Progress in Critical Current Density (<Emphasis Type="Italic">J</Emphasis><Subscript><Emphasis Type="Italic">c</Emphasis></Subscript>) in Sintered MgB<Subscript>2</Subscript> Bulks

The present paper focuses on methods of further improving the flux pinning and critical current density of disk-shaped MgB₂ bulk superconductors by adding excess Mg metal in combination with an optimum silver content and optimized processing conditions. Bulk MgB₂ samples were produced by in situ solid-state reaction in Ar gas ambient using high purity commercial powders of Mg metal and 1.5 wt% carbon-coated amorphous B powders mixed in a fixed ratio of Mg/B = 1.1:2. Further, 4 wt% silver was added to improve flux pinning as well as mechanical performance of the bulk MgB₂ material. The magnetization measurements confirmed a sharp superconducting transition with T_c,onset at around 37 K, which is only by 1 K lower than in bulk MgB₂ material produced without carbon-coated amorphous boron. The critical current density (J_c) values significantly improved in the MgB₂ material with 4 wt% of silver and 1.5 wt% of carbon-coated amorphous boron, sintered at 775 ^°C for 3 h. At 20 K, this sample showed J_c at around 500 and 350 kA/cm² in the self-field and 1 T, respectively, which makes it suitable for several industrial applications.     

Influence of coronene addition on some superconducting properties of bulk MgB<Subscript>2</Subscript>

This study reports the effect of coronene (C₂₄H₁₂) addition on some superconducting properties such as critical temperature (T_c), critical current density (J_c), flux pinning force density (F_p), irreversibility field (H_irr), upper critical magnetic field (H_c2), and activation energy (U₀), of bulk MgB₂ superconductor by means of magnetisation and magnetoresistivity measurements. Disk-shaped polycrystalline MgB₂ samples with varying C₂₄H₁₂ contents of 0, 2, 4, 6, 8, 10 wt%, were produced at 850 °C in Ar atmosphere. The obtained results show an increase in field-J_c values at 10 and 20 K resulting from the strengthened flux pinning, and a decrease in critical temperature (T_c) because of C substitution into MgB₂ lattice, with increasing amount of C₂₄H₁₂ powder. The H_c2(0) and H_irr(0) values are respectively found as 144, 181, 172 kOe, and 128, 161, 145 kOe for pure, 4 wt% and 10 wt% C₂₄H₁₂ added samples. The U₀ depending on the magnetic field curves were plotted using thermally activated flux flow model. The maximum U₀ values are respectively obtained as 0.20, 0.23 and 0.12 eV at 30 kOe for pure, 4 wt% and 10 wt% C₂₄H₁₂ added samples. As a result, the superconducting properties of bulk MgB₂ at high fields was improved using C₂₄H₁₂, active carbon source addition, because of the presence of uniformly dispersed C particles with nanometer order of magnitude, and acting as effective pinning centres in MgB₂ structure.     

Ac Susceptibility Measurements and Mechanical Performance of Bulk MgB<Subscript>2</Subscript>

The effects of Ar ambient pressure (vacuum and 0, 10, and 20 B) and annealing times (0.5 and 1 h) on microstructural, superconducting, and mechanical properties of bulk superconducting MgB₂ are investigated. The samples are produced using the solid-state reaction method. X-ray diffraction (XRD) and scanning electron microscopy (SEM) measurements are performed for determination of the crystal structure and surface morphology of MgB₂ samples, respectively. The superconducting properties are studied by AC magnetic susceptibility measurements. Microhardness analyses are made using the Vickers microhardness test for determination of mechanical properties of all samples. Increasing the Ar pressure decreases the lattice parameters and hence the average grain size. Increasing the annealing time results in larger lattice parameters and larger grain formation. The susceptibility measurements revealed a two-step transition which is reminiscent of granular superconductors. The intra-grain transition temperature is determined to be 38.4 K for all samples. The inter-grain transition temperature of 37.2 K is obtained for samples produced under Ar ambient pressure. The samples produced under Ar ambient pressure have better superconducting properties than the ones produced in vacuum. Increasing the annealing time under vacuum further decreases the superconducting properties probably due to Mg loss.     

Effect of Ag Addition on the Surface Topography and the Vibrational Dynamics of MgB<Subscript>2</Subscript>

We fabricated MgB₂ samples with Ag additions using in situ solid-state reaction via a single-step sintering to study the effect of Ag on the structural, vibration, and superconducting properties of MgB₂ samples. Ag addition to MgB₂ resulted in a significant improvement in J _c although no appreciable effect was observed in the lattice parameters and the superconducting transition temperature T _c. Dramatic increase in the grain size was observed with Ag addition and topographic measurements with atomic force microscopy revealed the formation of Ag–Mg nanoparticles 5–20 nm in size at 2 and 4 wt% Ag additions. The fact that these samples showed high J _c values suggests that the nanoparticles formed as a result of Ag addition are responsible for enhanced flux pinning. Raman spectroscopy measurements showed that Ag additions also increased disorder in the system and thereby affected the line width of the Raman active E _2g mode.     

Comparative Experimental and Density Functional Theory (<Emphasis Type="Italic">DFT</Emphasis>) Study of the Physical Properties of MgB<Subscript>2</Subscript> and AlB<Subscript>2</Subscript>

In the present study, we report an intercomparison of various physical and electronic properties of MgB₂ and AlB₂. In particular, the results of phase formation, resistivity ρ(T), thermoelectric power S(T), magnetization M(T), heat capacity (C _P ), and electronic band structure are reported. The original stretched hexagonal lattice with a=3.083 Å, and c=3.524 Å of MgB₂ shrinks in c-direction for AlB₂ with a=3.006 Å, and c=3.254 Å. The resistivity ρ(T), thermoelectric power S(T) and magnetization M(T) measurements exhibited superconductivity at 39 K for MgB₂. Superconductivity is not observed for AlB₂. Interestingly, the sign of S(T) is +ve for MgB₂ the same is ?ve for AlB₂. This is consistent with our band structure plots. We fitted the experimental specific heat of MgB₂ to Debye–Einstein model and estimated the value of Debye temperature (Θ _D) and Sommerfeld constant (γ) for electronic specific heat. Further, from γ, the electronic density of states (DOS) at Fermi level N(E _F) is calculated. From the ratio of experimental N(E _F) and the one being calculated from DFT, we obtained value of λ to be 1.84, thus placing MgB₂ in the strong coupling BCS category. The electronic specific heat of MgB₂ is also fitted below T _c using α-model and found that it is a two gap superconductor. The calculated values of two gaps are in good agreement with earlier reports. Our results clearly demonstrate that the superconductivity of MgB₂ is due to very large phonon contribution from its stretched lattice. The same two effects are obviously missing in AlB₂, and hence it is not superconducting. DFT calculations demonstrated that for MgB₂, the majority of states come from σ and π 2p states of boron on the other hand σ band at Fermi level for AlB₂ is absent. This leads to a weak electron phonon coupling and also to hole deficiency as π bands are known to be of electron type, and hence obviously the AlB₂ is not superconducting. The DFT calculations are consistent with the measured physical properties of the studied borides, i.e., MgB₂ and AlB₂.     

Studies on the Composite System of Bi-2212 Glass Ceramic and MgB<Subscript>2</Subscript> Superconductors

The composites of glass ceramic Bi-2212 and MgB₂ superconductors were prepared at ambient conditions. The transmission electron microscopy images of the composite samples illustrate the presence of glass ceramic inclusions in bulk MgB₂. Temperature-dependent magnetization of the composite samples shows two superconducting transitions: one at 80 K corresponding to the Bi-2212 phase and a second one at 39 K corresponding to the MgB₂ phase, suggesting that the two superconducting phases are separated with clear boundaries. The critical current density (J _c) and pinning force values are increased in composite systems by an order of magnitude compared to that of individual samples. The pinning mechanism in the composite sample is the same as in the matrix phase. Reduced field maxima (h _max) are observed at 0.15 for composite samples. A low value of h _max for composite samples indicates the random orientation of grain boundaries and repulsive pinning force in the composite samples.     

Enhancement of Critical Current Density of MgB<Subscript>2</Subscript> by Glutaric Acid Doping: a Simultaneous Improvement on the Intrinsic and Extrinsic Properties

In this study, we report an enhancement of critical current density of bulk MgB₂ superconductors by glutaric acid (C₅H₈O₄) doping. The effects of glutaric acid doping on MgB₂ lattice resulted in a record self-field J _c of the order of 10⁶ A/cm². A simultaneous improvement in the connectivity, pinning force, and H _c2 is the major factor that determined excellent J _c performance. X-ray diffraction analysis showed that samples were single-phase MgB₂ with a minor trace of impurities. A dramatic change in grain morphology and homogeneity in grain distribution was found in the SEM images of doped samples. We observed that homogeneity in grain distribution played a crucial role in the connectivity and the upper critical field (H _c2) of the doped samples. We were able to introduce a new dopant through a two-step mixing approach which is suitable to overcome the degradation of low field and self-field J _c reported for carbon-doped MgB₂ superconductor samples.     

Time-Dependent Diffusion Coefficient of Fe in MgB<Subscript>2</Subscript> Superconductors

The iron (Fe) diffusion in superconducting MgB₂ bulk samples has been studied for sintering time durations of 15 min, 30 min, 1 h, 2 h, and 4 h at 900^°C. Fe coating bulk polycrstalline superconducting MgB₂ samples for Fe coating were prepared by pelletizing and used in the diffusion experiments with initial sintering at 800^°C for 1 h. A thin layer of Fe was coated on MgB₂ pellets by evaporation in vacuum. Effects of Fe diffusion on the structural, electrical, and superconducting properties of MgB₂ have been investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), infrared spectroscopy (IR), energy-dispersive X-ray spectroscopy (EDS), and resistivity measurements. Fe diffused samples have slightly increased critical transition temperatures and have larger lattice parameter c values, in comparison with bare samples. Fe diffusion coefficients were calculated from depth profiles of c parameter and room temperature resistivity values. Depth profiles were obtained by successive removal of thin layers from Fe diffused surfaces of the samples. Our results have shown that the Fe diffusion coefficient decreases with increasing sintering time and resistivity measurements can be utilized for determination of diffusion coefficient.     

Formation of High-Field Pinning Centers in Superconducting MgB<Subscript>2</Subscript> Wires by Using High Hot Isostatic Pressure Process

This paper demonstrates the effects of hot isostatic pressure (HIP) on the structure and transport critical parameters of in situ MgB₂ wires without a barrier. Our results show that only HIP and nano-boron allow the formation of more high-field pinning centers, which lead to the increase in critical current density (J _c) at high applied magnetic fields. Nano-boron and annealing at a low pressure increase the J _c in the low magnetic field. This indicates that nano-particles create more high-field pinning centers. In addition, the results show that nano-boron improves the connection between the grains. Scanning electron microscope results show that HIP increases the reaction rate between Mg and B, density, and homogeneity of the MgB₂ material. Additionally, HIP allows to create a structure with small grains and voids and eliminates the significance of the number of voids. High isostatic pressure allows to obtain high J _c of 10 A/mm² (at 4.2 K) in 10 T and increases irreversible magnetic field (B _irr) and upper critical field (B _c2). Measurements show that these wires have high critical temperature of 37 K.     

Preparation and crystal structure characterization of CuNiGaSe<Subscript>3</Subscript> and CuNiInSe<Subscript>3</Subscript> quaternary compounds

Samples of the quaternary chalcogenide compounds, CuNiGaSe₃ and CuNiInSe₃, prepared by direct fusion and annealing method, were characterized by X-ray powder diffraction. In each case, the crystal structure was refined using the Rietveld method. Both compounds were found to crystallize in the tetragonal system, space group P \(\bar 4\)2c (N°112), with unit cell parameter values a = 5.6213(1) Å, c = 11.0282(3) Å, V = 348.48(1) ų and a = 5.7857(2) Å, c = 11.6287(5) Å, V = 389.26(3) ų for CuNiGaSe₃ and CuNiInSe₃, respectively. These compounds have a normal adamantane structures and are isostructural with CuFeInSe₃.     

The Effect of Annealing on Phase Stability and Magnetic Properties of Hexaferrite BaFe<Subscript>12</Subscript><Emphasis Type="Italic">O</Emphasis><Subscript>19</Subscript>

The hexaferrite BaFe₁₂ O ₁₉ phase was synthesized through the mechanical alloying process followed by subsequent annealing. Rietveld refinements of as-milled powder annealed at 700 ^°C confirm the formation of the BaFe₁₂ O ₁₉ phase with the presence of an important amount of the α-Fe₂ O ₃ phase. Thus, prior mechanical milling shows much lower reaction temperature and less reaction time compared to conventional methods. Further annealing up to 900 and 1100 ^°C could not enable the formation of a single BaFe₁₂ O ₁₉ phase, reaching an optimum phase composition ratio close to BaFe₁₂ O ₁₉/ α-Fe₂ O ₃ 70/30. The crystallite size was found to be in the nanoscale level but increases with increasing temperature (BaFe₁₂ O ₁₉ = 20–62 nm; α-Fe₂ O ₃ = 31–74 nm). SEM micrographs show that as the annealing temperature rises, the particles become more regular with sharp edges and hexagonal-like shapes. Magnetic measurements reveal that both M _s and M _r increase with annealing temperature to reach maximum values at 900 ^°C then remain unchanged, associated with phase composition. The coercivity H _c increases upon annealing up to 700 ^°C to a much higher value, from 1.7 kOe for as-milled powder to 4.8 kOe. Its value then decreases, attributed to grain (particle) growth (formation of larger particles) due to high annealing temperatures: 900–1100 ^°C. The obtained composites show very interesting magnetic properties and can be considered for potential applications, such as hyperthermia, heavy metal and dye removal, and hard/soft magnetic composites.     

The H-T and P-T Phase Diagram of the Superconducting Phase in Pd:Bi<Subscript>2</Subscript>Te<Subscript>3</Subscript>

We study the magnetic field vs. temperature (H – T) and pressure vs. temperature (P – T) phase diagrams of the T _c ≈ 5.5 K superconducting phase in Pd _x Bi₂Te₃ (x ≈ 1) using electrical resistivity versus temperature measurements at various applied magnetic fields (H) and magnetic susceptibility versus temperature measurements at various applied magnetic fields (H) and pressure (P). The H – T phase diagram has an initial upward curvature as observed in some unconventional superconductors. The critical field extrapolated to T = 0 K is H _c (0) ≈ 6–10 kOe. The T _c is suppressed approximately linearly with pressure at a rate d T _c /d P ≈ ?0.28 K/GPa.     

Role of Aniline Addition in Structural and Superconducting Properties of MgB<Subscript>2</Subscript> Bulk Superconductor

In this study, the structural and superconducting properties of aniline-added MgB₂ superconductors were investigated by X-ray diffraction (XRD), thermal analysis techniques, and ac susceptibility measurements. The amount of aniline was changed from 0 to 1 mol%. Phase analysis and lattice parameters were determined from XRD measurements. X-ray diffraction analysis indicates that the main phase is MgB₂ and that there is a small amount of Mg as the secondary phase in aniline-added samples. According to the determination of lattice parameters, it is seen that the addition of aniline does not give a proper distribution with the contribution amount of a and c lattice parameters. From DSC curves, two exothermic peaks and one endothermic peak were observed in all samples. Pure and aniline-added samples were found to be dependent on the magnetic field in the ac susceptibility measurements, and the superconducting transition temperature (T _c ) was found to decrease to lower temperatures due to an increase in the amount of aniline. It has been determined that changes in the in-phase (χ ^′) and out-of-phase (χ ^″) components of the ac susceptibility by increasing the aniline amount have weakened the MgB₂ phase structure and thus cause changes in the pinning mechanism. In addition, ac losses of all the samples were calculated under external fields ranging from 160 to 1280 A/m and at 25 K.     

Structural and dielectric properties of PbMg<Subscript>1/3</Subscript>Nb<Subscript>2/3</Subscript>O<Subscript>3</Subscript>-PbZrO<Subscript>3</Subscript> solid solutions synthesized at high pressures and temperatures

(1 ? x)PbMg_1/3Nb_2/3O₃ · xPbZrO₃ (1 ? x)PMN · xPZ) solid solutions have been synthesized at a pressure of 5 GPa and temperatures from 1300 to 1700 K, and their structural and dielectric properties have been studied. The composition dependences of the average unit-cell parameter and dielectric permittivity for the solid solutions indicate that the PMN-PZ system has a morphotropic phase boundary near x = 0.65. The solid solutions have a cubic structure for x < 0.65, a rhombohedral structure in the range 0.65 < x < 0.9, and an orthorhombic structure (similar to that of PbZrO₃) for x > 0.9. The temperature and frequency dependences of dielectric permittivity suggest that the (1 ? x)PMN · xPZ samples with x < 0.65 consist of two ferroelectric phases: a relaxor with antipolar dipole order and a normal ferroelectric with a diffuse phase transition. The effect of annealing temperature on the ferroelectric state of the samples with x < 0.65 is examined. In the composition range 0.65 < x < 0.9, the samples have normal ferroelectric properties, independent of annealing temperature.     

Compounds WAl<Subscript>4</Subscript>, WAl<Subscript>3</Subscript>, W<Subscript>3</Subscript>Al<Subscript>7</Subscript>, and WAl<Subscript>2</Subscript> and Al-W-N combustion products

X-ray diffraction data are presented for combustion products in the Al-W-N system. New, nonequilibrium intermetallic compounds have been identified, their diffraction patterns have been indexed, and their unit-cell parameters have been determined. The phases α-and β-WAl₄ are shown to exist in three isomorphous forms, differing in unit-cell centering. The phases α′-, α″-, and α?-WAl₄ are monoclinic, with a ₀ = 5.272 Å, b ₀ = 17.770 Å, c ₀ = 5.218 Å, β = 100.10°; point groups C12/c1, A12/n1, I12/a1, respectively. The phases β′-, β″-, and β?-WAl₄ are monoclinic, with a ₀ = 5.465 Å, b ₀ = 12.814 Å, c ₀ = 5.428 Å, β = 105.92°; point groups A112/m, B112/m, I112/m, respectively. The compounds WAl₂ and W₃Al₇, identified each in two isomorphous forms, differ in cell metrics (doubling) but possess the same point group: P222. WAl ₂ ^′ : orthorhombic, a ₀ = 5.793 Å, b ₀ = 3.740 Å, c ₀ = 6.852 Å. WAl ₂ ^″ : orthorhombic, a ₀ = 11.586 Å, b ₀ = 3.740 Å, c ₀ = 6.852 Å. W₃Al ₇ ^′ : orthorhombic, Pmm2, a ₀ = 6.225 Å, b ₀ = 4.806 Å, c ₀ = 4.437 Å. W₃Al ₇ ^″ : orthorhombic, Pmm2, a ₀ = 12.500 Å, b ₀ = 4.806 Å, c ₀ = 8.874 Å. The new phase WAl₃: triclinic, P1, a ₀ = 8.642 Å, b ₀ = 10.872 Å, c ₀ = 5.478 Å, α = 104.02°, β = 64.90°, γ = 107.15°.     

Effect of Blocking and Superconducting Layer Doping on the Superconductivity and Magnetic Properties of Polycrystalline Sr<Subscript>2</Subscript>CaCu<Subscript>2</Subscript>O<Subscript>6</Subscript>

The possible difference in the properties upon doping the Sr₂CaCu₂O₆ superconducting or blocking layers with Fe and Eu respectively was investigated in this work. The homogeneous Sr_2?yEu_yCaCu₂O_6+δ and Sr₂CaCu_2?xFe_xO_6+δ (y = 0, 0.1, 0.5, x = 0, 0.05) compounds were produced by a high-pressure synthesis route. Judging by the magnetic susceptibility measurements, all samples exhibit a superconductivity transition and the Eu/Fe concentration dependencies on the diamagnetic moment and average T_c have been constructed using the experimental data. As a result, an unusual behavior of the T_c value was observed for the samples with doped Eu: a fivefold reduction in the europium concentration in the sample does not give a noticeable effect on the transition temperature value while the diamagnetic signal becomes more stronger. Complex superconducting dome was found for Eu-doped material: 0.1 ≤ y ≤ 0.5 region T_c vs. concentration data were approximated by inverted parabola-like curve with a maximum at y = 0.3. Difference in properties of the Eu and Fe-doped samples was also found in the behavior of the hysteresis loops showed the opposite orientations.     

Critical Temperature of Smart Meta-superconducting MgB<Subscript>2</Subscript>

Enhancing the critical temperature (T _C ) is important not only to widen the practical applications but also to expand the theories of superconductivity. Inspired by the meta-material structure, we designed a smart meta-superconductor consisting of MgB₂ microparticles and Y₂O₃/Eu³⁺ nanorods. In the local electric field, Y₂O₃/Eu³⁺ nanorods generate an electroluminescence (EL) that can excite MgB₂ particles, thereby improving the T _C by strengthening the electron–phonon interaction. An MgB₂-based superconductor doped with one of four dopants of different EL intensities was prepared by an ex situ process. Results showed that the T _C of MgB₂ doped with 2 wt% Y₂O₃, which is not an EL material, is 33.1 K. However, replacing Y₂O₃ with Y₂O₃/Eu³⁺II, which displays a strong EL intensity, can improve the T _C by 2.8 to 35.9 K, which is even higher than that of pure MgB₂. The significant increment in T _C results from the EL exciting effect. Apart from EL intensity, the micromorphology and degree of dispersion of the dopants also affected the T _C . This smart meta-superconductor provides a new method to increase T _C .     

Superconductivity in Ca<Subscript>0.5</Subscript>La<Subscript>0.5</Subscript>FBiSe<Subscript>2</Subscript>

Through the measurement of resistivity, magnetic susceptibility, and Hall effect, we discovered a novel BiSe₂-based superconductor Ca_0.5La_0.5FBiSe₂ with T _c of 3.9 K. A strong diamagnetic signal below T _c in susceptibility χ(T) is observed indicating the bulk superconductivity. The negative Hall coefficient throughout the whole temperature regime implies the dominant electron-type carriers in the sample. Different to most of BiS₂-based compounds where superconductivity develops from a semiconducting-like normal state, its resistivity in the present compound exhibits a metallic behavior down to T _c . Together with the enhanced T _c , the metallic character of the normal state implies that the electronic structure of Ca_0.5La_0.5FBiSe₂ may be different to those in the other BiS₂-based compounds.     

Crystal structure of [CH<Subscript>3</Subscript>NH<Subscript>3</Subscript>][(UO<Subscript>2</Subscript>)(H<Subscript>2</Subscript>AsO<Subscript>4</Subscript>)<Subscript>3</Subscript>]

The crystal structure of a previously unknown compound [CH₃NH₃][(UO₂)(H₂AsO₄)₃] was solved by direct methods and refined to R ₁ = 0.038 for 3041 reflections with |F _hkl | >-4σ |F _hkl |. The compound crystallizes in the monoclinic system, space group P2₁/c, a = 8.980(1), b = 21.767(2), c = 7.867(1) Å, β = 115.919(5)°, V = 1383.1(3) ų, Z = 4. In the structure of the compound, pentagonal bipyramids of uranyl ions, sharing bridging atoms with tetrahedral [H₂AsO₄]^? anions, form strongly corrugated layered complexes [(UO₂)(H₂AsO₄)₃]^? arranged parallel to the (100) plane. The protonated methylamine molecules [CH₃NH₃]⁺ form unidimensional tapelike packings parallel to the c axis and linked by hydrophilic-hydro-phobic interactions. The topology of the layered uranyl arsenate complex [(UO₂)(H₂AsO₄)₃]^? is unusual for uranyl compounds and was not observed previously. A specific feature of this topology is the presence of monodentate arsenate “branches” arranged within the layer.     

Electrical and thermodynamic properties of Cs<Subscript>0.97</Subscript> Rb<Subscript>0.03</Subscript>H<Subscript>2</Subscript>PO<Subscript>4</Subscript>

The transport properties of Cs_0.97Rb_0.03H₂PO₄ have been studied using polycrystalline samples and single crystals. The mixed salt is isostructural with cesium dihydrogen phosphate and has slightly smaller unitcell parameters. The cation substitution increases the low-temperature ionic conductivity of the material by about two orders of magnitude but has an insignificant effect on the conductivity of the high-temperature phase. The low-temperature conductivity of single-crystal samples exhibits significant anisotropy, with σ _a < σ _b±c . The conductivity of the polycrystalline material is close to σ _b±c . The substitution reduces the temperature of the superionic phase transition by 20°C and enhances the thermal stability of the high-temperature phase at low humidity (1 mol % H₂O).