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Showing papers on "Magnetic structure published in 2016"


Journal ArticleDOI
TL;DR: This work identifies two distinct mechanisms that contribute to θSHeff: the first mechanism, which is facet-independent, arises from conventional bulk spin-dependent scattering within the IrMn3 layer, and the second intrinsic mechanism is derived from the unconventional antiferromagnetic structure of IrN3.
Abstract: There has been considerable interest in spin-orbit torques for the purpose of manipulating the magnetization of ferromagnetic elements for spintronic technologies. Spin-orbit torques are derived from spin currents created from charge currents in materials with significant spin-orbit coupling that propagate into an adjacent ferromagnetic material. A key challenge is to identify materials that exhibit large spin Hall angles, that is, efficient charge-to-spin current conversion. Using spin torque ferromagnetic resonance, we report the observation of a giant spin Hall angle θ SH eff of up to ~0.35 in (001)-oriented single-crystalline antiferromagnetic IrMn 3 thin films, coupled to ferromagnetic permalloy layers, and a θ SH eff that is about three times smaller in (111)-oriented films. For (001)-oriented samples, we show that the magnitude of θ SH eff can be significantly changed by manipulating the populations of various antiferromagnetic domains through perpendicular field annealing. We identify two distinct mechanisms that contribute to θ SH eff : the first mechanism, which is facet-independent, arises from conventional bulk spin-dependent scattering within the IrMn 3 layer, and the second intrinsic mechanism is derived from the unconventional antiferromagnetic structure of IrMn 3 . Using ab initio calculations, we show that the triangular magnetic structure of IrMn 3 gives rise to a substantial intrinsic spin Hall conductivity that is much larger for the (001) than for the (111) orientation, consistent with our experimental findings.

212 citations


Journal ArticleDOI
TL;DR: In this paper, the magnetic structure and magnon dynamics of FePS3, an S = 2 Ising-like quasi-two-dimensional antiferromagnet with a honeycomb lattice, were determined.
Abstract: Neutron scattering from single crystals has been used to determine the magnetic structure and magnon dynamics of FePS3, an S = 2 Ising-like quasi-two-dimensional antiferromagnet with a honeycomb lattice. The magnetic structure has been confirmed to have a magnetic propagation vector of k(M) = [01 1/2] and the moments are collinear with the normal to the ab planes. The magnon data could be modeled using a Heisenberg Hamiltonian with a single-ion anisotropy. Magnetic interactions up to the third in-plane nearest neighbor needed to be included for a suitable fit. The best fit parameters for the in-plane exchange interactions were J(1) = 1.46, J(2) = -0.04, and J(3) = -0.96 meV. The single-ion anisotropy is large, Delta = 2.66 meV, explaining the Ising-like behavior of the magnetism in the compound. The interlayer exchange is very small, J' = -0.0073 meV, proving that FePS3 is a very good approximation to a two-dimensional magnet.

128 citations



Journal ArticleDOI
15 Nov 2016
TL;DR: In this paper, the ferromagnetic layers of Fe3GeTe2 were determined to order antiferromagnetically along the c-axis below 152 K and the ground state was further substantiated by theoretical calculation.
Abstract: Fe3GeTe2 is known as an air-stable layered metal with itinerant ferromagnetism with a transition temperature of about 220 K. From our extensive dc and ac magnetic measurements, we have determined that the ferromagnetic layers of Fe3GeTe2 actually order antiferromagnetically along the c-axis below 152 K. The antiferromagnetic state was further substantiated by theoretical calculation to be the ground state. A magnetic structure model was proposed to describe the antiferromagnetic ground state as well as competition between antiferromagnetic and ferromagnetic states. Fe3GeTe2 shares many common features with pnictide superconductors and may be a promising system in which to search for unconventional superconductivity.

114 citations


Journal ArticleDOI
TL;DR: In this paper, the BaFe11.9In0.1O19 polycrystalline sample has been performed in a wide temperature range from 10 K up to 730 K and in the magnetic fields up to 14 T.

114 citations


Journal ArticleDOI
TL;DR: In this paper, the crystal and magnetic structures of the BaFe12−xAlxO19 (x = 0.1−1.2) solid solutions have been investigated with powder neutron diffractometry.
Abstract: The investigations of the crystal and magnetic structures of the BaFe12−xAlxO19 (x = 0.1–1.2) solid solutions have been performed with powder neutron diffractometry. Magnetic properties of the BaFe12−xAlxO19 (x = 0.1–1.2) solid solutions have been measured by vibration sample magnetometry at different temperatures under different magnetic fields. The atomic coordinates and lattice parameters have been Rietveld refined. The invar effect is observed in low temperature range (from 4.2 K to 150 K). It is explained by the thermal oscillation anharmonicity of atoms. The increase of microstress with decreasing temperature is found from Rietveld refinement. The Curie temperature and the change of total magnetic moment per formula unit are found for all compositions of the BaFe12−xAlxO19 (x = 0.1–1.2) solid solutions. The magnetic structure model is proposed. The most likely reasons and the mechanism of magnetic structure formation are discussed.

95 citations


Journal ArticleDOI
TL;DR: The orbital magnetism of skyrmions is studied and it is demonstrated that the contribution driven by the emergent magnetic field is topological, which means that the topological contribution to the orbital moment does not change under continuous deformations of the magnetic structure.
Abstract: When electrons are driven through unconventional magnetic structures, such as skyrmions, they experience emergent electromagnetic fields that originate several Hall effects. Independently, ground-state emergent magnetic fields can also lead to orbital magnetism, even without the spin-orbit interaction. The close parallel between the geometric theories of the Hall effects and of the orbital magnetization raises the question: does a skyrmion display topological orbital magnetism? Here we first address the smallest systems with nonvanishing emergent magnetic field, trimers, characterizing the orbital magnetic properties from first-principles. Armed with this understanding, we study the orbital magnetism of skyrmions and demonstrate that the contribution driven by the emergent magnetic field is topological. This means that the topological contribution to the orbital moment does not change under continuous deformations of the magnetic structure. Furthermore, we use it to propose a new experimental protocol for the identification of topological magnetic structures, by soft X-ray spectroscopy.

67 citations


Journal ArticleDOI
TL;DR: A high-pressure NMR study on FeSe single crystals reveals the magnetic phase transition to be first-order type, implying the existence of a concomitant structural transition via a spin-lattice coupling and provides clear evidence for strong coupling between nematicity and magnetism in FeSe.
Abstract: To elucidate the magnetic structure and the origin of the nematicity in FeSe, we perform a high-pressure ^{77}Se NMR study on FeSe single crystals. We find a suppression of the structural transition temperature with pressure up to about 2 GPa from the anisotropy of the Knight shift. Above 2 GPa, a stripe-order antiferromagnetism that breaks the spatial fourfold rotational symmetry is determined by the NMR spectra under different field orientations and with temperatures down to 50 mK. The magnetic phase transition is revealed to be first-order type, implying the existence of a concomitant structural transition via a spin-lattice coupling. Stripe-type spin fluctuations are observed at high temperatures, and remain strong with pressure. These results provide clear evidence for strong coupling between nematicity and magnetism in FeSe, and therefore support a universal scenario of magnetic driven nematicity in iron-based superconductors.

67 citations


Journal ArticleDOI
TL;DR: This work shows that more complex magnetic materials - using the example of the Heusler and half-Heusler alloys - allow for purely optical excitations to cause a significant change in the local moments on the order of 5 fs, and demonstrates that qualitative behaviour of this rich magnetic response to laser light can be deduced from the ground-state spectrum.
Abstract: The overarching goal of the field of femtomagnetism is to control, via laser light, the magnetic structure of matter on a femtosecond time scale. The temporal limits to the light-magnetism interaction are governed by the fact that the electron spin interacts indirectly with light, with current studies showing a laser induced global loss in the magnetic moment on a time scale of the order of a few 100 s of femtoseconds. In this work, by means of ab-initio calculations, we show that more complex magnetic materials - we use the example of the Heusler and half-Heusler alloys - allow for purely optical excitations to cause a significant change in the local moments on the order of 5 fs. This, being purely optical in nature, represents the ultimate mechanism for the short time scale manipulation of spins. Furthermore, we demonstrate that qualitative behaviour of this rich magnetic response to laser light can be deduced from the ground-state spectrum, thus providing a route to tailoring the response of some complex magnetic materials, like the Heuslers, to laser light by the well established methods for material design from ground-state calculations.

66 citations


Journal ArticleDOI
TL;DR: In this article, a hexagonal O3-type structure of Na3Co2SbO6 was shown to have a strong orbital contribution above the expected spin-only value of 3.87 μ B.

65 citations


Journal ArticleDOI
TL;DR: The magnetic structure in Cd2Os2O7 is resolved with neutron diffraction and then via resonant inelastic X-ray scattering determine the salient electronic and magnetic energy scales controlling the MIT.
Abstract: Much consideration has been given to the role of spin-orbit coupling (SOC) in 5d oxides, particularly on the formation of novel electronic states and manifested metal-insulator transitions (MITs). SOC plays a dominant role in 5d5 iridates (Ir4+), undergoing MITs both concurrent (pyrochlores) and separated (perovskites) from the onset of magnetic order. However, the role of SOC for other 5d configurations is less clear. For example, 5d3 (Os5+) systems are expected to have an orbital singlet with reduced effective SOC. The pyrochlore Cd2Os2O7 nonetheless exhibits a MIT entwined with magnetic order phenomenologically similar to pyrochlore iridates. Here, we resolve the magnetic structure in Cd2Os2O7 with neutron diffraction and then via resonant inelastic X-ray scattering determine the salient electronic and magnetic energy scales controlling the MIT. In particular, SOC plays a subtle role in creating the electronic ground state but drives the magnetic order and emergence of a multiple spin-flip magnetic excitation.

Journal ArticleDOI
TL;DR: The ground state of the quantum spin ice candidate magnet Yb2Ti2O7 is known to be sensitive to weak disorder at the similar to 1% level which occurs in single crystals grown from the melt.
Abstract: We know the ground state of the quantum spin ice candidate magnet Yb2Ti2O7 to be sensitive to weak disorder at the similar to 1% level which occurs in single crystals grown from the melt. Powders produced by solid state synthesis tend to be stoichiometric and display large and sharp heat capacity anomalies at relatively high temperatures, T-C similar to 0.26 K. We have carried out neutron elastic and inelastic measurements on well characterized and equilibrated stoichiometric powder samples of Yb2Ti2O7 which show resolution-limited Bragg peaks to appear at low temperatures, but whose onset correlates with temperatures much higher than T-C. The corresponding magnetic structure is best described as an icelike splayed ferromagnet. In the spin dynamics of Yb2Ti2O7 we see the gapless on an energy scale <0.09 meV at all temperatures and organized into a continuum of scattering with vestiges of highly overdamped ferromagnetic spin waves present. These excitations differ greatly from conventional spin waves predicted for Yb2Ti2O7's mean field ordered state, but appear robust to weak disorder as they are largely consistent with those displayed by nonstoichiometric crushed single crystals and single crystals, as well as by powder samples of Yb2Ti2O7's sister quantum magnet Yb2Ti2O7.

Journal ArticleDOI
TL;DR: A baromagnetic effect in a novel tetragonal magnetic structure is introduced by vacancies in Mn3 Ga0.95 N0.94 due to the change of the Mn-Mn distance and their spin re-orientation induced by a pressure field, proven for the first time in antiperovskite compounds by neutron powder diffraction analysis.
Abstract: A baromagnetic effect in a novel tetragonal magnetic structure is introduced by vacancies in Mn3 Ga0.95 N0.94 , due to the change of the Mn-Mn distance and their spin re-orientation induced by a pressure field. This effect is proven for the first time in antiperovskite compounds by neutron powder diffraction analysis. This feature will enable wide applications in magnetoelectric devices and intelligent instruments.

Journal ArticleDOI
TL;DR: In this article, the crystal and magnetic structures of AlFe2B2 have been studied with a combination of X-ray and neutron diffraction and electronic structure calculations, and the magnetic and magnetocaloric properties have been determined.

Journal ArticleDOI
TL;DR: In this paper, the surface and internal magnetic structure of bamboo-like cylindrical nanowires with tailored diameter modulations have been determined exploiting the direct photoemission and transmission contrasts using photo-emission electron microscopy combined with X-ray magnetic circular dichroism, as well as complementary magnetic force microscopy and micromagnetic simulations.
Abstract: The surface and the internal magnetic structure of bamboo-like cylindrical nanowires with tailored diameter modulations have been determined exploiting the direct photoemission and transmission contrasts using photoemission electron microscopy combined with X-ray magnetic circular dichroism, as well as complementary magnetic force microscopy and micromagnetic simulations. Bamboo-like cylindrical nanowires with diameters of 130 and 140 nm, and a modulation periodicity of 400 nm were electrochemically grown into the pores of alumina templates. FeCoCu and Co nanowires were selected to offer parallel and perpendicular magnetization easy axis, respectively. For FeCoCu nanowires, a main longitudinal magnetization configuration is found consistent with the predominant shape anisotropy. In addition, a weaker modulated contrast along the wires’ axis is observed that matches the position of each diameter modulation: vortex-like structures are observed at the ends of the wires and at the surface around the modulations. In Co nanowires, a multi-segmented vortex-like structure with alternating opposite chirality is found not matching the periodicity of the diameter modulations. Such a spin configuration is interpreted considering that Co nanowires exhibit hexagonal symmetry with c axis nearly perpendicular to the nanowires defining strong uniaxial transverse magnetocrystalline anisotropy.

Journal ArticleDOI
TL;DR: In this paper, the magnetic structure of the most active perovskites for the oxygen evolution reaction was studied. But the magnetic properties of the perovs were not investigated.
Abstract: We have performed an in-depth ab initio study of the magnetic structure within the most active perovskites for the oxygen evolution reaction. In all cases, the ground state exhibits an extended antiferromagnetic coupling in the unit cell. Layered antiparallel alignment of the magnetic moments appears to be related to their electrocatalytic activity. All the perovskites calculated within this paper show space-separated charge-transport channels depending on the spin orientation. Comparing the electronic structures with the reported activities, we find a direct correlation between the magnetic accumulation on the spin channels in the bulk material and the catalytic activity. We discuss the possible implications of such observations in terms of magnetic interactions. During oxygen evolution in water electrolysis, reactants and products do not preserve spin. For triplet state oxygen to evolve, the catalyst at the anode can speed up the reaction if it is able to balance the magnetism of the oxygen molecule by extracting electrons with an opposite magnetic moment, conserving the overall spin.

Journal ArticleDOI
27 Jul 2016
TL;DR: In this paper, the authors review neutron measurements of prototypical examples of these different approaches to achieving multiferrocity in TbMnO3 and compare them with single-phase multiferroics.
Abstract: Multiferroics are materials that evince both ferroelectric and magnetic order parameters. These order parameters when coupled can lead to both exciting new physics as well as new device applications. Potential device applications include memory, magnetic field sensors, small antennas and so on. Since Kimura’s discovery of multiferroicity in TbMnO3, there has been a renaissance in the study of these materials. Great progress has been made in both materials discovery and in the theoretical understanding of these materials. In type-II systems the magnetic order breaks the inversion symmetry of the material, driving a secondary ferroelectric phase transition in which the ferroelectric polarisation is exquisitely coupled to the magnetic structure and thus to magnetic field. In type-I systems, the magnetic and ferroelectric orders are established on different sublattices of the material and typically are weakly coupled, but electric field can still drive changes in the magnetisation. Besides single-phase multiferroics, there has been exciting progress in composite heterostructures of multiferroics. Here, we review neutron measurements of prototypical examples of these different approaches to achieving multiferrocity.

Journal ArticleDOI
TL;DR: In this article, the electric field effect on the magnetic domain structure of a Pt/Co system was studied, where an EF was applied to the top surface of the Co layer and the width of the maze domain was significantly modified by the application of the EF at a temperature slightly below the Curie temperature.
Abstract: The electric field (EF) effect on the magnetic domain structure of a Pt/Co system was studied, where an EF was applied to the top surface of the Co layer. The width of the maze domain was significantly modified by the application of the EF at a temperature slightly below the Curie temperature. After a detailed analysis, a change in the microscopic exchange stiffness induced by the EF application was suggested to dominate the modulation of the domain width observed in the experiment. The accumulation of electrons at the surface of the Co layer resulted in an increase in the microscopic exchange stiffness and the Curie temperature. The result was consistent with the recent theoretical prediction.

Journal ArticleDOI
TL;DR: In this paper, the anomalous Hall effect of the ferromagnetic Heusler compound Mn2RhSn has been investigated using sputtering techniques on MgO (001) substrates.
Abstract: Recently non-collinear magnetic structures have attracted renewed attention due to the novel Hall effects that they display. In earlier work evidence for a non-collinear magnetic structure has been reported for the ferromagnetic Heusler compound Mn2RhSn. Using sputtering techniques we have prepared high quality epitaxial thin films of Mn2RhSn by high temperature growth on MgO (001) substrates. The films are tetragonally distorted with an easy magnetization axis along the c-axis. Moreover, we find evidence for an anomalous Hall effect whose magnitude increases strongly below the Curie temperature that is near room temperature. Consistent with theoretical calculations of the anomalous Hall conductivity that we have carried out by deriving the Berry curvature from the electronic structure of perfectly ordered Mn2RhSn, the sign of the anomalous Hall conductivity is negative, although the measured value is considerably smaller than the calculated value. We attribute this difference to small deviations in stoichiometry and chemical ordering. We also find evidence for a topological Hall resistivity of about 50 nΩ cm, which is ~5% of the anomalous Hall effect, for temperatures below 100 K. The topological Hall effect signifies the presence of a chiral magnetic structure that evolves from the non-collinear magnetic structure that Mn2RhSn is known to exhibit.

Journal ArticleDOI
Hasung Sim1, Joosung Oh1, Jaehong Jeong1, Manh Duc Le1, Je-Geun Park1 
TL;DR: In this review it is demonstrated how the use of both neutron and X-ray diffraction and inelastic neutron scattering techniques have been essential to paint this comprehensive and coherent picture of h-RMnO3.
Abstract: The hexagonal RMnO3(h-RMnO3) are multiferroic materials, which exhibit the coexistence of a magnetic order and ferroelectricity. Their distinction is in their geometry that both results in an unusual mechanism to break inversion symmetry and also produces a two-dimensional triangular lattice of Mn spins, which is subject to geometrical magnetic frustration due to the antiferromagnetic interactions between nearest-neighbor Mn ions. This unique combination makes the h-RMnO3 a model system to test ideas of spin-lattice coupling, particularly when both the improper ferroelectricity and the Mn trimerization that appears to determine the symmetry of the magnetic structure arise from the same structure distortion. In this review we demonstrate how the use of both neutron and X-ray diffraction and inelastic neutron scattering techniques have been essential to paint this comprehensive and coherent picture of h-RMnO3.

Journal ArticleDOI
TL;DR: In this article, the perovskite orthoferrite SmFeO3 was synthesized by the hydrothermal method and the Neel temperature of this material was found to be 655 K by temperature-dependent magnetization measurements.

Journal ArticleDOI
TL;DR: In this article, the double perovskite Y${}{2}$CoMnO${}_{6}$ showed spontaneous magnetization and electrical polarization at low temperature.
Abstract: The finding of new multiferroic materials, where electric and magnetic orders coexist, is a challenging task currently. The double perovskite Y${}_{2}$CoMnO${}_{6}$ shows spontaneous magnetization and electrical polarization at low temperature. Previous investigations of this compound did not reach agreement about the type of magnetic structure present. This study demonstrates that this compound exhibits a collinear ferromagnetic ordering of Co${}^{2+}$ and Mn${}^{4+}$ moments in the $a\phantom{\rule{0}{0ex}}c$ plane with a small antiferromagnetic canting along the $b$ axis. A thorough characterization of the dielectric properties reveals the absence of any related anomaly in the dielectric permittivity and the lack of spontaneous electrical polarization ($P$) in the $P$($E$, electric field) loops. The pyroelectric current is strongly dependent on the number of antisite defects in the Co/Mn arrangement, the heating rate, and the poling field. Thus, the observed electric polarization is due to thermally stimulated depolarization currents ascribed to defect dipoles mainly placed at the antiphase boundaries. No ferroelectric transition occurs in this material, disproving the existence of intrinsic magnetoelectric multiferroicity.

Journal ArticleDOI
TL;DR: The analysis of the antioxidant activity and DC conductivity of the NiO samples confirmed the presence of both Ni(2+) and O(2-) vacancies and the dependence of uncompensated moments on total spins contradicts Neel's models and is found to vary directly with O( 2-) vacancy concentration.
Abstract: Nanostructured nickel oxide samples with crystallite sizes in the range 32-45 nm are synthesized through a facile chemical route using nickel chloride and ethanol amine as the starting materials. The analysis of the antioxidant activity and DC conductivity of the NiO samples confirmed the presence of both Ni(2+) and O(2-) vacancies. The temperature dependent magnetization studies of the samples are done using a Vibrating Sample Magnetometer in the range 20-300 K. The core-shell magnetic structure of the NiO nanoparticles with an antiferromagnetic core and a spin-glass shell is revealed from the zero field cooled and field cooled magnetization studies of the samples. The dependence of uncompensated moments on total spins contradicts Neel's models and is found to vary directly with O(2-) vacancy concentration. The ferromagnetic response of NiO samples due to the interaction between the antiferromagnetic core and the ferromagnetic shell is evident from the magnetic hysteresis studies in the temperature range 20-300 K. The ferromagnetic response is traced to the concentration of O(2-) vacancies, which act as donor impurities and mediate the alignment of magnetic moments associated with Ni(2+) vacancies. The decrease of ferromagnetic contribution upon annealing is explained by the decrease in the concentration of O(2-) vacancies which caused a reduction in the number of magnetic polarons and hence the effective magnetization.

Journal ArticleDOI
TL;DR: It is reported that synthetic melanothallite Cu2OCl2, which is the first discovery of multiferroicity in a transition metal oxyhalide, belongs to a new class of magnetoelectricMultiferroic materials with an exceptionally high critical temperature.
Abstract: Magnetoelectric multiferroics have attracted enormous attention in the past years because of their high potential for applications in electronic devices, which arises from the intrinsic coupling between magnetic and ferroelectric ordering parameters. The initial finding in TbMnO3 has triggered the search for other multiferroics with higher ordering temperatures and strong magnetoelectric coupling for applications. To date, spin-driven multiferroicity is found mainly in oxides, as well as in a few halogenides. We report multiferroic properties for synthetic melanothallite Cu2OCl2, which is the first discovery of multiferroicity in a transition metal oxyhalide. Measurements of pyrocurrent and the dielectric constant in Cu2OCl2 reveal ferroelectricity below the Neel temperature of ~70 K. Thus, melanothallite belongs to a new class of multiferroic materials with an exceptionally high critical temperature. Powder neutron diffraction measurements reveal an incommensurate magnetic structure below TN, and all magnetic reflections can be indexed with a propagation vector [0.827(7), 0, 0], thus discarding the claimed pyrochlore-like “all-in–all-out” spin structure for Cu2OCl2, and indicating that this transition metal oxyhalide is, indeed, a spin-induced multiferroic material.

Journal ArticleDOI
TL;DR: In this article, the second transition-metal-only double perovskite, Mn2MnReO6, was reported, which was prepared at high pressure and temperature.
Abstract: Transition-metal-only double perovskite oxides (A2BB′O6) are of great interest due to their strong and unusual magnetic interactions; only one compound, Mn2FeReO6, was reported in this category to date. Herein, we report the second transition-metal-only double perovskite, Mn2MnReO6, prepared at high pressure and temperature. Mn2MnReO6 crystallizes in a monoclinic P21/n structure, as established by synchrotron X-ray and powder neutron diffraction (PND) methods, with eight-coordinated A sites and rock-salt arrangement of the B and B′-site MnO6 and ReO6. Both the structural analysis and the X-ray absorption near edge spectroscopy results indicate mixed valence states of the B/B′-site in Mn2+2Mn2+/3+Re5+/6+O6. The magnetic and PND studies evidence an antiferromagnetic (AFM) transition at ∼110 K and a transition from a simple AFM to canted AFM with net ferromagnetic component at ∼50 K. The observed Efros–Shklovskii variable-range-hopping semiconducting behavior is attributed to the three (A-site Mn2+, B-site M...

Journal ArticleDOI
TL;DR: In this paper, the authors obtained direct insight into unknown aspects of the physics of the iridium ions in pyrochlore iridates via neutron diffraction experiments, which might be caused by the small ordered Ir moment and also by the neutron absorbing properties of the Ir ions.
Abstract: Among others, pyrochlore iridates with strong spin-orbit coupling have received attention recently due to the prediction of Weyl semimetal states in these materials. Despite tremendous efforts, there exists no direct measurement of the spin structure at the iridium site by means of neutron diffraction. This might be caused by the small ordered Ir moment and also by the neutron absorbing properties of the Ir ions. Up to now, only basic indirect evidence for the spin structure at the iridium site exists. From the observation here of the full magnetic structure of Nd${}_{2}$Ir${}_{2}$O${}_{7}$ via neutron diffraction experiments, the authors obtain direct insight into unknown aspects of the physics of the iridium ions in pyrochlore iridates.

Journal ArticleDOI
TL;DR: In this paper, the magnetic domain configuration of a micrometer-thick FeGd multilayer with hard x-ray dichroic ptychography at energies spanning both the Gd ${L}_{3}$ edge and the Fe $K$ edge was analyzed.
Abstract: Imaging the magnetic structure of a material is essential to understanding the influence of the physical and chemical microstructure on its magnetic properties. Magnetic imaging techniques, however, have been unable to probe three-dimensional micrometer-size systems with nanoscale resolution. Here we present the imaging of the magnetic domain configuration of a micrometer-thick FeGd multilayer with hard x-ray dichroic ptychography at energies spanning both the Gd ${L}_{3}$ edge and the Fe $K$ edge, providing a high spatial resolution spectroscopic analysis of the complex x-ray magnetic circular dichroism. With a spatial resolution reaching $45\phantom{\rule{0.28em}{0ex}}\mathrm{nm}$, this advance in hard x-ray magnetic imaging is a first step towards the investigation of buried magnetic structures and extended three-dimensional magnetic systems at the nanoscale.

Journal ArticleDOI
TL;DR: The field-induced phases of URu2Si2 are identified as a spin-density-wave state and the transition to the spin- density wave represents a unique touchstone for understanding the hidden-order phase.
Abstract: URu2Si2 is one of the most enigmatic strongly correlated electron systems and offers a fertile testing ground for new concepts in condensed matter science. In spite of >30 years of intense research, no consensus on the order parameter of its low-temperature hidden-order phase exists. A strong magnetic field transforms the hidden order into magnetically ordered phases, whose order parameter has also been defying experimental observation. Here, thanks to neutron diffraction under pulsed magnetic fields up to 40 T, we identify the field-induced phases of URu2Si2 as a spin-density-wave state. The transition to the spin-density wave represents a unique touchstone for understanding the hidden-order phase. An intimate relationship between this magnetic structure, the magnetic fluctuations and the Fermi surface is emphasized, calling for dedicated band-structure calculations. The strongly-correlated electron system URu2Si2 possesses a hidden-order phase whose order parameter remains unidentified. Here, the authors demonstrate the development of spin-density-wave phases in URu2Si2under high magnetic fields, providing a potential in-road to understanding this system.

Journal ArticleDOI
TL;DR: In this article, the authors report on the studies of room temperature (RT) crystal structure, electric and magnetic properties of (1-x) Pb(Fe1/2Nb 1/2)O-3 -PFWx) solid solutions through the measurements of X-ray diffraction, FTIR, scanning electron microscopy (SEM), NEF, Raman, Magnetic, Mossbauer and ferroelectric measurements.

Journal ArticleDOI
TL;DR: In this article, the noncollinear magnetic structure of a nanometer-scale stack of two metallic oxides has been demonstrated and shown to have superconductivity properties similar to ours.
Abstract: Unexpected forms of proximity-induced superconductivity can result from magnetization developing a ``twist.'' Researchers demonstrate the noncollinear magnetic structure of a nanometer-scale stack of two metallic oxides.