Decrease In Lattice Parameter Research Articles

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.

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.

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.

Microwave-Irradiation Suppresses the Jahn-Teller Distortion in Spinel LiMn2O4 Cathode Material for Lithium-Ion Batteries

Jahn-Teller (J-T) distortion remains the key challenge to realizing the full electrochemistry potential of the commercialized LiMn2O4 cathode material for lithium-ion batteries. In this work, the application of microwave irradiation to suppress the limiting J-T distortion in pristine LMO (LMO-p) materials and improve the electrochemistry of lithium-ion batteries has been reported. Unlike thermal heating, microwave irradiation inhibits J-T distortion. To establish the underlying science behind the impact of microwave irradiation, both the pristine (LMO-p) and the microwave-treated counterpart (LMO-m) are subjected to several characterization techniques, including synchrotron XRD, XPS, powder neutron diffraction (PND), MAS 7Li NMR, Raman and BET analysis. These techniques prove that LMO-m possesses the needed physico-chemical properties that explain: i) suppressed J-T distortion (such as an increased average Mn oxidation state (i.e., nMn ≥ 3.5+ or Mn4+/Mn3+ > 50%)), decreased lattice parameter, enhanced BET surface area, and enhanced structural crystallinity), and ii) improved electrochemical performance (such as increased specific discharge capacity, electronic and Li-ion transfer kinetics, and Coulombic efficiency). The findings in this work are relevant for the realization of low-cost and environmentally benign scale-up modification processes for LMO spinel and related cathode materials for the development of high performance lithium-ion batteries.

Phase decomposition of AlCrFeCoNiCu0.5 HEA thin films by vacuum annealing

The most attractive advantages of high entropy alloy (HEA) thin films are their excellent properties, such as high strength and high corrosion and oxidation resistance, with a lower material cost. However, the thermal stability of the HEA thin films is always controversial. This is critical since the thermal stability of metals and alloys is closely related to the material's performance at high temperatures and also determines the application field of the material. The question of how will the nanocrystalline high entropy alloy thin film perform in terms of thermal stability needs to be clarified urgently. In this research, the thermal stability of AlCrFeCoNiCu0.5 HEA thin film fabricated by cathodic arc deposition was investigated at 500 °C as a function of time during vacuum annealing. X-Ray Diffraction (XRD), High-Resolution Transmission Electron Microscopy (HRTEM) and Transmission Kikuchi Diffraction (TKD) were applied to analyze the chemistry and microstructure of HEA thin films in detail. The results showed that there was no obvious change in the elemental compositions of the films after annealing, but the elemental distribution of the annealed films was different from the as-deposited film, especially at the film surface and film-substrate interface for the 24 h-annealed sample. The existence of the FeCo phase with B2 structure was a significant sign to demonstrate that the spinodal decomposition occurred in the single face-centered-cubic (FCC) phase matrix of the film during annealing. Simultaneously, the segregation of Cu and Cr near the film-substrate interface and the penetration of Ni and Cu towards the Si substrate were clearly observed. These unusual phenomena indicated that the thermal stability of HEA was not always excellent. Also, it was noticed that a few Kirkendall voids forming at the film-substrate interface after 24 h of annealing would affect the adhesion of the film. Additionally, heat recovery and recrystallization were achieved by 500 °C annealing, which were confirmed by the decrease of lattice parameter and the increase of grain size in the 24 h-annealed thin film. Furthermore, the hardness and elastic modulus of the thin films before and after annealing were measured by nanoindentation. The results showed all the thin films exhibited excellent mechanical properties, and the optimal hardness and elastic modulus of 7.7 ± 0.3 GPa and 183.9 ± 4.4 GPa were obtained after 3 h-annealing.

Isotropic pressure induced structural, electronic, photocatalytic, elastic and mechanical properties of RbPbF3: GGA-PBE and HSE03 based computational estimation

The main objective of this study is to present a comprehensive computational analysis, with Generalized Gradient Approximations (GGA) and Heyd–Scuseria–Ernzerhof (HSE03) correlation functionals, of the structural, optoelectronic, photocatalytic and elastic properties of Rubidium Lead Fluoride (RbPbF3) under the systematic isotropic pressure range of 0–55 GPa. Under stress a systematic decrease in lattice parameters and band gap (4.869 eV − 1.105 eV) is observed upto 55 GPa. For comprehensive evaluation of band gap, PDOS and EPDOS have also been determined. Photocatalytic properties of RbPbF3 under stress demonstrate the best photocatalytic water-splitting potential, aligning with the band gap estimation. The significant variation in optical parameters is found with a varying stress array from 0–55 GPa. Optically this compound can be utilized as a UV detector because absorption bands are seen in the UV spectrum. The material exhibits mechanical stability, and ductile behavior, with ionic and covalent bonding. The anisotropic nature is observed in our estimated results.

Effects of Mn doping on the structural, linear and nonlinear optical properties of Gd2O3 nanoparticles

We report on the effects of Mn doping on the structural, linear, and nonlinear optical properties of Gd2-xMnxO3 nanoparticles (x = 0.00, 0.03, 0.05, and 0.10). The Gd2-xMnxO3 powders were prepared using sol-gel process. The x-ray diffraction technique shows that the Mn3+ doping results in a small decrease in lattice parameter and an increase in crystallite size. UV–visible measurements were carried out in the wavelength range of 200–800 nm. The direct optical band gap estimated using Tauc model decreases with increasing Mn content from 5.152 to 5.008 eV, while Urbach energy increases from 0.753 to 1.012 eV. Moreover, the insertion of Mn results in a significant enhancement in the optical parameters (refractive index, extinction coefficient, absorption coefficient, dielectric constants (ε', ε"), optical and electrical conductivity. The dispersion energy (Ed) increases from 24.13 to 30.1 eV, while the single oscillator energy (E0) declines lightly from 10.28 to 9.998 eV with the increase of Mn content. With Mn doping an enhancement in the static linear refractive index (n0) and high-frequency dielectric constant (ε∞) were also observed. Analysis of linear and nonlinear optical parameters shows that the presence of manganese enhanced the linear optical susceptibility (χ(1)), third-order non-linear susceptibility (χ(3)), and non-linear refractive index (n2). These optical results show the potential applications of Gd2-xMnxO3 nanoparticles (x = 0.00, 0.03, 0.05 and 0.10) in various optical devices.

Synthesis, characterizations and magnetic properties of nanoscale CoVxFe2-xO4 (0.0 ≤ x ≤ 0.9) materials synthesized via sol-gel autocombustion route

Nanostructured materials of CoVxFe2-xO4 (0.0 ≤ x ≤ 0.9) have been synthesized by sol-gel autocombustion method. Phase purity and nanocrystalline nature of the materials were examined by powder XRD measurements. Morphology and microstructure of the materials were ascertained by FESEM technique. The estimated crystallite sizes (d) decrease from 30 nm to 8 nm, as a result of progressive increase in V content, x, in CoVxFe2-xO4 materials. The values of the observed lattice parameters (a) decrease continuously as a function of increasing V content, x, i.e. from 8.349(5) Å to 8.284(5) Å for the values of x = 0.0 and x = 0.9, respectively. Alterations of M − O bond lengths in CoVxFe2-xO4 materials in FTIR studies indicate the incorporation of vanadium in cobalt ferrite. The values of the saturation magnetizations (Ms) and coercivities (Hc) of CoVxFe2-xO4 materials are found to be in the range of 77.58 emu/g – 37.76 emu/g and 1264 Oe – 991 Oe for various values of x from x = 0.0 to x = 0.9, respectively. The observed trends in magnetic parameters of CoVxFe2-xO4 materials have been interpreted on basis of increasing vanadium content in the materials, cation distributions, size and surface effects.

Enhanced dielectric and magnetic properties of magnetodielectric La2−xPrxCoMnO6 for spintronic applications

La2−xPrxCoMnO6 (x = 0.5, 1.0, 1.5 and 2.0) double perovskites were prepared via sol gel method. X-ray diffraction peak profile inveterate the nonexistence of impurity phases in the prepared system. Rietveld refinement suggested that ordered monoclinic (P21/n) phase exist along with disordered orthorhombic (Pbnm) and rhombohedral (R3c) structural phases. A decrease in unit cell volume and lattice parameters is observed with increase in Pr content which is in agreement with the difference in ionic radii of La and Pr ions. Morphological and compositional study using FESEM with EDX suggested that grain size lies in micrometer range and signifies the purity of developed samples. Dielectric constant as well as tangent loss exhibit dispersive behavior at lower frequencies and higher temperatures. The strong effect of bond angle, anti-site disorder and grain size is observed on dielectric properties. Due to large bond angle and large antisite disorder, LPCMO2 exhibited largest value of dielectric constant among all developed compositions. Cole-Cole plots proposed a non-Debye type relaxation and indicated NTCR (negative temperature coefficient of resistance) behavior for the synthesized compositions. Ac conductivity showed increasing tendency with rise in both frequency as well as temperature. Increase in dc conductivity with temperature proposed semiconducting behavior of prepared samples that can be explained on the basis of Thermal activation (TA) and Variable range hopping (VRH) models. The saturation magnetization (Ms) showed a strong correlation with bond angle, tilting of CoO6/MnO6 octahedra and grain size i.e. LPCMO2 is having largest Ms whereas lowest Ms is exhibited by LPCMO3 which may be due to variation in exchange interaction which strictly depends on bond angle and tilting of MO6 octahedra. Enhanced magnetic properties make these materials useful for spintronic devices and magnetic storage. Dielectric and magnetic properties of the prepared samples depend strongly on ˂Co-O-Mn˃ bond angle and have same variation tendency with Pr substitution which indicates coupling between these properties.

Evolution of structural-phase state and properties of hypereutectoid steel rails at long-term operation

The methods of modern physical materials science were used to analyze the evolution of microhardness, tribological properties, dislocation substructure and phase composition of the rails with increased wear resistance and contact endurance of DT 400 IR category after missed tonnage of 187 million gross tons on the experimental ring of Russian Railways. It is shown that extremely long-term operation of the rails is accompanied by a decrease (3.1 times) in wear parameter of the rolling surface and an increase (1.4 times) in microhardness, scalar dislocation density (1.5 times) and Fe3C carbide content (1.24 times). Operation of the rails led to a decrease in the crystal lattice parameter, which correlates with an increase in the content of iron carbide. We made the assumptions about physical causes of the change in parameters.

Influence of synthetic temperature on structural and magnetic properties of Dy substituted Ni nanoferrite

ABSTRACT Dy substituted Ni ferrite nanoparticles with composition NiFe1.95Dy0.05O4 were synthesized by using the citric acid sol–gel auto combustion method. The samples were sintered at temperatures of 400°C, 700°C, and 900°C. The X-ray diffraction measurements clearly showed the formation of a cubic spinel structure along with a small orthoferrite phase for all the sintered samples. The crystallite size increases from 17.79 to 39.36 nm while the grain size increases from 50.70 nm to 83.05 nm. The lattice parameter and lattice volume decrease with increasing sintering temperature was observed. The Spinel ferrite structure of prepared samples has been confirmed from FTIR spectra. With increasing sintering temperature saturation magnetization increases from 25.80 emu/gm to 49.48 emu/gm while the coercivity value decreases from 207.95 Oe to 165.43 Oe. Increasing saturation magnetization and decreasing coercivity values with increasing sintering temperature make the synthesized nanoparticles suitable for high-density data storage devices.

Electroacoustic Effect and Electrical Superconductivity of Metals

The paper discusses the conditions under which superconductivity of metals would be detected at atmospheric pressure and at room temperature. One of the possible directions of research to achieve these conditions is to change the phonon spectrum of metals in order to increase the Debye temperature, and therefore to increase the temperature of the superconducting transition Tc. According to the idea of the work and to the estimates made in it, the maximum frequency of phonons nmax in metals can be increased by the short-term action of an external constant electric field (electric pulse). The duration of the pulse should be (10–5–10–7) s. The voltage of the constant electric field source is U » 1V. A decrease in the crystal lattice parameter should be accompanied by an increase in the maximum phonon frequency nmax and, accordingly, by an increase in the Debye temperature. The characteristic size of the sample, in which the change in electron concentration can be realized, should not exceed the length of electron shielding in metals, i. e. ≈ 10–8 m. The sequential action of a certain number of electric field pulses can maintain a superconducting state in a metal sample for some finite time.

Mössbauer and X-ray Studies of Radiation-Induced Processes in Nb-Zr Alloys Implanted with 57Fe Ions.

The effect of implanting 57Fe ions on the crystal structure of Nb-Zr alloys has been studied using Mössbauer spectroscopy on 57Fe nuclei and X-ray diffraction. As a result of implantation, a metastable structure was formed in the Nb-Zr alloy. The XRD data indicated a decrease in the crystal lattice parameter of niobium; that is, there was a compression of the niobium planes when implanted with iron ions. Mössbauer spectroscopy revealed three states of iron. The singlet indicated a supersaturated Nb(Fe) solid solution; the doublets characterized the diffusion migration of atomic planes and crystallization of voids. It was shown that the values of the isomer shifts in all three states did not depend on the implantation energy, which indicates the invariance of the electron density on the 57Fe nuclei in the studied samples. The resonance lines of the Mössbauer spectra were significantly broadened, which is typical for materials with low crystallinity and a metastable structure that is stable at room temperature. The paper discusses the mechanism of radiation-induced and thermal transformations in the Nb-Zr alloy, which leads to the formation of a stable well-crystallized structure. A Fe2Nb intermetallic compound and the Nb(Fe) solid solution formed in its near-surface layer, while Nb(Zr) remained in the bulk.

Phase evolution in the UO2–CeO2 system under oxidizing and reducing conditions: X-ray diffraction and spectroscopic studies

The solid-solution formation mechanism and defect dynamics in U1-xCexO2±δ solid solutions have been investigated by means of X-ray diffraction (XRD) analysis, Raman spectroscopy, and X-ray absorption near-edge structure (XANES) spectroscopy. Diffraction studies have revealed the formation of single-phase solid solutions with a fluorite-type structure at x ≤ 0.2 and a single-phase fluorite-type structure with broadened diffraction peaks, attributed to inhomogeneity in the O/M ratio, at 0.3 ≤ x ≤ 0.8 under reducing conditions. Oxidizing conditions result in the formation of single-phase solid solutions with fluorite-type structure at x ≥ 0.4. Upon the formation of Ce3+ in solid solutions at x ≤ 0.2 under reducing conditions, charge neutrality is achieved through oxygen vacancy creation and formation of higher oxidation states of uranium through a charge compensation mechanism. Lattice parameter–composition relationships for fluorite-type phases synthesized under oxidizing conditions show a decrease in lattice parameters as compared to their stoichiometric counterparts due to the oxidation of U4+ to U5+/U6+. XANES studies provide direct experimental evidence of the presence of Ce3+ in solid solutions, despite synthesis under oxidizing conditions.

Investigation of Physiochemical Impact of Organic Molecule L-Lysine on Ammonium Dihydrogen Phosphate Single Crystal for Optoelectronics Applications

Ammonium dihydrogen phosphate (ADP) single crystals along with the incorporated 0.5 and 1% L-lysine, an organic molecule which possesses a good nonlinear response, were grown with the vision to meet the requirements of the optoelectronic industry. The inclusion of the L-lysine molecule in the crystal was confirmed by the XRD and EDX. The experiment not only confirms the inclusion level of the impurity but also the capability of the amino acid molecule to bond hydrogen within the crystal facet. A minor decrease in lattice parameters was reported for all ADP: L-lysine crystals compared with pure ADP. The structures of the grown crystals were identified as tetragonal with the space group I42d by the single-crystal XRD analysis. Vibrational signatures and functional groups were confirmed using FTIR spectroscopy. The thermal stability and decomposition temperatures of 0.5 and 1% L-lysine-added crystals were measured by TG/DTA and found to be 203 °C and 207 °C, respectively. The UV–visible transmission spectra prove a higher transparency for doped crystals as compared to pure crystals; therefore, these doped crystals can be considered the best option for the frequency doubling process in a broad range of visible and near-IR spectra. The improved hardness of the doped crystals was confirmed by the Vickers hardness data. The nonlinear optical (NLO) behaviour investigated using a second-harmonic generation (SHG) technique, indicating an efficient quadratic nonlinear coefficient of ADP: Lysine crystals at a 1064 nm initial wavelength, shows about 1.5-fold higher efficiency compared with undoped ADP.