Magnetic Behavior Research Articles

Structural and magnetic behavior of Mn-doped SnO2 nanorods for diluted magnetic semiconductors

Structural and magnetic behavior of Mn-doped SnO2 nanorods for diluted magnetic semiconductors

Magnetic Circular Dichroism of Oxide Films: Study of Electronic, Magnetic and Charge States

Semiconductor materials based on ZnO and RE3+MnO3 oxides are considered as potential candidates for spintronics. This article presents the methodology and results of studying the effect of magnetic circular dichroism for Zn1-xCoxO, Zn1-x-yCoxAlyO and RE1-x 3+Ax 2+MnO3 film structures in the visible radiation range. It has been shown that the magnetic circular dichroism behavior of the manganite films reflects not only the magnetic, but also the charge component of the material. This indicates the possibility of studying the magnetic and transport characteristics of the films using the magnetic circular dichroism spectroscopy. Since the magnetic circular dichroism effect also directly probes the ground and excited electronic states of the film, it has been obtained data that update calculated parameters for describing the manganites band structure. In the case of the Zn1-xCoxO and Zn1-x-yCoxAlyO films, the magnetic circular dichroism spectroscopy acts as a tool for detecting Co nanoparticles in the solid solution matrix of ZnO:Co and ZnO:(Co+Al).

Slow Magnetic Relaxation in a Californium Complex.

We report the synthesis and characterization of the macrocyclic californium derivative Na[Cf(H2O)(DOTA)] (DOTA = 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate), 1-Cf, which was studied in comparison to its dysprosium counterpart, Na[Dy(H2O)(DOTA)], 1-Dy. Divergent spectroscopic and magnetic behaviors were observed between 1-Cf and 1-Dy. Based upon spectroscopic measurements, we propose that accessible 5f → 6d transitions (potentially operating in tandem with charge-transfer transitions) are the major contributors to the observed broadband photoluminescence in 1-Cf. Dc magnetic susceptibility data for 1-Cf revealed lower magnetic moments than those previously observed for 1-Dy and expected for an f9 free ion, which calculations suggest is the result of greater ligand field effects. Notably, 1-Cf displays slow magnetic relaxation on the time scale of ac susceptibility measurements, making it the first example of a californium-based single-molecule magnet. A side-by-side comparison of the ac susceptibility data reveals magnetic relaxation properties that widely differ between 1-Cf and 1-Dy. This divergent relaxation behavior is attributed mainly to the inherent difference in spin-orbit coupling between Dy3+ and Cf3+.

Evolution of metallicity, enhancement of [formula omitted] and magnetic anisotropy energy in Y[formula omitted]NiIrO[formula omitted]: Hydrostatic ([111]) strain influence

Ir-based double perovskite oxides (DPO) provide a distinct electronic and magnetic behavior due to entanglement among lattice distortion, strong electron correlation, and spin–orbit coupling (SOC). In this work, we investigated the hydrostatic ([111]) strain impact on the physical properties of the Y2NiIrO6 DPO using ab-initio calculations. Unstrained motif displayed the ferrimagnetic (FiM) spin state owing to strong antiferromagnetic (AFM) interactions between Ni↑ and Ir↓ ions, further confirmed by the computed partial spin magnetic moments and 3D spin-magnetization density iso-surfaces plots. A Mott-insulating state is established with an energy band gap (Eg) of 0.43 eV due to the existence of a rare Ir+4 state having Jeff.=12 and a Curie temperature (TC) of 198 K using the Heisenberg Hamiltonian model, which is up to the experimental observations. The easy magnetic axis is the [010] (b-axis) having a giant magnetic anisotropy energy (MAE) constant of 1.7 × 108 erg/cm3. Moreover, it is predicted that strain holds the FiM spin order as a magnetic ground state for the considered range of ±8%. Notably, an electronic transition from Mott-insulating to a metallic state is established at a critical compressive strain of −8%, where the admixture of Ir 5d states appears at/around the Fermi level. On the other hand, Eg solely increases with the increase of tensile strain amplitude. Due to strong and weak hybridization, the spin/orbital magnetic moment value is reduced and enhanced as a function of compressive and tensile strains, respectively. Along with this, it is found that MAE/TC increases to 25%/18% and 15%/10% at −8% compressive and ＋8% tensile strains due to larger structural distortion than that of the unstrained one, which enhances the system potential for magnetic memory devices.

Dynamic Magnetic Susceptibility Method in Studies of Coordination Compounds

The measurement of the dynamic magnetic susceptibility is a universal method, which is used for the evaluation of magnetic properties of single molecule magnets by scientists all over the world. An information in the Russian scientific literature that can be useful for practical mastering of this method is presently insufficient. To fill this gap, in this work we present a detailed procedure of a magnetochemical experiment for observing slow magnetic relaxation in coordination compounds of 3d- and 4f-element ions and the complete characterization of the dynamics of the magnetic behavior. Special attention is given to usually omitted but important details related to all stages of studying the magnetic relaxation dynamics. The main variants of sample preparation are described, the logics of the construction of a measuring sequence and the procedure of experimental data processing are discussed, and advantages and drawbacks of some programs of the calculation of magnetic relaxation dynamics data are considered. The main concepts and equations used in experimental data analysis are presented, and the primary conclusions that can be made from the obtained results are proposed.

Design and Performance Analysis of A Linear Switched Reluctance Motor Considering End Effects

Introduction: In recent years, linear actuators have gained significant attention due to their ability to provide direct linear movement without the need for motion transformation devices. One significant challenge in the design and modeling of linear actuators is the occurrence of longitudinal end-effects. The finite length of the translator stack in linear actuators causes an unbalanced phase force, leading to discrepancies between the phases at the end and center of the actuator. Neglecting these end-effects can lead to inaccuracies in the actuator's performance and control. Methods: The objective of this study is to develop a comprehensive approach for the design, sizing, and modeling of the actuator to ensure optimal performance. An energy conversion procedure calculates the thrust force and determines the actuator's geometrical parameters. A numerical model based on the finite element method is developed to analyze the actuator's magnetic behavior and establish its characteristics. Furthermore, a thorough analysis of the end effect is conducted using two-dimensional finite element analysis. Results: To accurately capture the actuator's dynamic response and enable precise control, a mathematical model is formulated, incorporating the nonlinear behavior of inductance and incorporating the end effect factor. The proposed model demonstrates high accuracy and provides a solid foundation for the control of the linear switched reluctance actuator. Conclusion: Overall, this study contributes to the advancement of direct drive systems for industrial applications by providing a detailed design procedure and an accurate modeling approach for the linear actuator, enabling more efficient and precise control strategies.

Effects of Lu-doping on the magnetic behaviour and ordering of (Ho[formula omitted]Lu[formula omitted])2Fe2Si2C

We have investigated the effects of Lu substitution on the magnetic behaviour and ordering of (Ho1−xLux)2Fe2Si2C (x = 0.32 and 0.46) by high-resolution neutron powder diffraction, magnetisation and specific heat over the temperature range 2 to 300 K. Our study has establised that the antiferromagnetic (AFM) state is weakened upon Lu substitution and that the Néel temperature TN shifts towards lower temperature with increasing Lu content. The replacement of the magnetic Ho3+ ion by the non-magnetic Lu3+ ion of smaller atomic radius, leads to a modification of the crystal field levels, as indicated by the specific heat measurements. Neutron diffraction data analysis reveals that the magnetic structure of undoped Ho2Fe2Si2C, which exhibits a commensurate, antiferromagnetic ordering of the Ho sublattice along the b-axis with a propagation vector k = [0, 0, 12], is maintained in the Lu-doped (Ho1−xLux)2Fe2Si2C compounds.

Influence of P and C co-alloying on soft magnetic properties and crystallization behavior of FeSiBPCCu nanocrystalline alloys

In this study, multicomponent synergistic effects were adopted to enhance the glass-forming ability (GFA), processing window (PW), thermal stability, and soft magnetic properties (SMPs) of FeCuSiB nanocrystalline alloys (NAs) with high Fe and Cu contents via P and C co-alloying. The co-addition of P and C is beneficial for enhancing the GFA, expanding the PW, and increasing the crystallization resistance of the compound phases in present FeCuSiBPC alloys. Consequently, the Fe81.5Cu1.7Si3.8B9P3C1 alloy exhibited a large optimum TA window of up to 100 °C and a large tA window of 40 min for nanocrystallization. Crystallization kinetic analysis showed that the co-addition of P and C led to a high-frequency factor (v) in the precipitation of α-Fe crystals, which was related to the high nanocrystal density (Nd) of α-Fe. This result may be attributed to the nucleation of α-Fe by Cu and CuP clusters. Additionally, the co-addition of P and C increased the growth active energy (Ep) of the α-Fe crystals because of their larger atomic diffusion resistance. The high Nd and Ep values led to the formation of fine nanostructures and excellent SMPs in FeCuSiBPC alloys. Therefore, the Fe81.5Cu1.7Si3.8B9P3C1 NA obtained by annealing at 420 °C for 30 min exhibited excellent SMPs with a Bs of up to 1.78 T, a low Hc of 7.5 A/m, and a high μe of 9863 (@1kHz). This study provides technical and theoretical guidance for optimizing the composition and processability of NAs with high Fe and Cu contents, paving the way for mass production of high-performance soft magnetic NAs.

Study of Structural, Magnetic, and Thermoelectric Properties of Rare Earth-based CdCe2X4 (X = S, Se, Te) Spinels for Spintronic and Energy Harvesting Applications

Controlling the spin degree of freedom in electronics paves the way for novel approaches to employ, relocate, and store data at accelerated rates. In this regard, an in-depth examination of the structural, electronic, magnetic, and transport behaviour of CdCe2X4 (X = S, Se, Te) is undertaken. It is observed that ferromagnetic states exhibit higher energy release compared to antiferromagnetic states. Room temperature ferromagnetism is characterized by the Tc and spin-polarized density of states. The underlying mechanism in ferromagnetic behaviour is elicited in terms of crystal field energy, double exchange mechanism, exchange energies, and constants. The magnetic moment shift from Ce to other NM sites (Cd, X) is identified as a mechanism sustaining ferromagnetic character through electron exchange, thereby preventing clustering. Furthermore, the temperature-dependent thermoelectric properties are investigated, encompassing electrical and thermal conductivity, Seebeck coefficient, and power factor, recommending exploration of spinels as potential candidates for sustainable energy devices.

Effect of Al/Cr ratio on structure, magnetism, and corrosion resistance of FeCoNiCr1-xAlx high entropy alloys

This study investigates the microstructure, magnetic properties, and corrosion resistance of FeCoNiCr1-xAlx (x=0, 0.25, 0.5, 0.75, 1) high-entropy alloys using the combination of experimental methods and first-principles calculations. XRD results reveal the FCC-BCC phase transition as x increases, and FeCoNiCr1-xAlx exhibits a noticeable dual-phase structure when x=0.75. The partial segregation between Ni and Al elements is indicated by SEM-EDS observations. The magnetism of both FCC and BCC phases become strong with increasing x, and the BCC phase consistently exhibiting higher magnetism than the FCC phase. Potentiodynamic polarization curves show that Al0.25 has the highest corrosion potential and the lowest corrosion current density. Under open circuit potential conditions, due to the difference between the corrosion potential and the open circuit potential, the electrochemical impedance spectroscopy measurements indicate that the corrosion resistance of the alloys follows the order: Al0 > Al0.5 > Al0.75 > Al0.25 > Al1. Considering both the soft magnetic behavior and corrosion resistance, Al0.75 is a optimal choice. These findings provide valuable insights for developing magnetic high-entropy alloy materials with superior corrosion resistance.

Unusual Optical, Electric, and Magnetic Behaviors of OLEDs due to Exothermic/Endothermic Dexter-Energy-Transfer and Fusion Channels of Hot/Cold Triplet Excitons

Unusual Optical, Electric, and Magnetic Behaviors of OLEDs due to Exothermic/Endothermic Dexter-Energy-Transfer and Fusion Channels of Hot/Cold Triplet Excitons

Radiation-Induced Paramagnetic Centers in Meso- and Macroporous Synthetic Opals from EPR and ENDOR Data

The paramagnetic defects and radiation-induced paramagnetic centers (PCs) in silica opals can play a crucial role in determining the magnetic and electronic behavior of materials and serve as local probes of their electronic structure. Systematic investigations of paramagnetic defects are essential for advancing both theoretical and practical aspects of material science. A series of silica opal samples with different geometrical parameters were synthesized and radiation-induced PCs were investigated by means of the conventional and pulsed X- and W-band electron paramagnetic resonance, and 1H/2H Mims electron-nuclear double resonance. Two groups of PCs were distinguished based on their spectroscopic parameters, electron relaxation characteristics, temperature and time stability, localization relative to the surface of silica spheres, and their origin. The obtained data demonstrate that stable radiation-induced E’ PCs can be used as sensitive probes for the hydrogen-containing fillers of the opal pores, for the development of compact radiation monitoring equipment, and for quantum technologies.

Fe oxide modification of yerba mate waste-derived biochar and activated biochar via three methodologies: Effects of material surface properties on the Fe oxides grown and implications for paracetamol and atenolol sorption

This work presents, for the first time, the development of magnetic composites using activated biochar (BC-Act) derived from yerba mate waste. It includes an analysis of the effect of the activation process on the formation of iron oxides using the most applied methodologies, an aspect that has not been studied before. Three methodologies have been considered for Fe oxides grown: coprecipitation (COP), impregnation-pyrolysis (IP), and alkaline oxidation in the presence of nitrates (AOPN). The materials with magnetic response and good enough BET area have been used to sorb Paracetamol (PCT) and Atenolol (ATE) from aqueous solutions. The activation process has resulted in the formation of mesopores, an increase of surface area due to the destruction/release of impurities, the transformation of whewellite to calcite, and changes in magnetic behavior. These changes seem to affect the formation of Fe oxides. The COP and IP methods allow the development of magnetic composites based on BC-Act, BC-Act-COP and BC-Act-IP, with saturation magnetization of 3.1 Am2/kg and 1.5 Am2/kg, respectively, attributed to magnetite/maghemite formation and a minimal distance for manipulation by a magnetic field of 12.1 mm and 7.9 mm, respectively. These distances must be considered when developing efficient removal systems using magnetic composites. PCT was sorbed faster and more efficiently than ATE, associated with its smaller molecular size. This presents a valuable contribution to environmental sustainability and advancements in water purification, highlighting the dual advantage of converting the widely available waste product, predominantly found in South America, into an effective sorbent with magnetic characteristics, capable of removing pharmaceutical contaminants from aqueous solutions. This is done in the circular economy, avoiding the final deposition of yerba mate waste in landfills, increasing their lifespan, and safeguarding other natural and non-renewable resources, such as clays, whose preservation rather than exploitation improves environmental quality and saves energy.

Lanthanide‐Based Molecular Magnetic Semiconductors

AbstractMagnetic semiconductors, with integrated properties of ferromagnets and semiconductors, are significant for developing next‐generation spintronic devices. Herein two atomically precise clusters of dysprosium(III) tellurides, formulated respectively as [Na2(15‐crown‐5)3(py)2][(η5‐Cp*Dy)5(Te)6](py)4 (Dy5Te6, Cp*=pentamethylcyclopentadienyl; py=pyridine) and [K(2,2,2‐cryptand)]2[(η5‐Cp*Dy)6(Te3)(Te2)2(Te)3] (Dy6Te10), are reported. Crystallographic studies revealed the presence of multifarious tellurido ligands within the polyhedral cluster cores. Spectroscopic and magnetic studies showed that both clusters are single‐molecule magnets exhibiting slow magnetic relaxation behaviors at low temperatures and semiconductors with low optical band gaps comparable to benchmark semiconductors. These clusters represent probably the first lanthanide‐based molecular magnetic semiconductors.

Effect of (Zr, Ta) doping on electronic and magnetic properties of zinc-blende MgTe DMS compound: AB-initio approach

This study utilizes density functional theory (DFT) and the Korringa-Kohn-Rostoker coherent potential approximation (KKR-CPA) to explore the effects of zirconium (Zr) and tantalum (Ta) doping on the electronic and magnetic properties of zinc-blende MgTe. The electronic configurations of Mg1-x(TM)xTe (TM = Zr, Ta) were analyzed, revealing that Zr induces magnetic behavior with near-total spin polarization, while Ta doping leads to metallic behavior with partial polarization. The variations in magnetic moments are largely determined by impurity concentrations, with ferromagnetic stability in both systems driven by a double exchange interaction mechanism. Additionally, Curie temperatures exceeding room temperature were observed for specific doping concentrations. These results suggest significant potential for MgTe-based materials in spintronic applications. The findings further illustrate that Zr-doped alloys display half-metallicity, making them especially promising for future spintronics device development. KEY WORDS: DMS, KKR-CPA, Polarization, Metallic behavior, Curie temperature, Double exchange, Spintronic Bull. Chem. Soc. Ethiop. 2025, 39(1), 153-164. DOI: https://dx.doi.org/10.4314/bcse.v39i1.13

Synthesis, magnetic and structural properties of (1-x)LiFe5O8–(x)LiZn2.5Ti2.5O8 spinel solid solutions

Compounds with the spinel structure present a technologically important class of materials. Spinels show a great variety of magnetic and magnetoelectric phenomena owing to the facile entrance of transition metals in the cationic sublattices. One of such examples is lithium ferrite LiFe5O8 with high ferrimagnetic phase transition temperature and cationic order-disorder transformations. The latter are important as they influence the crystal symmetry, which is crucial for physical properties. In this work we synthesize a series of (1-x)LiFe5O8–(x)LiZn2.5Ti2.5O8 (0≤x≤1) solid solutions and characterize them with various experimental and theoretical methods. The solid solutions experience a series of concentrational phase transformations between atomically ordered (P43(1)32) and disordered (Fd3¯m) phases. The variation with concetration x of Fe3+ occupancies in cationic sublattices is studied using Mössbauer spectroscopy. The Mössbauer and magnetic measurements reveal sharp suppression of magnetic properties at x≥0.5 when the number of Fe3+ ions in the A-sublattice vanishes. The magnetic behaviour in the studied series of solid solutions is confirmed by Monte Carlo calculations with magnetic exchange interactions determined using the density functional theory.

Stress Evaluation of Ferromagnetic Materials Based on a New Barkhausen Noise Sensor Composed by High Entropy Alloy Magnetic Core

Abstract During the service of ferromagnetic structural steel materials, stress should be evaluated accurately. Although the magnetic Barkhausen noise (MBN) testing has the ability to sense stress, it can be easily interfered with by environment. In this paper, a new MBN sensor is fabricated by selecting FeCoNi(AlMn)0.25 high entropy alloy (HEA) as the case of magnetic core to improve the accuracy of stress evaluation. The process optimization results show that the stability of MBN signal characteristics is the largest when the excitation frequency is 4 Hz and the voltage is 6 V. The signal-to-noise ratio of MBN indicates that the HEA and Ni-Zn ferrite probes have better anti-interference capability. The MBN signal characteristic values peak voltage and root mean square measured by the HEA probe can linearly quantify the stress level with higher efficiency, stability, and accuracy. The underlying reason of high sensitivity of HEA probe to the variation of MBN signals is revealed based on the magnetic properties. The microstructure and the thermodynamic parameters are analyzed to clarify whether the additions of Al and Mn atoms can affect the short-ranged magnetic exchange interaction and lattice distortion, which affects the magnetization behavior of HEA. Finally, the availability of MBN sensor with HEA magnetic core to the stress evaluation on the retired slide rails of car seats is conducted, which demonstrates its great application value.

Curie-Weiss behavior and the interaction temperature of magnetic nanoparticle ensembles: Local structure strongly affects the magnetic behavior

Curie-Weiss behavior and the interaction temperature of magnetic nanoparticle ensembles: Local structure strongly affects the magnetic behavior

Nanoparticle Clustering in Supraparticles to Control Magnetic Long‐Range Interactions

AbstractTo tailor superparamagnetic iron oxide nanoparticles (SPIONs) to the specific needs of diverse application fields, it is essential to understand not only their intrinsic properties but also their interactions with each other. Theoretical models predicting/explaining the magnetization behavior of macroscopic samples containing millions of SPIONs are intricate due to the complexity of the underlying relaxation mechanisms in alternating fields. This study introduces supraparticles (SPs) as model architectures to empirically investigate magnetic interactions within and between large SPION clusters (>100 nanoparticles (NPs)). For this purpose, NP dispersions containing SPIONs and silica (SiO2)NPs as non‐magnetic building blocks are spray‐dried to form binary SPs. Selective salt‐induced agglomeration of the two building block types before spray‐drying is utilized to tailor SP architectures, including control over SPION cluster size, shape, and proximity. Magnetic particle spectroscopy (MPS), operating under ambient conditions, reveals altered magnetization behavior for different cluster structures. Not only the nearest SPION neighbors, but the whole cluster structure up to several micrometers is decisive for the magnetization behavior. This highlights the importance of long‐range magnetic interactions. This work presents a versatile approach for designing model architectures to advance empirical interaction studies between SPIONs in macroscopic samples.

Synthesis of some new transition metal complexes derived from tellurated formazanes

A novel series of organotellurium compounds based on formazane derivatives with a general formula of ArTeBr3 4 and Ar2TeBr2 5 [Ar = 2-[{4-hydroxy-3-methoxyphenyl}{4-nitrophenyldiazenyl}methylene amino]-5-nitrophenyl] were synthesized by refluxing mercurated formazane derivative ArHgCl with TeBr4 in two different mole ratios of 1:1 and 2:1, respectively, in dry dioxane solvent under an argon atmosphere. Compounds ArTeBr3 and Ar2TeBr2 were then reduced by the action of an ethanolic solution of hydrazine hydrate to obtain Ar2Te2 6 and Ar2Te 7, respectively. The ligand properties of bis(2-[{4-hydroxy-3-methoxy phenyl}{4-nitrophenyl diazenyl}methylene amino]-5-nitrophenyl) telluride (7) were examined toward several metal ions through its reaction with K2PtCl4, PdCl2 · 2 H2O, K2PtCl6, RhCl3 · 3 H2O, CoCl3 · 6 H2O and NiCl2, respectively. These compounds were characterized by FTIR, UV-Vis,1H and 13C{1H} NMR spectroscopy and mass spectrometry as well as by elemental analysis, thermal analysis, magnetic susceptibility and molar conductivity. The identification of the synthesized complexes 8-13 proved that the complexes of Pt(II), Pd(II) and Ni(II) have square pyramidal geometries and are diamagnetic, while the complexes of Pt(IV), Rh(III) and Co(III) have octahedral shapes with the same magnetic behavior. The telluride 7 behaves as a neutral pentadentate ligand.