Decrease In Lattice Parameter Research Articles

HIGH-FREQUENCY RESPONSE OF COMPLEX INITIAL PERMEABILITY OF Cr SUBSTITUTED Co0.5Cu0.5Fe2-xCrxO4

The Lattice parameter, density, initial permeability, saturation magnetization, and Néel temperature of the Cr substituted various Co0.5Cu0.5Fe2-xCrxO4 have been invented. It also explores how the sintering temperature affects these samples' density, porosity, grain size, and initial permeability. As the Cr content increases, the lattice parameter, density, and saturation magnetization decrease. The variation of lattice parameters, density, and maximum magnetic saturation level can be explained in the light of ionic size, atomic mass, and magnetic moment of Cr ion, respectively. However, grain size, complex initial permeability, and coercivity rise until x=0.2 and fall as the Cr concentration increases. Grain size, initial permeability, and coercivity correlated to each other. The textured structure of this ferrite was found at 1373K, confirmed by XRD and microstructural analysis. Bangladesh Journal of Physics, Vol. 29, Issue 1, pp. 25 – 38, June 2022

A comparative hybrid-DFT study of energy-efficient halide perovskite under hydrostatic pressure

Abstract To accomplish the primary aim of this research, follow these steps to conduct a thorough computational evaluation by using the Heyd–Scuseria–Ernzerhof (HSE-03) hybrid functional. This analysis will cover the structural, electrical, elastic, mechanical, anisotropic and optical properties of halide perovskite materials CsPbX3 (X = Cl, Br, and I) by applying pressure from 0 to 25 GPa. Under stress, all materials exhibit consistent decrease in lattice parameters and decrease in band-gap up to 25 GPa. To explore the electronic band structure (BS), we have estimated the TDOS (Total Density of States) and EPDOS (Elemental Partial Density of States). To further assess the material's relevance, we calculated several optical properties including absorption I (ω), extinction coefficient k (ω), refractive index n (ω), loss function L (ω), reflectivity R (ω), real part of the dielectric function ε_1 (ω) and the imaginary part ε_2 (ω). The static values of reflectivity R (ω), real part of the dielectric function ε_1 (ω) increases by applying pressure in all materials. With the pressure application, the peak of absorption peak under study perovskites shifts markedly towards higher photon energies. Moreover, its high refractive index, reflectivity and absorption, make it an important element for optoelectronic devices. The structure retains its cubic form and there is no change in phase in all three materials. The materials are stiff, unyielding, and mechanically stable demonstrating elevated resistance to shear stress based on different mechanical and elastic parameters, including Young’s modulus , bulk modulus and shear modulus. The Pugh/Frantsevich ratios, Kleinman’s parameter, Cauchy pressure and Poisson’s ratio, indicate the ductility of materials, metallic bonding characteristics, and resilience under high pressure. Additionally, distinctive anisotropy factors are used to confirm the material's anisotropic properties.

Exploring the Impact of Elevated Pressure on the Structural Dynamics of TlInS2 Crystal (I): A First-Principles Investigation with XRD, Raman, and Hirshfeld Topology

The structural dynamics of Thallium Indium Disulfide (TlInS2) crystal under elevated pressures were comprehensively investigated using a combination of X-ray diffraction (XRD), Raman spectroscopy via first-principles calculations, and Hirshfeld surface (HS) analysis. This study aims to elucidate pressure-induced modifications in the crystal structure and their associated properties of TlInS2 crystal. The findings reveal significant structural transformations as pressure increases, with XRD patterns indicating lattice compression and a critical transition from semiconductor to conductor at pressure P=6.25GPa [42]. The calculations predict a reduction in bond lengths, specifically S1-In1 and S1-Tl2, alongside a corresponding decrease in lattice parameters and unit cell volume. Raman spectroscopy corroborates these changes through shifts in phonon modes. The HS analysis provides further insights into pressure-dependent alterations in intermolecular interactions, revealing changes in voids and surface characteristics. The data gained from TlInS2's structural behavior under pressure, contributing to the optimization of its functional properties for pressure-tunable applications in high-performance electronic and optoelectronic devices.

Enhancing SrBi₂Nb₂O₉ ceramics: The role of neodymium substitution in structural, dielectric, and ferroelectric properties

This study investigates the impact of neodymium substitution for bismuth in SrBi2Nb2O9 (SBN) ceramics, a potential lead-free alternative for ferroelectric applications. X-ray diffraction analysis reveals a decrease in lattice parameters and volume with increasing Nd content. Scanning electron microscopy examines the influence of neodymium on grain morphology, showing a transition from characteristic SBN plate-like grains to a mix of plates and micro-spheres. Dielectric properties are evaluated, showing an increase in room-temperature permittivity for Nd-doped samples compared to the undoped counterparts. Additionally, the influence of Nd doping on relaxor ferroelectric behavior is studied. The Curie temperature (Tc) increases with Nd concentration, while the temperature dependence of relaxation time weakens. Ferroelectric properties exhibit significant changes due to Nd doping. Inverse permittivity versus temperature (ϵr−1 vs. T) measurements suggest an unconventional response, potentially due to lattice strain induced by the larger ionic radius of Nd. The potential influence of doping concentration on the order of the ferroelectric transition is also explored. Overall, neodymium substitution in SBN ceramics enhances their ferroelectric properties, making them promising for advanced electronic applications.

Effect of TaB2 on the powder synthesis and densification of ZrB2 ceramics by boro/carbothermal reduction of ZrSiO4

Previous research has shown that low-cost ZrSiO4 instead of ZrO2 resulted in coarse ZrB2 powders with generating SiC as secondary phase. In order to synthesize fine ZrB2 powders without SiC phase, 0 - 10 mol.% TaB2 were adopted to synthesize ZrB2 powders by boro/carbothermal reduction of ZrSiO4. A single solid solution of (Zr1-xTax)B2 was formed, characterized by decreasing lattice parameters with increasing Ta doping, while maintaining the P6/mmm space group. With the addition of 10 mol .%TaB2, the particle size of ZrB2 decreased from 2.98 μm to 0.67 μm. After spark plasma sintering at 2000°C, the relative density of (Zr0.9Ta0.1)B2 ceramics increased from 89.4±0.1% to 98.7±0.1%, the grain size decreased from 16.1±5.2 μm to 4.0±1.5 μm, and the hardness increased from 12.7 GPa to 16.6 GPa.

Iron telluride Fe1.1Te doped with TiS2 and NbS2: Appearance of superconducting state coexisting with antiferromagnetism

The effect of titanium or niobium disulfides doping of iron telluride has been studied for the first time by means of x-ray diffraction analysis, electrical resistivity and magnetization measurements. It has been revealed that an increase in the dopant content in the Fe1.1Te(TS2)y (T = Ti, Nb) systems (y = 0, 0.04, 0.08, 0.1, 0.2) is accompanied by the additional phase separation and leads to a decrease in the crystal lattice parameters of the tetragonal phase, partial suppression of antiferromagnetic ordering and an appearance of superconductivity. In doped samples a transition to the superconducting state has been detected upon cooling below Tconset ∼9 K coexisting with antiferromagnetism. Superconductivity is suggested to exhibit a granular character due to inhomogeneity of the samples and the small volume fraction of superconducting phase. The difference in the superconducting transitions for both dopant types may be associated with different morphologies and compositions of resulting phases.

Structural and electrical properties of Ni-doped MnZn ferrite synthesized via solid state reaction

Abstract MnZn ferrite is commonly studied due to its exceptional magnetic, electric, and catalytic properties, making it a promising material for hyperthermia applications, magnetic fluid, memory storage devices, drug delivery, virus detection, and photocatalysis. It was identified that divalent nickel cation substitution increases the ferrite conductivity and dielectric constant. This study targets to synthesize Ni-doped MnZn ferrite by a simpler, more convenient, and economic solid state reaction, and to investigate its influence on the structural and electrical properties of MnZn ferrite. Mn0.5-xNixZn0.5Fe2O4 (x=0.1 and 0.2) was synthesized via solid state reaction with calcination and sintering temperature at 1000 °C and 1200 °C, respectively. The structural and electrical properties of the resulting pellet were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), and electrochemical impedance spectroscopy (EIS). The XRD profile, indexed as cubic spinel, indicated good crystallinity and no impurity peaks were detected. As Ni2+ dopant concentration increases, a decrease in lattice parameter and an increase in theoretical and apparent densities were observed. This is attributed to the smaller ionic radius and greater mass of Ni2+ relative to Mn2+. Varying Ni2+ concentration significantly modified the morphology of the ferrite. At higher Ni2+, less uniformity in shape and size was evident in the SEM micrograph since Ni promotes aggregation at the surface. An increase in dielectric constant was also observed with increasing Ni2+ molar concentration. Since Ni2+ presents a high tendency to occupy B sites, its substitution promotes Fe2+ migration to A sites, augmenting Fe2+/Fe3+ hopping resulting in an increase in polarization and dielectric constant.

Indirect to direct band gap transition of ABI3 (A = Rb, Cs; B = Ca, Sr) perovskites under hydrostatic pressure for photovoltaic and optoelectronic applications: A DFT study

The objective of this study is to enhance the utilization of ABI3 (A = Rb, Cs; B = Ca, Sr) metal-halide perovskites in multiple forms of technological applications by investigating their structural, electronic, optical, and mechanical characteristics using the ab initio method. At ambient pressure, the geometry-optimized lattice constants for RbCaI3, RbSrI3, CsCaI3, and CsSrI3 are 6.19 Å, 6.45 Å, 6.22 Å, and 6.47 Å, respectively, consistent with prior research. Additionally, a significant decrease in lattice parameters and bond length is observed, which leads to increased levels of atomic interactions. Pressure narrows the band gap from the ultraviolet-to-visible region. This phenomenon promotes the transfer of electrons from the valence-to-conduction band, hence improving the performance of optoelectronic devices. Furthermore, a shift from an indirect to a direct band gap is induced by the application of pressure, which improves the material's suitability for photovoltaic applications. The covalent and ionic nature of Ca/Sr-I and Rb/Cs-I under pressure and without pressure conditions was determined using the charge density maps. Enhanced pressure significantly boosts optical absorption and conductivity in the visible spectrum, implying substantial potential for improving the efficacy of perovskite solar cells and photonic devices. Additionally, applied pressure significantly influences the mechanical properties of the entitled perovskites, leading to higher ductility and anisotropy. As a whole, this study offers insights into the scientific applications of non-toxic perovskites in different pressure environments.

Investigation of kesterite to stannite phase transition and band gap engineering in Cu2Zn1-xCoxSnS4 thin films prepared by sol-gel spin coating

In this study, the Cu2Zn1-xCoxSnS4 (CZn1-xCoxTS) films with partial cation substitution of cobalt are synthetized by sol gel spin coating, followed by sulfurization treatment. The incorporation of cobalt cation in the CZTS crystalline lattice as well as the phase transition from kesterite to stannite were confirmed by the X-ray diffraction (XRD) and Raman spectroscopy data. The XRD pattern shows peak-shifting toward higher 2θ by increasing the Co concentration, indicating a decrease in lattice parameters. The red shift of Raman peaks by increasing x from 0 to 0.6, confirms the phase transition. The CZn1-xCoxTS morphology was observed by scanning electron microscopy, showing large grain size as x increases and a good distribution of elements for all films. X-ray photoelectron spectroscopy was employed to study the valence of cations/anions and to probe the chemical bonds. The optical band gap showed a parabolic behavior versus the molar ratio Co/(Co + Zn), this deviation from Vegard’s law being induced by the difference in electronegativity between cobalt and zinc. The pure CZTS has a band gap of 1.47 eV, while for CZn0.6Co0.4TS the gap is 1.17 eV, which indicates that the incorporation of cobalt cation produces a red-shift of the band to band transition energy.

Investigations on the crystallographic stacking disordering and properties of novel Ga-containing in-plane chemically ordered (Cr2/3R1/3)2GaC (R=Y, Tb - Lu) i-MAX phases

Eight novel transition metal carbides, nanolaminated (Cr2/3R1/3)2GaC (R=Y, Tb, Dy, Ho, Er, Tm, Yb and Lu) with R in-plane chemical ordered occupation, have been synthesized with mainly Cmcm orthorhombic structure and monotonously decreased lattice parameters due to lanthanide contraction. Stacking disorderings and high-density slidings within c plane have been observed. Two characteristic in-plane sliding, along [100] or [1¯30]o directions have been analyzed with former one leading into the structural evolution between Cmcm and C2/c symmetry. Such an atomic scale co-existence of Cmcm and C2/c structures is explained by more negative charge for Ga and anisotropic bonding with Ga compared with A=Al case. Thus, the Vickers hardness, fracture strength and increased wear depth are reduced in representative (Cr2/3Lu1/3)2GaC i-MAX bulk compared with the (Cr2/3Lu1/3)2AlC counterpart.

Effects of La-Co Co-Substitution and Magnetic Field Pressing on the Structural and Magnetic Properties of SrM Hexaferrites

We carefully investigated the effects of La-Co co-substitution and magnetic field pressing (MFP) on the structural and magnetic properties of SrM hexaferrites. Samples composed of Sr1−xLaxFe12−xCoxO19 were sintered at 1230 °C for 2 h in air with sintering additives composed of 0.7 wt% CaCO3 and 0.7 wt% SiO2. A single M-type phase was confirmed to exist up to x = 0.3. Rietveld refinement revealed a slight decrease in lattice parameter a and the unit cell volume (Vcell) with an increasing x, while parameter c showed a significant decrease. The saturation magnetization (Ms) values increased from 70.90 to 72.40 emu/g with an increasing x from 0.0 to 0.15 and then decreased to 71.38 emu/g with further increasing of x to 0.3, while the anisotropy field (Ha) increased from 17.7 to 25.9 kOe, leading to a continuous increase in the intrinsic coercivity (Hci), from 3.52 to 5.00 kOe, respectively. Using the MFP process, the c-axis of M-type hexaferrite grains could be effectively aligned to the applied field direction, which significantly affected the microstructures and, thus, magnetic properties of samples. Unlike non-MFP samples, exhibiting a significant increase in the average grain size (davg) but almost unaltered average thickness (tavg) with an increasing x from 0.0 to 0.3, MFP-processed samples exhibited almost unaltered davg values but a continuous decrease in tavg. Consequently, the variation in remanent flux density (Br) versus x followed that of Ms versus x and thus exhibited the highest Br of 4.05 kG for x = 0.15, leading to the highest maximum energy product {(BH)max} of 3.62 MGOe. With an increasing x from 0.0 to 0.3, the Hci values continuously increased from 3.14 to 3.84 kOe mainly due to a continuous increase in Ha, although they were significantly lowered in comparison with those of non-MFP samples because of a large increase in Br for a given composition x. A higher Mr/Ms ratio always resulted in a larger (BH)max in our samples regardless of x. A careful comparison of the microstructures and magnetic properties between MFP and non-MFP samples provided valuable insights into a broad area of permanent magnet optimization.

Emergence of Perovskite and Hashemite-type phases in chromium doped (Ba0.90Sr0.10)(Fe1-xCrx)O3±δ oxides: Formation, Rietveld refinement and Raman spectra

Perovskite- and Hashemite-type oxides are relevant due to their applications as oxidizing agent, photocatalyst, nutrient, fuel cells, gas sensors, batteries materials. An attempt has been made here to synthesize (Ba0.90Sr0.10)(Fe1-xCrx)O3±δ(x = 0 – 1.0) and characterized with regards to structure and Raman vibrations. It depicts (a) pure cubic (Ba0.90Sr0.10)FeO3-δ phase, (b) cubic+orthorhombic, and (c) single orthorhombic (Ba0.90Sr0.10)CrO4 phase for x = 0–0.10, 0.20 – 0.80, and 1.0, respectively. It exhibits (i) decrease of cubic lattice parameter (ac)as 4.020 – 3.926 Å, (ii) expansion of orthorhombic unit cell, (iii) complete appearance of chromium in 6+ state for x = 1.0, and (iv) decrease of bond length and angle both with chromium. The bond lengths corresponding to Ba/Sr-O ∼ 2.84 Å, Fe-O ∼2.04 Å and Ba/Sr-O1 ∼ 3.227 Å, Ba/Sr-O2 ∼ 2.893 Å, Ba/Sr-O3 ∼2.859 Å have been derived for cubic (x = 0) as well as orthorhombic structure (x = 1.0), respectively. The bond angles e.g., Cr-O1-Cr ∼ 129°, Cr-O2-Cr ∼ 104.3° and Cr-O3-Cr ∼ 83.3° have been found for x = 1.0. Moreover, the bond Cr-O1 is compressed and Cr-O2 is more stretched than Cr-O3 bond. The morphology has also been changed to bigger size (nm) and shows different nature with chromium content. Raman spectra for Hashemite-type (Ba0.90Sr0.10)CrO4 reveal bands at ∼350, 360, 401, 425, 861, 886 and 904 cm−1 and arise due to symmetric (υ1, υ2) and antisymmetric (υ3, υ4) bending/ stretching mode. The present findings suggest potential applications of (Ba0.90Sr0.10)(Fe1-xCrx)O3±δ oxides.

Experimental and DFT studies of structural and optoelectronic properties of CdS, Zn doped CdS, and (Zn-Ni) co-doping CdS nanomaterials

Abstract This paper presents experimental and theoretical studies of binary semiconductor CdS, Zn:CdS, and (Zn-Ni) co-doped CdS. Thin films of pure CdS, Cd35ZnS36, and Cd34ZnNiS36 alloys grown by sol-gel spin coating were analyzed using X-ray diffraction, EDX, and UV-vis spectroscopy. The experimental results show the success of growing nanomaterials in hexagonal structures with crystallite sizes ranging from 1.6 to 2.11 nm and possessing band gaps in the region 2.30 -2.49 eV. Additionally, we investigate the structural and optoelectronic properties of these materials in the ground state using the density functional theory implemented in the WIEN2k software. The first principles calculations confirmed that the structural and optical properties of CdS align with the experimental results. For nanostructure Cd35ZnS36, the lattice parameters decrease, and the band gap increases to 2.85 eV with Zn doping. The (Zn-Ni) co-doped CdS structure optimization shows that the ferromagnetic configuration is more stable than the non-magnetic structure. The spin-polarized band structure investigations reveal that the majority spin-up channel is about 2.79 eV while the minority spin-down channel is around 2.19 eV. These results increase the importance of Zn:CdS and CdZnNiS alloys for optoelectronic and spintronic applications. The calculated optical properties of CdS, Zn:CdS, and (Zn-Ni) co-doped CdS show slight changes in refractive index and extinction coefficient with the doping and a quantitative agreement with the experimental findings.

Effects of Co on the microstructure evolution and mechanical properties of Ti-4Al-6Cr-5Mo-8 Nb alloy by ultrasonic vacuum melting

An investigation was conducted into the impact of low cobalt content on the microstructure and mechanical properties of titanium alloys. Ti-4Al-6Cr-5Mo-8 Nb-xCo (x = 0, 2, 3, 4, and 5) alloys were prepared by ultrasonic-assisted melting and casting. The changes in microstructure, mechanical properties, and the strengthening and toughening mechanisms were researched. Results show that, when the cobalt content increases from 0 to 5 wt%, the as-cast structure is all β phase. The lattice parameter of the β phase decreases from 0.3663 to 0.3114 nm, a 15% decrease. The size of primary β grains decreases from 676.8 to 310.7 μm, a 54% decrease. When the cobalt content exceeds 3 wt%, the segregation energy of cobalt increases and grain boundary segregation occurs. Grain refinement is due to constitutional supercooling caused by the β-stable element cobalt, as well as the solute drag caused by the differences in intragranular and grain boundary compositions. In addition, the size mismatch between cobalt and titanium atoms leads to lattice distortion. As the cobalt content increases from 0 to 3 wt%, the tensile strength increases from 918.1 to 1147.8 MPa, a 25% increase, while the fracture toughness increases from 51.7 to 59.7 MPa·m1/2, a 15% increase. At 5 wt% cobalt, the tensile strength and fracture toughness diminished to 247.5 MPa and 14.8 MPa·m1/2, respectively. The decrease in lattice parameters mainly lead to an increase in strength. The secondary crack leads to an increase in toughness. The decline in strength and toughness results from cobalt segregating at grain boundaries, leading to embrittlement.

Pressure-induced DFT evaluation of MSnI3 (M = K, Rb) perovskites for electronic phase transition and enhanced optoelectronic utilization

In optoelectronic device applications, perovskite materials have overtaken other compounds because of their exceptional power conversion efficiencies. Lead-based perovskites have found extensive use; however, their widespread adoption is hindered by the inherent toxicity associated with lead content. In contrast, lead-free metal halide perovskites have taken the dominant position in the commercialization of optoelectronic devices by offering high efficiency, affordability, flexibility, tunability, and environmental benefits. To better understand the structural, electronic, bonding, optical, elastic, and mechanical properties of the non-toxic MSnI3 (M = K, Rb) metal halides under different hydrostatic pressures, a first-principles simulation has been carried out with the use of density functional theory (DFT). Lattice parameters and electronic band structures have been computed using both the Generalized Gradient Approximation (GGA) and the non-local hybrid sX (Hartree-Fock screened exchange) functional. Utilizing the sX method results in enhanced band gap values for MSnI3 (M = K, Rb) perovskite compounds. The application of pressure has led to a decrease in both lattice parameters and band gaps, marking a transition from a semiconductor to a metallic state. The projection of the density of states and their electronic orbital contributions are also explored to evaluate the band structure tuning of MSnI3 (M = K, Rb) under pressure. The bond length calculation and the charge density mapping confirm the existence of both the ionic and covalent bonds in MSnI3 (M = K, Rb). Additionally, the pressure-induced calculation suggests that the bonds between both compounds will be stronger at high pressure. Increasing hydrostatic pressure causes a dramatic movement of the absorption edge of MSnI3 (M = K, Rb) perovskites into the low energy region (a red shift), which is revealed by the analysis of optical functions. The optical functions’ investigation indicates that the hydrostatic pressure allows the compounds even better for a number of possible uses. The mechanical qualities are a direct reflection of the ductile and anisotropic nature of the compounds, both of which are significantly influenced by the external pressure.

Study on the pathway of performance improvement and mechanism of Gd2O2S:Tb3+ green phosphor

To improve the luminescence performance of Gd2O2S:Tb3+, Gd2O2S:Tb3+, Tm3+, Gd2O2S:Tb3+, Dy3+, Tm3+ and Gd2O2S:Tb3+, Dy3+, Tm3+@SiO2 phosphors have been prepared by molten salt method. The samples are characterized using XRD, SEM, TEM, FT-IR, UV-Vis absorption spectroscopy, photoluminescence, cathodoluminescence and thermal stabilization tests. XRD tests and refinement results show that the crystal structure of the phosphor is still the hexagonal Gd2O2S crystalline phase and the lattice parameter decrease due to Dy3+/Tm3+ occupying the Gd3+ sites. SEM images and mapping of each element show that the particle grain and all expected elements distribute uniformly. TEM results illustrate that SiO2 coating is in an amorphous form on the surface of the powder grains. FT-IR tests indicate that SiO2 is present on the powder surface through Si-O-Gd bonding. The results of photoluminescence and cathodoluminescence show that the luminescence intensity increase 50% while adding Tm3+ into Gd2O2S:Tb3+, Gd2O2S:Tb3+, Dy3+ phosphors caused mainly by the energy transfer from Dy3+/Tm3+ to Tb3+. The core-shell structure of Gd2O2S:Tb3+, Dy3+, Tm3+@SiO2 has better photoluminescence and cathodoluminescence and the fluorescence lifetime remains unchanged while SiO2 coats phosphor. And it has good thermal stability. Its luminescence intensity at 425 K reaches 71.4% of that at room temperature, which is better than the corresponding value (46.4%) for the uncoated sample.

Quantum critical behavior of the hyperkagome magnet Mn3CoSi

β-Mn-type family alloys Mn3TX (T=Co, Rh, and Ir; X=Si and Ge) have a three-dimensional antiferromagnetic (AF) corner-shared triangular network, i.e., the hyperkagome lattice. The antiferromagnet Mn3RhSi shows magnetic short-range order over a wide temperature range of approximately 500 K above the Néel temperature TN of 190 K. In this family of compounds, as the lattice parameter decreases, the long-range magnetic ordering temperature decreases. Mn3CoSi has the smallest lattice parameter and the lowest TN in the family. The quantum critical point (QCP) from AF to the quantum paramagnetic state is expected near a cubic lattice parameter of 6.15 Å. Although the Néel temperature of Mn3CoSi is only 140 K, the emergence of the quantum critical behavior in Mn3CoSi is discussed. We study how the magnetic short-range order appears in Mn3CoSi by using neutron scattering, μSR, and bulk characterization such as specific heat capacity. According to the results, the neutron scattering intensity of the magnetic short-range order in Mn3CoSi does not change much at low temperatures from that of Mn3RhSi, although the μSR short-range order temperature of Mn3CoSi is largely suppressed to 240 K from that of Mn3RhSi. Correspondingly, the volume fraction of the magnetic short-range order regions, as shown by the initial asymmetry drop ratio of μSR above TN, also becomes small. Instead, the electronic-specific heat coefficient γ of Mn3CoSi is the largest in this Mn3TSi system, possibly due to the low-energy spin fluctuation near the quantum critical point. Published by the American Physical Society 2024

Gallium induced effect on magnetic, magnetostrictive and electrical properties of sintered NiFe2O4

This study investigates how the incorporation of Ga ions into the tetrahedral coordination sites affects the magnetic, magnetostrictive, and electrical properties of sintered NiFe2O4. All characterization was performed on the sintered NiFe2-xGaxO4 samples, which were synthesized using the autocombustion method. The sintered samples exhibit a single phase, wherein the lattice parameter decreases, and the particle size increases with the augmentation of Ga-content within the Ni-ferrite lattice. Saturation magnetization (MS) was found to be higher for x = 0.25 compared to the parent sample (x = 0), while for x = 0.5, MS was slightly lower than that of the parent sample. Both coercivity (HC) and Curie temperature (TC) exhibited a decrease with increasing 'x,' which can be attributed to the weakening of superexchange interactions (A-O-B) due to the presence of non-magnetic Ga ions. Furthermore, the maximum magnetostriction (λmax) also decreased with increasing 'x,' reflecting a magnetic dilution effect within the system. Electric modulus analysis of the dielectric response and the Jonscher power law fits AC conductivity propounded the long-range hoping for charge transportation. Also, the Cole-Cole fit of impedance spectra showed a combined effect of electrode-grain boundary, grain interior, and grain-grain boundary.

Исследование превращений переохлажденного аустенита при ступенчатой закалке стали 20Cr2Mn2SiNiMo

Currently, step quenching of steels in the temperature range of martensitic transformation, including quenching – partitioning, has found wide application in the automotive industry. Step quenching technology is successfully used to increase a set of properties, which most often include temporary tensile strength and relative elongation. The authors carried out a dilatometric study of the supercooled austenite transformations occurring in the 20Cr2Mn2SiNiMo steel, when implementing various options of step quenching with holding in the martensitic region. It was found that after single-stage quenching, single-stage quenching followed by tempering, and two-stage quenching, primary martensite, isothermal bainite, and secondary martensite are formed in various quantitative ratios. Using X-ray diffraction phase analysis, the amount of residual austenite was determined during step quenching. It has been shown that two-stage quenching makes it possible to stabilise up to 14 % of residual austenite, in the structure of the studied steel, at room temperature. Research has revealed that 20Cr2Mn2SiNiMo steel is characterised by a decrease in the crystal lattice parameter of the residual austenite, with an increase in its content in the steel structure. Uniaxial tensile and impact bending tests were carried out, and the values of the mechanical properties were determined. It has been found that during two-stage quenching, higher strength and elongation values, with lower values of relative contraction and impact strength are achieved compared to oil quenching and low-temperature tempering. The study showed that, with regard to the structural reliability of machine-building parts, step quenching is not the optimal heat treatment mode for the steel under study. The best combination of strength, ductility and impact hardness is achieved after quenching and low-temperature tempering.

Structural characterization, optical, and magnetic properties of MgTbxFe2−xO4 nano ferrite particles using a combustion technique

The citrate gel auto-combustion method was utilised to synthesis terbium-doped nanoparticles (NP) with considerable concentrations of magnesium ferrites, using the chemical formula MgTbxFe2−xO4 and an X range of 0.000 to 0.0030 (with an X step of 0.0005). At 300 K, X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transition electron microscopy (TEM), and magnetic characteristics were all determined. The XRD and TEM images indicate nanoscale ranges as well as the cubic spinel structure, which is merely phased, and confirm the normal crystallite size. The lattice parameter and volume decrease as density increases with doping of terbium. The images from the FESEM. It is evident that the grain clusters were found within the material. In the specimen's case, the highly interacting grains were found. The fourier-transformed infrared spectroscopy (FTIR) data clearly suggests that two metallic bands have formed, confirming the cubic spinel ferrites. There are two primary absorption bands visible between 200 and 650 cm−1. The UV–vis investigation demonstrates that the calculated direct band gap energy values have a violet shift. The band gab energy was reported in the range of 415.30 eV to 375.12 eV.The magnetic properties of the hysteresis loops indicate a transition from hard magnetic moments to soft magnetic moments. All magnetic properties were reduced when the Tb3+ ion was substituted. They are excellent for switching memory storage devices as well as telecommunications.