Magnetic Ordering Temperature Research Articles

The Interplay of Electronic Configuration and Anion Ordering on the Magnetic Behavior of Hydroxyfluoride Diaspores.

We report a new nickel hydroxyfluoride diaspore Ni(OH)F prepared using hydrothermal synthesis from NiCl2·6H2O and NaF. Magnetic characterization reveals that, contrary to other reported transition-metal hydroxyfluoride diaspores, Ni(OH)F displays weak ferromagnetism below the magnetic ordering temperature. To understand this difference, neutron diffraction is used to determine the long-range magnetic structure. The magnetic structure is found to be distinct from those reported for other hydroxyfluoride diaspores and shows an antiferromagnetic spin ordering in which ferromagnetic canting is allowed by symmetry. Furthermore, neutron powder diffraction on a deuterated sample, Ni(OD)F, reveals partial anion ordering that is distinctive to what has previously been reported for Co(OH)F and Fe(OH)F. Density functional theory calculations show that OH/F ordering can have a directing influence on the lowest energy magnetic ground state. Our results point toward a subtle interplay between the sign of magnetic exchange interactions, the electronic configuration, and anion disordering.

Mössbauer and magnetization measurements of multicomponent iron garnets

Four Gd-containing iron garnets were investigated using Mössbauer spectroscopy and Vibrating Sample Magnetometry over a wide temperature range, from 4K to ∼600K. The magnetic ordering temperature and hyperfine parameters determined on the basis of Mössbauer spectra for all samples were found to be surprisingly similar, differences were only noted for the average magnetic moments, which turned out to be strongly correlated with the magnetic moments of rare earth elements present in the structure. Further differences between the systems were also highlighted in measurements in the external 9T magnetic field, especially around the compensation temperature. Changes in the nature of the Mössbauer spectra were interpreted based on the crystal field approximation confirming the correctness of the interpretation of the temperature dependence of magnetization for these samples.

Investigation of structural phase stability, modified magnetic spin order and low temperature spin glass-like phase transitions in Sc-doped M-type BaFe12O19 hexaferrite

This work used two approaches of mechanical alloying before high temperature solid state reaction to synthesize BaFe12-xScxO19 (x = 0.5 to 6.0) system. Rietveld refinement of X-ray diffraction patterns showed the formation of extra phases at higher Sc doping, along with the main magnetoplumbite structure. Raman spectroscopy suggested random distribution of Sc ions at the Fe-sites of hexaferrite structure. X-ray photoelectron spectroscopy (XPS) confirmed the +3 charge state at the Fe/Sc-sites. The Fe 3s band suggested dilution of ferromagnetic 3s-3d spin exchange interactions. The neutron diffraction study re-confirmed random occupancy of the non-magnetic Sc3+ ions at Fe3+ sites of the Sc doped Ba hexaferrite system. The transformation of magnetic spin order from collinear to non-collinear state has shown spin glass-like features at low temperature regime in the dc magnetization curves. This is an effect of dilution of Fe–O–Fe ferrimagnetic super exchange interactions and spin frustration in Sc-doped samples.

High pressure neutron diffraction study of magnetic ordering in erbium

We have studied magnetic ordering in polycrystalline erbium at high pressures up to 32 GPa and low temperatures down to 10 K using neutron diffraction techniques at the Spallation Neutron Source at Oak Ridge National Laboratory, USA. For the hexagonal close-packed (hcp) phase, strong nuclear and magnetic satellite intensities permit a simultaneous refinement of the nuclear and magnetic structures. At 1 GPa of applied pressure, a modulation vector q=γc∗ with γ≈2/7 for the c-axis modulated and cycloidal phases is consistent with prior single-crystal studies at low pressures. At 6.7 GPa in the hcp phase, we find γ≈0.31, indicating a reduction in the period of the magnetic structure with respect to the crystal lattice. The magnetic ordering temperature at 6.7GPa is slightly above 60 K. At 32 GPa in the double hexagonal close-packed phase, the magnetic scattering constrains the magnetic ordering temperature to 25±5 K. Our neutron diffraction study demonstrates that the magnetic ordering persists in the high-pressure double hexagonal close-packed phase of erbiumto the highest pressure of 32 GPa.

Effects of Ni2+ doping on magnetic and magnetoelectric properties of Y-type hexaferrite BaSrCo2Fe11AlO22

Magnetoelectric hexaferrites are the promising candidate materials for low-consumption magnetic memory device application, due to the existence of room-temperature magnetoelectric effect and the tunable magnetic structure. In this work, we studied the Ni doping effect on a rare room-temperature multiferroic BaSrCo2Fe11AlO22. With the comprehensive study of magnetism, magnetoelectricity, and ferroelectric properties, magnetoelectric phase diagrams of BaSrCo2-xNixFe11AlO22 were established. Generally, Ni doping has two important effects on magnetic and magnetoelectric properties. One is to strengthen superexchange interactions, greatly enhancing magnetic order temperature. Another effect is to destabilize the noncollinear magnetic structure at high temperature, causing the absence of ME effect at room temperature. In addition, the converse ME effects have been studied, revealing that converse ME coupling strength become weakened with the increase in Ni concentration. Our systematic studies provide important clues for synthesizing high performance magnetoelectric hexaferrites.

Magnetic-ordering temperature of cobalt/nickel bimetallic nanoparticles: a Monte Carlo investigation

Magnetic-ordering temperature of cobalt/nickel bimetallic nanoparticles: a Monte Carlo investigation

Understanding and Tuning Magnetism in Layered Ising‐Type Antiferromagnet FePSe3 for Potential 2D Magnet

AbstractRecent developments in 2D magnetic materials have motivated the search for new van der Waals magnetic materials, especially Ising‐type magnets with strong magnetic anisotropy. Fe‐based MPX3 (M = transition metal, X = chalcogen) compounds such as FePS3 and FePSe3 both exhibit an Ising‐type magnetic order, but FePSe3 receives much less attention compared to FePS3. This work focuses on establishing the strategy to engineer magnetic anisotropy and exchange interactions in this less‐explored compound. Through chalcogen and metal substitutions, the magnetic anisotropy is found to be immune against S substitution for Se whereas tunable only with heavy Mn substitution for Fe. In particular, Mn substitution leads to a continuous rotation of magnetic moments from the out‐of‐plane direction toward the in‐plane. Furthermore, the magnetic ordering temperature displays non‐monotonic doping dependence for both chalcogen and metal substitutions but due to different mechanisms. These findings provide deeper insight into the Ising‐type magnetism in this important van der Waals material, shedding light on the study of other Ising‐type magnetic systems as well as discovering novel 2D magnets for potential applications in spintronics.

Exceptional magnetic and magnetoelastic behavior of rare-earth non-centrosymmetric Sm7Pd3

Magnetic compounds possessing an intrinsic combination of near-zero magnetization with high magnetic anisotropy are highly desirable for spinronic applications and memory recording. A comprehensive study of Sm7Pd3 binary compound uncovered a unique combination of strong magnetoelastic behavior, very low net magnetization, and exceptionally high magnetic coercivity. The temperature-dependent X-ray synchrotron powder diffraction study indicates the abrupt changes in the compound's lattice parameters at the magnetic ordering temperature of TC=169 K, although the crystal structure remains non-centrosymmetric hexagonal Th7Fe3-type down to 6 K. Density functional theory calculations confirm high intrinsic magnetocrystalline anisotropy of Sm7Pd3, which explains the extremely large coercivity of the polycrystalline sample, up to Hcr = 130 kOe at 2 K. This discovery brings to life a novel class of highly anisotropic materials that are distinctly different from known spintronic materials, making them interesting future systems for magnetic memory research.

Strong enhancement of magnetic ordering temperature and structural/valence transitions in EuPd3S4 under high pressure.

We present a comprehensive study of the inhomogeneous mixed-valence compound, EuPd3S4, by electrical transport, X-ray diffraction, time-domain 151Eu synchrotron Mössbauer spectroscopy, and X-ray absorption spectroscopy measurements under high pressure. Electrical transport measurements show that the antiferromagnetic ordering temperature, TN, increases rapidly from 2.8 K at ambient pressure to 23.5 K at ~19 GPa and plateaus between ~19 and ~29 GPa after which no anomaly associated with TN is detected. A pressure-induced first-order structural transition from cubic to tetragonal is observed, with a rather broad coexistence region (~20 GPa to ~30 GPa) that corresponds to the TN plateau. Mössbauer spectroscopy measurements show a clear valence transition from approximately 50:50 Eu2+:Eu3+ to fully Eu3+ at ~28 GPa, consistent with the vanishing of the magnetic order at the same pressure. X-ray absorption data show a transition to a fully trivalent state at a similar pressure. Our results show that pressure first greatly enhances TN, most likely via enhanced hybridization between the Eu 4f states and the conduction band, and then, second, causes a structural phase transition that coincides with the conversion of the europium to a fully trivalent state.

Crystal structure, magnetic and transport properties of Fe0.25TaSe2

The Fe0.25TaSe2 polycrystalline samples have been synthesized using two routes of solid-state reactions and various heat treatments and cooling conditions. The obtained samples have been studied by x-ray diffraction, magnetization and electrical resistivity measurements. It has been revealed that various methods of preparation and heat treatment do not have a strong effect on the lattice parameters of the main phase in the samples, but they significantly affect the magnetic critical temperature and magnetic hysteresis of the samples. Depending on the sample preparation procedure magnetic ordering temperature of Fe0.25TaSe2 is observed to vary in the range 33–60 K. The coercive field values from 31.7 kOe to 65.3 kOe at T = 2 K are indicative of a very high magnetocrystalline anisotropy in this material. The observed distinctions in the magnetic characteristics of the Fe0.25TaSe2 samples obtained by various methods and after different heat treatments can be ascribed to the difference in the distribution of Fe atoms over the crystal lattice.

Exchange bias effect and compensation point in the bulk ferrimagnet Fe2CrSe4

Polycrystalline samples of the Fe2CrSe4 compound have been synthesized and studied by means of x-ray diffraction and magnetization measurements. The as-synthesized Fe2CrSe4 sample shows ferrimagnetic ordering below TN ∼ 300 K with a compensation point Tcomp ∼ 140 K. This compound is found to exhibit a large coercive field (half-width of the hysteresis loop reaches 15 kOe at 2 K) and a significant exchange bias (EB) effect below 50 K (HEB up to 6.6 kOe) after cooling in an applied field and after zero-field cooling. The exchange bias in Fe2CrSe4 is suggested to result from the presence of regions (clusters) with short-range correlations in the ferrimagnetic matrix due to the inhomogeneous distribution of iron and chromium atoms over the lattice. Additional heat treatment and subsequent rapid cooling lead to an increase in magnetic ordering temperature, the disappearance of compensation for sublattice magnetizations and a decrease in the exchange bias, thus showing the possibility of controlling the exchange bias and magnetic characteristics in the system.

Controllable phase transition of two-dimensional ferromagnetic chromium telluride thin films grown by molecular beam epitaxy

Two-dimensional (2D) Cr(1+δ)Te2 materials exhibit strong magnetic ordering and high Curie temperatures, making them attractive for various applications. It is crucial to achieve controllable synthesis for their successful integration into device technologies. In this study, we present the synthesis of phase-controllable 2D Cr(1+δ)Te2 films on the Si (111) substrate via molecular beam epitaxy. The composition and phase transition of the as-grown Cr(1+δ)Te2 films are characterized by using in-situ reflection high-energy electron diffraction, scanning tunneling microscopy, ex-situ X-ray photoelectron spectroscopy, X-ray diffraction, and theoretical calculations. At low growth temperatures, by carefully adjusting the film thickness from 2 to more than 3 layers, we achieve precise control over the phase of Cr(1+δ)Te2, from CrTe2 to Cr intercalated Cr2Te3. At a relatively elevated growth temperature, it is demonstrated that the Cr(1+δ)Te2 phase is independent of the film thickness, only Cr2Te3 forms and its growth mode is thickness-dependent. These phase transitions at low growth temperatures and growth mode changes at elevated growth temperatures are attributed to interfacial effects and the phase stability of Cr(1+δ)Te2 compounds. Additionally, we utilize scanning tunneling spectroscopy and computations to gain insights into the electronic properties of Cr2Te3. The magnetic measurements reveal that the 30-nm Cr2Te3 film exhibits ferromagnetic behavior with a Curie temperature of about 180 K. Our work offers a robust method for the controllable growth of high-quality 2D Cr(1+δ)Te2 films on Si substrates, providing an ideal platform for investigating their intrinsic properties and advancing the development of 2D magnet-based spintronics devices.

Tuning strategy for Curie-temperature enhancement in the van der Waals magnet Mn1+xSb2−xTe4

The van-der-Waals antiferromagnetic topological insulator MnBi2Te4 is one of the few materials that realize the sought-after quantum anomalous Hall (QAH) state and quantized surface charge transport. To assess the relevance of its isostructural analog MnSb2Te4 as a potential QAH candidate, the roles of Mn/Sb site mixing and cationic vacancies need to be clarified. Recent findings have shown that non-stoichiometry in Mn1±xSb2∓xTe4 is an efficient tuning knob to achieve a net spin-polarized state and to raise the magnetic ordering temperature well above that of MnBi2Te4. Here, we report the crystal structure, the bulk and the surface magnetism of two new Mn1+xSb2−xTe4 samples: Mn1.08Sb1.92Te4(x ≈ 0.1) with TC = 44 K, and Mn2.01Sb1.19Te4(x ≈ 1.0) with the record TC = 58 K. We quantify the site mixing comprehensively by combining various structural probes on powders and single crystals, and then employ bulk, local (electron spin resonance), and spectroscopic (x-ray magnetic circular dichroism) probes to connect these insights to the magnetism of these materials. We demonstrate that Mn over-stoichiometry up to x = 1.0, in combination with a particular Mn/Sb intermixing pattern and the increasingly three-dimensional character of the magnetic order, push the TC upwards. The tendency towards more robust ferromagnetism mediated by stronger interlayer exchange in Mn1+xSb2−xTe4 upon increasing x is confirmed by bulk magnetometry and by a series of density-functional-theory calculations of model structures with varying intermixing.

Increasing the Magnetic Order Temperature in Co3O2BO3:In Ludwigite.

Below 42 K, the homometallic Co3O2BO3 ludwigite forms magnetic planes separated by nonmagnetic low-spin Co3+ ions. The substitution of Co3+ by other nonmagnetic ions enhances the magnetic interactions, raising the magnetic ordering temperature. However, depending on the nonmagnetic dopant ion, the remaining Co3+ ions could adopt a high-spin state, creating magnetic frustration and lowering the magnetic transition temperature. Doping Co3O2BO3 with nonmagnetic In3+ ions favors the appearance of both high-spin Co2+ and Co3+. The In3+ ions preferentially occupy sites 4 and are randomly distributed in each site. The two-dimensional magnetic character of the parent compound, Co3O2BO3, is preserved, and the magnetic transition temperature increases to 47.8 K. Measurements of magnetization, which show metamagnetic transitions at low temperatures, and specific heat are consistent with ferrimagnetic ordering in this system. Thus, using these results and those reported in the literature, the effects caused by doping of Co3O2BO3 with different nonmagnetic +3 ions are discussed in terms of the presence of high-spin Co2+ and Co3+ in the compounds.

Neutron-powder-diffraction studies of the nuclear and magnetic structure of the double-perovskite CaxSr2−xWMnO6 (x = 0.5, 1.0, and 1.5)

The nuclear and magnetic structures of CaxSr2−xWMnO6 (x = 0.5, 1.0, 1.5) have been investigated by neutron diffraction at 295, 30 or 40 K, and 4 or 5 K. The compounds crystallized in the monoclinic symmetry with a space group P21/n. The nuclear structure consists of ordered WO6 and Mn2+O6 octahedral frameworks, with lattice constant a decreasing more rapidly than b with increasing Ca content. No structural change was found around the magnetic transition temperature, although the Mn octahedron below the magnetic order temperature exhibited a slightly compressed Jahn–Teller distortion (0.1–0.3 Å) along the c axis. A standard magnetic model was used to solve the magnetic structure, with the Mn magnetic moments ferromagnetically coupled along the a axis and anti-ferromagnetically coupled along the b and c axes, resulting in a magnetic propagation vector of k = (0,1/2, 1/2) and a magnetic superlattice of 1a × 2b × 2c. In each crystallographic cell, the Mn1–Mn2 atoms are antiferromagnetically configurated, compensating the total moment to zero by symmetry. A layer-type magnetism along the (111) crystallographic plane was confirmed to couple antiferromagnetically between these planes and ferromagnetically within them. The magnetic structure refinement confirmed an average Mn moment of 4.5 μB. Also, it reveals that the collinear magnetic Mn configuration has three possible spin orientations, namely, (with their standard deviation) [μx = (3.3 ± 0.4) μB, μy = (2.5 ± 0.3) μB, μz = (−0.7 ± 0.7) μB], [μx = (3.0 ± 0.4) μB, μy = (0.5 ± 0.2) μB, μz = (−2.8 ± 0.2) μB, and [μx = (−1.8 ± 0.4) μB, μy = (2.9 ± 0.2) μB, μz = (−2.4 ± 0.3) μB. The first configuration is estimated to be the ground state, while the other magnetic configurations are an optimum local value derived from the refinements. Combined with the density functional theory calculations, these experimental results confirm a high-spin state Mn2+ (d5) electron configuration.

Synthesis and Characterization of Cr-Doped Pb2Fe2O5 Thin Films by Reactive Magnetron Sputtering

Multiferroic materials, which exhibit simultaneous ferroelectricity, ferromagnetism, and ferro-elasticity, have attracted significant attention due to their multifunctional properties. Coupling between ferroelectric and magnetic properties has led to the development of non-volatile memory devices, transducers, magnetic field sensors, and other applications. Pb2Fe2O5 (PFO) is a promising multiferroic material due to it simultaneously exhibiting ferroelectricity and ferromagnetism at room temperature. Doping with aliovalent ions, such as Cr3+, has been proposed as an effective method for enhancing the ferroelectric and magnetic properties, consequently leading to the enhancement of multiferroic properties. The investigation shows that the lead ferrite phase (220) was present in all samples, but its abundance reduced with increasing synthesis temperature due to lead desorption. Dielectric measurements revealed that PFO films with highest Cr concentration had the highest polarization (Pr) of 72.2 μC cm−2. The study also found that the magnetization of PFO films was up to 9.5·10−7 μAm2 at an ambient temperature of 5 K, and the magnetic ordering temperature was 363 K, corresponding to the magnetic ordering temperature of chromium oxides. The morphology of Cr doped PFO films changed with increasing chromium content, resulting in a reduction in grain size and an increase in the film density.

Direct observation of topological magnon polarons in a multiferroic material

Magnon polarons are novel elementary excitations possessing hybrid magnonic and phononic signatures, and are responsible for many exotic spintronic and magnonic phenomena. Despite long-term sustained experimental efforts in chasing for magnon polarons, direct spectroscopic evidence of their existence is hardly observed. Here, we report the direct observation of magnon polarons using neutron spectroscopy on a multiferroic Fe2Mo3O8 possessing strong magnon-phonon coupling. Specifically, below the magnetic ordering temperature, a gap opens at the nominal intersection of the original magnon and phonon bands, leading to two separated magnon-polaron bands. Each of the bands undergoes mixing, interconverting and reversing between its magnonic and phononic components. We attribute the formation of magnon polarons to the strong magnon-phonon coupling induced by Dzyaloshinskii-Moriya interaction. Intriguingly, we find that the band-inverted magnon polarons are topologically nontrivial. These results uncover exotic elementary excitations arising from the magnon-phonon coupling, and offer a new route to topological states by considering hybridizations between different types of fundamental excitations.

Theoretical investigation of magnetic and thermal properties in Dy1−x Sc x Ni2 series

We report on the thermal and magnetic properties of Dy1−xScxNi2 series compounds (x=0.1,0.3,0.5,and0.7), which were investigated through a model Hamiltonian including the exchange, Zeeman, and crystalline electric field interactions. We investigated the effect of Sc substitution on the Dy site on the magnetic and magnetocaloric properties of these compounds. Theoretical results were simulated for heat capacity, entropy, and the magnetocaloric effect quantities. Our model reproduced the decrease of the magnetic ordering temperature and of the isothermal entropy change peaks as Sc concentration increases. Our theoretical results were confronted with experimental data from the literature, showing good agreement.

Role of structural, morphological, and electronic characteristics in investigating the low temperature transport and magnetic behavior of Sr doped Sm2NiMnO6

Oxide double perovskites of the form R2NiMnO6 (R= rare-earth) are known to possess the multifunctional behavior. Herein, we have induced structural and electronic modifications in Sm2NiMnO6 system by Sr doping to form Sm2−xSrxNiMnO6 (x = 0.0, 0.2, and 0.4) and accordingly investigated the structural, morphological, electronic, dielectric, magnetic and magnetoresistance properties. Sm2NiMnO6 has monoclinic structure with P21/n space group and doping with Sr does not change the phase of compound. Microstructure studies suggest a decrease in the grain size with increase in Sr doping while elemental overlay and analysis suggest the presence of known elements in uniformity. Chemical valency indicates the existence of mixed valence of Ni and Mn cations along with presence of oxygen vacancies in all the sample of Sm2−xSrxNiMnO6 (x = 0.0, 0.2, and 0.4). Frequency (200 Hz to 2 MHz) and low temperature (100–320 K) dependence of dielectric measurements have been carried out to observe the behavior of dielectric constant and dielectric loss. With increase in concentration of Sr, the dielectric constant decreases while the dielectric loss increases. Temperature variation of ac conductivity as well as resistivity suggests the negative temperature coefficient of resistance, depicting the semiconducting behavior of all the samples. Temperature variation of magnetization in terms of field cooled (FC) and zero field cooled (ZFC) curves shows the presence of two magnetic transitions in all the three samples. One pertains to paramagnetic to ferromagnetic transition temperature and another is due to downturn in magnetization at lower temperature. Sr doping also causes an increase in the magnetic ordering temperature. Field variation of magnetization shows the ferromagnetic nature of all the three samples, where the saturation magnetization decreases with increase in temperature as well as increase in Sr concentration. Temperature dependence of resistivity at different magnetic fields indicates the presence of magnetoresistance effect in all the three samples. These studies highlight the role of Sr doping in determining and influencing the various physical properties discussed in this paper and the importance of these double perovskite systems for future material design and various technological applications.

High-entropy effect at rare-earth site in DyNi

We report the structural and magnetic properties of RNi (R = Dy, Tb1/3Dy1/3Ho1/3, and Gd1/5Tb1/5Dy1/5Ho1/5Er1/5) to investigate the high-entropy effect at the rare-earth site. The lattice parameters are almost unchanged by the increase of configurational entropy, which is due to the successive partial substitution of Dy by a pair of rare earth elements located on both sides of Dy in the Periodic Table. All compounds exhibit ferromagnetic ground states. The replacement of Dy with Tb + Ho, which does not have magnetic interactions in competition with Dy, does not affect the magnetic ordering temperature. Although (Gd1/5Tb1/5Dy1/5Ho1/5Er1/5)Ni shows the Curie temperature close to that of DyNi, an additional magnetic anomaly, which would be a spin reorientation, is observed probably due to the introduction of competing magnetic interactions between R = Gd and Er compounds and R = Tb, Dy, and Ho ones. We have also assessed the magnetocaloric effect, and the configurational entropy dependence of the magnetic entropy change reflects that of the temperature derivative of the magnetic susceptibility. Our analysis suggests the possibility of enhancing magnetocaloric properties by designing the anisotropy of rare-earth magnetic moments in the high-entropy state.