounds is attributed to the geometric frustration. The 5f-electron compound URhSn exhibits two phase transitions at 16 K and 54 K. No super-lattice reflections in neutron powder diffraction patterns are detected in the intermediate range of temperatures (16 K - 54 K). Recent resonant x-ray diffraction patterns for uranium ions in the intermediate phase suggest a chiral structure and a trigonal Sohncke space group. It is firmly established that a simple hexagonal space group describes the parent structure at room temperature. A ferroic order parameter that includes hexadecapoles is shown to characterize the trigonal Sohncke phase. Resonant x-ray diffraction by this phase is fully investigated with our symmetry informed theory. It repairs symmetry in the original data analysis by using a grey group, and it lifts an unjustified spatial condition on uranium positions. The theory uses axial atomic multipoles that satisfy sum-rules established in the first instance for x-ray dichroic signals. A confrontation between observed and calculated diffraction patterns lends support to a trigonal Sohncke phase, and exposes grounds for additional experimental work on an enigmatic compound.

cond-mat.str-el

Magnetic structure of diamond EuTi2Al20

We study magnetic symmetries of EuTi2Al20 that appear in the ordering of Eu ions below a temperature at 3.3 K, according to an analysis of substantial experimental evidence [M. Kawamata et al., J. Phys. Soc. Japan. 95, 024701 (2026)]. They descend from the cubic diamond structure that depends explicitly on mixing of orbitals with different spatial parities, e.g., diamond s- and p-atomic states. The lattice (2, 2, 2) Bragg spot, for example, is lattice forbidden in the absence of parity mixing. Our work is motivated by a first proposal that low-temperature magnetic symmetries of diamond EuTi2Al20 are orthorhombic and belong to magnetic crystal classes that include time reversal. Body-centre anti-translation in diffraction patterns is a corollary. Current experimental data does not distinguish between two orthorhombic candidates, even though one is centrosymmetric and the other one is polar. We demonstrate that magnetic parity-odd entities (multipoles) formed by mixing d-and f-atomic states at europium positions, with discreet symmetries that match those of a Dirac monopole, are different for the two candidates. Moreover, the multipoles are visible in resonant x-ray diffraction patterns. The selection rule from parity mixing in the parent cubic diamond structure is preserved, and permitted Bragg spots are different for the two candidate magnetic symmetries. Our symmetry informed diffraction patterns include rotation of the crystal about the reflection vector (an azimuthal angle scan) and a full account of x-ray polarization to spur more revealing experiments.

cond-mat.str-el

Strong impact of low-level substitution of Mn by Fe on the magnetoelectric coupling in $TbMnO_{3}$

The correlation between static magnetoelectric coupling and magnetic structure was investigated in $TbMn_{0.98}Fe_{0.02}O_{3}$ with magnetic field up to 8 T and down to 2 K. Single-crystal neutron diffraction experiments reveal a substantial increase in the temperature dependence of the incommensurate modulation wave vector of the antiferromagnetic phase as the magnetic field strength increases. Magnetic field-dependent pyroelectric current measurements revealed significantly higher magnetoelectric coupling at magnetic fields below 4 T than in pure TbMnO3. This is due to the higher sensitivity of the incommensurably modulated cycloid structure to weak magnetic fields. Detailed analysis of our data confirmed that the ferroelectric polarization is induced by inverse Dzyaloshinskii-Moriya interaction for magnetic field strength up to 4 T, but at higher fields a departure from theoretical predictions is ascertained, giving evidence for an additional, as yet misunderstood, contribution to magnetoelectric coupling. It shows that a small 2% substitution of Mn3+ by Fe3+ has a strong impact on the magnetic structure, promoting the destabilization of the incommensurably modulated magnetic cycloidal structure of $TbMnO_{3}$ in a magnetic field above 5 T. We demonstrate that the magnetoelectric coupling magnitude can be tuned through suitable substitutional elements, even at low level, inducing local lattice distortions with different electronic and magnetic properties.

cond-mat.mtrl-sci

Magnetic properties of the zigzag ladder compound SrTb2O4

We report on the properties of SrTb2O4, a frustrated zigzag ladder antiferromagnet, studied by single crystal neutron diffraction (with polarised neutrons in zero field and unpolarised neutrons in an applied magnetic field), as well as by neutron spectroscopy on a polycrystalline sample. The neutron scattering results are supported by single crystal magnetisation and heat capacity measurements. In zero field, neutron diffraction data show no transition to a magnetically ordered state down to the lowest experimentally available temperature of 35 mK, and the material remains magnetically disordered down to this temperature. Polarised neutron diffraction measurements reveal the presence of a diffuse scattering signal suggesting only very weak spin-spin correlations in the ground state. For H // c (the easy magnetisation direction), we followed the magnetisation process using neutron diffraction measurements and observed the appearance of field-induced magnetic Bragg peaks with integer h and k indices in the (hk0) scattering plane. No magnetic peaks with a non-zero propagation vector were detected. The observed in-field data fit well to a simple two-sublattice model with magnetic moments aligned along the field direction but being significantly different in magnitude for the two inequivalent Tb3+ sites in the unit cell. Overall, the collected data point to a nonmagnetic ground state in SrTb2O4 despite the presence of strong interactions.

cond-mat.str-el

Competing charge and magnetic order in the candidate centrosymmetric skyrmion host EuGa$_2$Al$_2$

Eu(Ga$_{1-x}$Al$_x$)$_4$ are centrosymmetric systems that have recently been identified as candidates to stabilise topologically non-trivial magnetic phases, such as skyrmion lattices. In this Letter, we present a high-resolution resonant x-ray and neutron scattering study on EuAl2Ga2 that provides new details of the complex coupling between the electronic ordering phenomena. Our results unambiguously demonstrate that the system orders to form a spin density wave with moments aligned perpendicular to the direction of the propagation vector, and upon further cooling, a cycloid with moments in the ab plane, in contrast to what has been reported in the literature. We show that concomitant with the onset of the spin density wave is the suppression of the charge order, indicative of a coupling between the localised 4$f$ electrons and itinerant electron density. Furthermore we demonstrate that the charge density wave order breaks the four-fold symmetry present in the I4/mmm crystal structure, thus declassifying these systems as square-net magnets.

cond-mat.str-el

Spontaneous spin chirality reversal and competing phases in the topological magnet EuAl$_4$

We demonstrate the spontaneous reversal of spin chirality in a single crystal sample of the intermetallic magnet EuAl$_4$. We solve the nanoscopic nature of each of the four magnetically phases of EuAl$_4$ using resonant magnetic x-ray scattering, and demonstrate all four phases order with single-k incommensurate magnetic modulation vectors. Below 15.4 K the system forms a spin density modulated spin structure where the spins are orientated in the ab plane perpendicular to the orientation of the magnetic propagation vector. Below 13.2 K a second spin density wave orders with moments aligned parallel to the c-axis, such that the two spin density wave orders coexist. Below 12.2 K a magnetic helix of a single chirality is stabilised across the entire sample. Below 10 K the chirality of the magnetic helix reverses, and the sample remains a single chiral domain. Concomitant with the establishment of the helical magnetic ordering is the lowering of the crystal symmetry to monoclinic, as evidenced the formation of uniaxial charge and spin strip domains. A group theoretical analysis demonstrates that below 12.2 K the symmetry lowers to polar monoclinic, which is necessary to explain the observed asymmetry in the chiral states of the magnetic helix and the spin chiral reversal. We find that in every magnetically ordered phase of EuAl4 the in-plane moment is perpendicular to the orientation of the magnetic propagation vector, which we demonstrate is favoured by magnetic dipolar interactions.

cond-mat.str-el

Polarity vs Chirality: Functionality from competing magneto-structural instabilities

We report a phenomenological magneto-structural model based on competing free-energy terms that couple either polar or chiral distortions in cubic quadruple perovskites, depending on the global direction of magnetic moments. The model naturally explains why some compounds in this material system host magnetically-induced ferroelectricity at low temperature, while others such as CaMn$_3$(Cr$_3$Mn)O$_{12}$, which we characterise experimentally, do not. Importantly, our results suggest a new approach towards developing an applied multiferroic functionality, and can be generalised to other multi-sublattice systems where the magnetic interaction between sublattices is prohibited by spatial inversion.

cond-mat.mtrl-sci

Unusual magnetism of the axion-insulator candidate Eu$_5$In$_2$Sb$_6$

Eu$_5$In$_2$Sb$_6$ is a member of a family of orthorhombic nonsymmorphic rare-earth intermetallics that combines large localized magnetic moments and itinerant exchange with a low carrier density and perpendicular glide planes. This may result in special topological crystalline (wallpaper fermion) or axion insulating phases. Recent studies of Eu$_5$In$_2$Sb$_6$ single crystals have revealed colossal negative magnetoresistance and multiple magnetic phase transitions. Here, we clarify this ordering process using neutron scattering, resonant elastic X-ray scattering, muon spin-rotation, and magnetometry. The nonsymmorphic and multisite character of Eu$_5$In$_2$Sb$_6$ results in coplanar noncollinear magnetic structure with an Ising-like net magnetization along the $a$ axis. A reordering transition, attributable to competing ferro- and antiferromagnetic couplings, manifests as the onset of a second commensurate Fourier component. In the absence of spatially resolved probes, the experimental evidence for this low-temperature state can be interpreted either as an unusual double-$q$ structure or in a phase separation scenario. The net magnetization produces variable anisotropic hysteretic effects which also couple to charge transport. The implied potential for functional domain physics and topological transport suggests that this structural family may be a promising platform to implement concepts of topological antiferromagnetic spintronics.

cond-mat.str-el

Negative Magnetization and Magnetic Ordering of Rare Earth and Transition Metal Sublattices in NdFe0.5Cr0.5O3

We investigate the effect of alloying at the 3d transition metal site of a rare-earth-transition metal oxide, by considering NdFe0.5Cr0.5O3 alloy with two equal and random distribution of 3d ions, Cr and Fe, interacting with an early 4f rare earth ion, Nd. Employing temperature- and field-dependent magnetization measurements, temperature-dependent x-ray diffraction, neutron powder diffraction, and Raman spectroscopy, we characterize its structural and magnetic properties. Our study reveals bipolar magnetic switching (arising from negative magnetization) and magnetocaloric effect which underline the potential of the studied alloy in device application. The neutron diffraction study shows the absence of spin reorientation transition over the entire temperature range of 1.5-320 K, although both parent compounds exhibit spin orientation transition. We discuss the microscopic origin of this curious behavior. The neutron diffraction results also reveal the ordering of Nd spins at an unusually high temperature of about 40 K, which is corroborated by Raman measurements.

cond-mat.mtrl-sci

Magnetic structure, excitations and field induced transitions in the honeycomb lattice $\rm{Er_2Si_2O_7}$

We investigate the magnetic properties of the monoclinic D-type $\rm{Er_2Si_2O_7}$ with a distorted honeycomb lattice using powder and single crystal neutron scattering techniques, as well as single crystal magnetisation measurements. The powder neutron diffraction shows that below the ordering temperature, $T_{\rm N}=1.85$ K, the compound forms a ${\bf q}=0$ antiferromagnetic structure with four sublattices. For $H \! \parallel \! a$, magnetisation measurements reveal a narrow, but clearly visible plateau at one third of the magnetisation saturation value. The plateau's stabilisation is accompanied by a significant increase of the magnetic unit cell, as the magnetic peaks with fractional indices are observed in single crystal neutron diffraction experiments. At low-temperatures, the inelastic neutron scattering measurements reveal the presence of low-energy dispersionless excitations. Their spectrum is sensitive to the applied field, it significantly softens on the magnetisation plateau, and demonstrates the behaviour expected for a non-collinear Ising antiferromagnet away from the plateau.

cond-mat.str-el

Incommensurate antiferromagnetism in UTe2 under pressure

The discovery of multiple superconducting phases in UTe2 boosted research on correlated-electron physics. This heavy-fermion paramagnet was rapidly identified as a reference compound to study the interplay between magnetism and unconventional superconductivity with multiple degrees of freedom. The proximity to a ferromagnetic quantum phase transition was initially proposed as a driving force to triplet-pairing superconductivity. However, we find here that long-range incommensurate antiferromagnetic order is established under pressure. The propagation vector km = (0.07,0.33,1) of the antiferromagnetic phase is close to a wavevector where antiferromagnetic fluctuations have previously been observed at ambient pressure. These elements support that UTe2 is a nearly-antiferromagnet at ambient pressure. Our work appeals for theories modelling the evolution of the magnetic interactions and electronic properties, driving a correlated paramagnetic regime at ambient pressure to a long-range antiferromagnetic order under pressure. A deeper understanding of itinerant-f-electrons magnetism in UTe2 will be a key for describing its unconventional superconducting phases.

cond-mat.str-el

Strain control of a bandwidth-driven spin reorientation in Ca$_{3}$Ru$_{2}$O$_{7}$

The layered-ruthenate family of materials possess an intricate interplay of structural, electronic and magnetic degrees of freedom that yields a plethora of delicately balanced ground states. This is exemplified by Ca$_{3}$Ru$_{2}$O$_{7}$, which hosts a coupled transition in which the lattice parameters jump, the Fermi surface partially gaps and the spins undergo a $90^{\circ}$ in-plane reorientation. Here, we show how the transition is driven by a lattice strain that tunes the electronic bandwidth. We apply uniaxial stress to single crystals of Ca$_{3}$Ru$_{2}$O$_{7}$, using neutron and resonant x-ray scattering to simultaneously probe the structural and magnetic responses. These measurements demonstrate that the transition can be driven by externally induced strain, stimulating the development of a theoretical model in which an internal strain is generated self-consistently to lower the electronic energy. We understand the strain to act by modifying tilts and rotations of the RuO$_{6}$ octahedra, which directly influences the nearest-neighbour hopping. Our results offer a blueprint for uncovering the driving force behind coupled phase transitions, as well as a route to controlling them.

cond-mat.str-el

Templates for magnetic symmetry and altermagnetism in hexagonal MnTe

The symmetry of long-range magnetic order in manganese telluride (alpha-MnTe) is unknown. Likewise, its standing as an altermagnet. To improve the situation, we present symmetry informed Bragg diffraction patterns based on a primary magnetic order parameter for antiferromagnetic alignment between Mn dipoles. It does not break translation symmetry in a centrosymmetric structure, in keeping with an accepted definition of altermagnetism. Our templates serve x-ray diffraction that benefits from signal enhancement using a Mn atomic resonance, and neutron scattering. Even rank multipoles in magnetic neutron diffraction reflect a core requirement of altermagnetism, because they are zero for strong spin-orbit coupling. Symmetry in the templates demands that nuclear and magnetic contributions possess the same phase, which enables standard neutron polarization analysis on Bragg spots with overlapping contributions. However, three of the four templates generate Bragg spots that do not appear in the lattice (nuclear) diffraction pattern, i.e., Bragg spots that are basis-forbidden and purely magnetic in origin. On the other hand, identical symmetry demands a 90 deg phase shift between magnetic (time-odd) and charge-like (time-even, Templeton-Templeton) contributions to x-ray scattering amplitudes. Consequently, circular polarization in the primary beam of x-rays is rotated. The difference in the intensities of a Bragg spot measured with right- and left-handed circular primary polarization defines a chiral signature. Further tests include predictions in three out four templates of zero intensity in a specified channel of x-ray polarization. Diffraction properties of a template are radically different from those of a parity-time (PT)-symmetric antiferromagnet, for its symmetry allows a linear ME effect and prohibits both a PM effect and a chiral signature.

cond-mat.str-el

Spin-density-wave order controlled by uniaxial stress in CeAuSb$_2$

The tetragonal heavy-fermion compound CeAuSb$_2$ (space group $P4/nmm$) exhibits incommensurate spin density wave (SDW) order below $T_{N}\approx6.5~K$ with the propagation vector $\mathbf{q}_A = (δ_A,δ_A,1/2)$. The application of uniaxial stress along the [010] direction induces a sudden change in the resistivity ratio $ρ_a/ρ_b$ at a compressive strain of $ε\approx -0.5$\%. Here we use neutron scattering to show that the uniaxial stress induces a first-order transition to a SDW state with a different propagation vector $(0,δ_B,1/2)$ with $δ_B=0.25$. The magnetic structure of the new (B) phase consists of Ce layers with ordered moments alternating with layers with zero moment stacked along the $c$-axis. The ordered layers have an up-up-down-down configuration along the $b$-axis. This is an unusual situation in which the loss of spatial inversion is driven by the magnetic order. We argue that the change in SDW wavevector leads to Fermi surface reconstruction and a concomitant change in the transport properties.

cond-mat.str-el

The crystal and magnetic structure of cesium superoxide

CsO2 is a member of the family of alkali superoxides (formula AO2 with A= Na, K, Rb and Cs) that exhibit magnetic behavior arising from open $p$-shell electrons residing on O2- molecules. We use neutron diffraction to solve the crystal and magnetic structures of CsO2, and observe a complex series of structures on cooling from room temperature to 1.6 K. These include an incommensurate modulation along the a-axis of the structure at intermediate temperatures, which then locks into a commensurate modulation that doubles the unit cell compared to the previously supposed orthorhombic unit cell. In both incommensurate and commensurate phases our structural solution involves a staggering of the cesium ion positions along the b-axis, in contrast to studies of other alkali superoxides in which staggered tilts of the O2- dimers relative to the c-axis are seen. Below T ~ 10 K we observe magnetic Bragg reflections arising from an antiferromagnetically ordered structure with a wavevector of k = (0,0,0) (relative to the doubled crystallographic unit cell), with moments that point predominantly along the b-axis with a small component along the a-axis that hints at possible anisotropic exchange coupling (consistent with the crystal structure). Measurements of the magnetic Bragg reflections in an applied magnetic field suggest a spin-flop transition takes place between 2 T and 4 T in which moments likely flop to point along the crystallographic a-axis. Our measurements indicate that CsO2 is an interesting example of magnetic properties being inherently linked to the crystal structure, in that the staggered displacement of the cesium ions activates antisymmetric exchange which then permits the observed spin canting.

cond-mat.str-el

The Double-$Q$ Ground State with Topological Charge Stripes in the Skyrmion Candidate $\text{GdRu}_{\text{2}}\text{Si}_{\text{2}}$

$\text{GdRu}_{\text{2}}\text{Si}_{\text{2}}$ is a centrosymmetric magnet in which a skyrmion lattice has recently been discovered. Here, we investigate the magnetic structure of the zero field ground state using neutron diffraction on single crystal and polycrystalline $^{\text{160}}\text{GdRu}_{\text{2}}\text{Si}_{\text{2}}$. In addition to observing the principal propagation vectors $\mathbf{q}_{1}$ and $\mathbf{q}_{2}$, we discover higher order magnetic satellites, notably $\mathbf{q}_{1} + 2\mathbf{q}_{2}$. The appearance of these satellites are explained within the framework of a new double-$Q$ constant-moment solution. Using powder diffraction we implement a quantitative refinement of this model. This structure, which contains vortexlike motifs, is shown to have a one-dimensional topological charge density.

cond-mat.str-el

A magnetic structure of ruthenium dioxide (RuO2) and altermagnetism

The magnetic structure of RuO2 and the Ru atomic configuration are unknown. A magnetic structure is inferred by confronting measured and calculated Bragg diffraction patterns and adjusting the latter to achieve satisfactory agreement. An accepted pattern, a magnetic symmetry, includes symmetry of sites occupied by the magnetic ions. As a realistic starting point, we provide diffraction patterns for a magnetic symmetry of RuO2, a descendent of the tetragonal parent structure, which accommodates a departure of Ru axial dipoles from the crystal c axis. A chiral signal and piezomagnetic effect are permitted, and a linear magnetoelectric effect forbidden. Features of the neutron diffraction pattern test the non-relativistic requirement of altermagnetism, and we scrutinize published room-temperature data. Specifically, one Bragg point is consistent with Ru orbital angular momentum and magnetic quadrupole both zero, and the latter result is not expected from non-relativistic altermagnetism. Azimuthal angle scans in resonant x-ray diffraction are sensitive to the Ru site symmetry and the atomic configuration. Acid tests of the studied magnetic symmetry include a chiral signature and null intensity for unrotated photon polarization.

cond-mat.str-el

Magnetic inhomogeneities in the quadruple perovskite manganite [Y$_{2-x}$Mn$_x$]MnMnMn$_4$O$_{12}$

A combination of competing exchange interactions and substitutional disorder gives rise to magnetic inhomogeneities in the [Y$_{2-x}$Mn$_x$]MnMnMn$_4$O$_{12}$ $x = 0.23$ and $x = 0.16$ quadruple perovskite manganites. Our neutron powder scattering measurements show that both the $x = 0.23$ and $x = 0.16$ samples separate into two distinct magnetic phases; below T$_{1}$ = 120 $\pm$ 10 K the system undergoes a transition from a paramagnetic phase to a phase characterised by short range antiferromagnetic clusters contained in a paramagnetic matrix, and below T$_{2}$ $\sim$ 65 K, the system is composed of well correlated long range collinear ferrimagnetic order, punctuated by short range antiferromagnetic clusters. A sharp increase in the antiferromagnetic phase fraction is observed below $\sim$ 33 K, concomitant with a decrease in the ferrimagnetic phase fraction. Our results demonstrate that the theoretically proposed AFM phase is stabilised in the [Y$_{2-x}$Mn$_x$]MnMnMn$_4$O$_{12}$ manganites in the presence of dominant B-B exchange interactions, as predicted.

cond-mat.str-el