Study of YBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>7−<Emphasis Type="Italic">δ</Emphasis></Subscript> Superconductor/Graphene Oxide Composite

The aim of this research was to fabricate YBa₂Cu₃O_7?δ (YBCO) superconductor composite with graphene oxide nanosheets and to study the effect of the graphene oxide nanosheets on YBCO superconductor properties. For this purpose, the samples of pure superconductor and superconductor composite with 0.001, 0.01, and 0.1 wt.% graphene oxide were synthesized. First, graphite oxide was made by Hummer’s chemical method; after that, graphene oxide nanosheets were produced by bath-keeper ultrasonic. Then, different amounts of graphene oxide were added to the process of superconductor fabrication, which was made by solid-state reaction method. The samples were characterized and studied by Meissner effect test, XRD analysis, FESEM imaging, EDX measurement, and ac magnetic susceptibility. The critical current density (J_c) of samples was measured by four probes method. The results showed that by increasing the weight ratio of graphene oxide, J_c and T_c decrease.     

Synthesis and Characterization of Ni<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>Cu<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>Bi<Subscript>3</Subscript> Superconductor

In this paper, we characterized the microstructure and superconducting properties of Cu-doped NiBi₃ samples. The polycrystalline Ni_1?x Cu _x Bi₃ (0 ≤ x ≤ 0.10) samples were prepared using a solid-state reaction method. The crystal structure and unit cell parameters were determined by Rietveld refinement of powder X-ray diffraction. The data showed that the main phase present corresponded to NiBi₃ without dependence on the Cu concentration, but with small quantities of Ni and Bi. The SEM and AFM measurements revealed that the main phase was inhomogeneous at microscopic level, with Bi richer regions in comparison to other regions. However, Raman spectroscopy results did not show significant changes in the spectra with Cu doping and in different regions of the samples. Another finding was that regardless of Cu doping, the superconducting transition temperature was 4.05–4.06 K.     

Enhanced Superconductivity in Double-Doping Cu<Subscript>0.15</Subscript>TaSe<Subscript>2−<Emphasis Type="Italic">x</Emphasis></Subscript><Emphasis Type="Italic">S</Emphasis><Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>

Superconducting Cu _x TaSe₂(x=0.05, 0.15) and Cu_0.15TaSe_2?x S _x (x=0, 0.5, 1, 1.5) single crystals have been systematically fabricated by a chemical vapor transport method. It is found that the double doping in TaSe₂, i.e., the simultaneous intercalation of Cu and substitution of Se by S, can substantially enhance the superconducting transition temperature. Transport property measurements give evidence of the coexistence and competition of charge density wave state and superconductivity in Cu _x TaSe₂ which provide meaningful information to understand the complex electronic states in this system. The parallel shift and the fan-shape broadening behaviors are observed in the superconducting transition curves under magnetic fields of Cu_0.15TaSeS and TaSeS, respectively, indicating an increase of coherence length and suppression of superconducting fluctuation induced by copper intercalation.     

Fabrication and Analysis of Tri-layer YBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript><Emphasis Type="Italic">O</Emphasis><Subscript>7−<Emphasis Type="Italic">δ</Emphasis></Subscript> Thick Films by Low-Fluorine MOD Method

Improving the thickness of superconducting layer in coated conductors is an effective way to enhance its critical current. In this work, tri-layer YBCO/YBCO/YDyBCO films were successfully deposited on buffered Hastelloy substrate using the multi-coating lowfluorine metal-organic decomposition (LF-MOD) method and the thickness of the films can be up to 2.4 μ m. The effects of high-temperature annealing time on microstructures and superconducting properties of the films were systematically studied. Energy dispersive X-ray spectroscopy (EDS) results reveal that there remains a large amount of F element in the upper layer of the film when the annealing time is too short. With increasing the annealing time, the fluoride-containing precursor converts to YBCO grains completely. But the coarsening of grains appeared, and the critical current density (J _c) of the film dropped slightly when the annealing time is too long. The cross-sectional scanning electron microscope (SEM) image and EDS plane analysis were applied to investigate the microstructure and element distribution of the final triple-layer YBCO films, respectively. The critical current of the final YBCO superconducting film could reach 316 A (77 k, self-field) for 1.2-cm-wide tapes with the optimal annealing conditions.     

Boron Substitution for Bi in Sr-Free Bi-2212 Superconductor of Bi<Subscript>2</Subscript>Pr<Subscript>0.5</Subscript>Ca<Subscript>2.5</Subscript>Cu<Subscript>2</Subscript>O<Subscript><Emphasis Type="Italic">z</Emphasis></Subscript>

Possibility of boron substitution for Bi and the substitution effect on superconductivity is investigated for the Bi-2212 phase of Bi-Sr-Ca-Cu-O. From X-ray diffraction study, it is found that samples in the (Bi_2−x B _x )Sr₂CaCu₂O _z system are mainly of the single 2212 phase in a composition range of 0.0≤x≤0.6, and both of the lattice parameters a and c change with increasing x up to 0.6. From measurements of the magnetic susceptibility and the electrical resistivity, the superconducting transition temperature is found to increase up to 0.6 with increasing x. These results are considered to show that boron is substitutable for Bi up to x=0.6 in the (Bi_2−x B _x )Sr₂CaCu₂O _z system and that the boron substitution causes the number of hole-carriers to decrease in this system.     

Superconducting and Magnetic Properties of Zn-doped YBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>7−<Emphasis Type="Italic">δ</Emphasis></Subscript>

The superconducting properties and AC/DC magnetic properties of YBa₂Cu_3−x Zn _x O_7−δ , (x=0.0, 0.01, 0.03, 0.05, 0.10 and 0.15) compounds were investigated. Samples were synthesized through solid-state reaction route. X-ray diffraction data confirms the single-phase orthorhombic/tetragonal crystallization for the studied samples. Thermo-Gravimetric Analysis (TGA) was done for pure and Zn-doped YBa₂Cu₃O_7−δ (YBCO) samples. Results reveal that at higher dopant levels the doped samples are more oxygen-deficient than the undoped ones. The superconducting properties of YBa₂Cu_3−x Zn _x O_7−δ system always enhance with addition of oxygen to Cu–O chains, which causes enhancement of superconducting carrier density together with orthorhombic structure. Zn substitution causes an overall reduction of superconducting condensation energy with systematic degradation of superconducting properties like T _c and J _c. This occurs via induced non-homogeneity of hole carrier density created by extended nature of perturbation on electronic structure in CuO₂ planes and its weak-link type behavior. AC susceptibility measurement reveals that Zn doping reduces the inter-granular couplings. Scanning Electron Microscope (SEM) images indicate that increment of average grain size with increasing of Zn concentration.     

Microwave dielectric properties of Ba<Subscript>4</Subscript>LaTiNb<Subscript>3−<Emphasis Type="Italic">x</Emphasis></Subscript>Ta<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>O<Subscript>15</Subscript> ceramics

High dielectric constant and low loss ceramics in the system Ba₄LaTiNb_3−x Ta _x O₁₅ (x = 0–3) have been prepared by conventional solid-state ceramic route. Ba₄LaTiNb_3−x Ta _x O₁₅ solid solutions adopted A₅B₄O₁₅ cation-deficient hexagonal perovskite structure for all compositions. The materials were characterized at microwave frequencies. They show a linear variation of dielectric properties with the value of x. Their dielectric constant varies from 53.1 to 42.3, quality factor Q_u × f from 18,790 to 28,070 GHz and temperature variation of resonant frequency from +94.3 to +33.1 ppm/°C as the value of x increases.     

Low-temperature heat capacity of Li<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>Ni<Subscript>2 − <Emphasis Type="Italic">x</Emphasis></Subscript>O<Subscript>2</Subscript> solid solutions

The heat capacity of Li _x Ni_{2 − x} O₂ (x = 0.40–0.76) oxides has been measured using an adiabatic calorimeter, and their thermodynamic functions have been determined. The results indicate that the lithium nickelate solid-solution series contains a two-phase region and that near-stoichiometric LiNiO₂ has a layered structure, in accordance with earlier results.     

Angular-Dependent Vortex Pinning Properties of YBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>7−<Emphasis Type="Italic">δ</Emphasis></Subscript>/Y<Subscript>2</Subscript>O<Subscript>3</Subscript> Quasi-Multilayers

A series of quasi-multilayers of YBa₂Cu₃O_7?δ (YBCO)/Y₂O₃ specifically 70 × (m YBCO/n Y₂O₃) were prepared on SrTiO₃ single crystal using pulsed-laser deposition (PLD) with a controlled deposition pulses of m = 40 and n = 2, 5, and 10 for YBCO and Y₂O₃, respectively. The x-ray diffraction patterns indicate that all the present quasi-multilayers exhibit good c-axis orientation. The angular dependence of critical current density (J _c ) on applied magnetic field directions are systemically measured to study the anisotropic vortex pinning performances for those quasi-multilayers. It is revealed that compared with the pure YBCO films, the quasi-multilayers with n = 2, i.e., a proper constituent pulse of Y₂O₃, exhibits the enhanced vortex pinning abilities in all angles between c-axis orientation and the applied magnetic field direction. As well, such a quasi-multilayer film (n = 2) shows the higher lift factor J _c (Θ)/ J _c (90°) and much better vortex pinning properties at high fields and high temperatures, showing promising potential for coated conductor application.     

Effect of CdTe Addition on the Electrical Properties and AC Susceptibility of YBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>7−<Emphasis Type="Italic">δ</Emphasis></Subscript> Superconductor

The effect of CdTe addition on YBa₂Cu₃O_7?δ (CdTe) _x (x = 0–0.10) has been studied. XRD patterns showed the presence of impurities including CdTe for x ≥ 0.05 wt%. The resistance versus temperature curves showed metallic behavior for all samples. The onset temperature T _{c onset} for all samples is between 90 and 92 K. The superconducting transition width, ΔT _c = 4 K for all samples except for x = 0.1 wt% where ΔT _c = 6 K. The superconducting transition determined by AC susceptibility measurement also showed little change in \(T_{\mathrm {c}\chi ^{\prime }}\) (between 89 and 92 K). However, the peak temperature T _p of the imaginary part of the susceptibility χ″, showed a drastic decrease for samples with x > 0.05 wt%. This indicated that the superconducting grains were strongly decoupled for x > 0.05 wt% due to the impurities as observed in the XRD pattern. The intergrain critical current density, J _c at T _p for the x = 0 sample is J _c (82 K) = 17 A cm^?2. These results can be useful in the fabrication of semiconductor/YBCO superconductor hybrid systems.     

Heat capacity of Li<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>Ni<Subscript>2 − <Emphasis Type="Italic">x</Emphasis></Subscript>O<Subscript>2</Subscript> solid solutions

We have synthesized Li _x Ni_{2 − x} O₂ oxides in the range x = 0.1–0.84 and showed that the solid-solution system contains a two-phase region. The heat capacity of Li _x Ni_{2 − x} O₂ has been determined by differential scanning calorimetry.     

Photoluminescent properties and Hall coefficient of Cu<Subscript>1−<Emphasis Type="Italic">y</Emphasis></Subscript>In<Subscript>1+<Emphasis Type="Italic">y</Emphasis></Subscript>Se<Subscript>2+δ</Subscript>

The photoluminescence spectra and Hall coefficient of CuInSe_2+δ and Cu_1?y In_1+y Se₂ alloys have been measured. The results, combined with structural data, have been used to identify dominant defect species and determine their energies at different deviations from stoichiometry in the alloys.     

Ordering and twinning in the nonstoichiometric phase La<Subscript>1 − <Emphasis Type="Italic">y</Emphasis></Subscript>Ca<Subscript><Emphasis Type="Italic">y</Emphasis></Subscript>F<Subscript>3 − <Emphasis Type="Italic">y</Emphasis></Subscript>

The nonstoichiometric phase La_{1 ? y} Ca _y F_{3 ? y} with a LaF₃-related structure has been studied by electron diffraction. In addition to diffraction features corresponding to twinning on the (001) and {1\(\bar 2\)0} planes, typical of LaF₃, evidence has been found for twinning on the {101} and {102} planes. This behavior is accounted for by the formation of ordering domains with an ordering direction inclined to mirror planes. It seems likely that ordering domains determine many of the properties of nonstoichiometric phases.     

Mechanism of nanostructuring in fluorite-like Ca<Subscript>1 − <Emphasis Type="Italic">x</Emphasis></Subscript>La<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>F<Subscript>2 + <Emphasis Type="Italic">x</Emphasis></Subscript>

Nanostructuring in fluorite-like Ca_{1 ? x} La _x F_{2 + x} is shown to be associated with the precipitation of an CuAu-ordered phase. The shape of the precipitates is governed by the energetics of the {001} and {111} faces of tetragonal inclusions in highly anisotropic media and is nearly cuboctahedral. The misfit strain relaxes through the generation of twins, which nucleate along the intersection lines of {001} and {111} faces. The twins impede facial development and further growth and ordering of precipitates, thereby freezing the precipitation process in its initial stage. For this reason, the phase segregation is difficult to reveal, and Ca_{1 ? x} La _x F_{2 + x} crystals appear homogeneous.     

Certification of YBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>7−<Emphasis Type="Italic">x</Emphasis></Subscript> Single Crystals

A method for evaluation of the critical temperature T _c and the width of the superconducting transition ΔT _c in HTSC single crystals has been developed. By this method, the first derivative of the temperature dependence of the resistivity, \(\frac{\partial \rho (T)}{\partial T}\), is constructed. A technique for synthesis of YBa₂Cu₃O_7?x single crystals with highly reproducible physical-mechanical properties has been described. A standard sample with T _c=94 K and ΔT _c=0.25 K has been synthesized and certified.     

Polycrystalline YBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>7−<Emphasis Type="Italic">δ</Emphasis></Subscript> with Nano-sized Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Inclusions

Series of (YBa₂Cu₃O_7−δ )_1−x (Al₂O₃) _x samples have been prepared using solid state reaction method. Various amount of nano-sized Al₂O₃ particles (∼50 nm) were added with (x=0, 0.005, 0.01, 0.02, and 0.05). The microstructure and the morphology of the polycrystalline samples have been characterized by X-ray diffraction (XRD) and atomic force microscopy (AFM). The magneto-transport properties of these samples were investigated using resistance–temperature (R–T) and current–voltage (I–V) characteristics. All samples showed an orthorhombic structure with a tendency to transformation to tetragonal phase at higher levels of nanoparticles addition. The morphology of the surface of pure samples reveals a considerable number of weak-links, randomly oriented and clean grain boundaries. While in samples with nano inclusions, grain boundaries were filled with nanosized particle and have less number of weak-links. Significant enhancement of the superconducting critical current density J _c in applied magnetic field was observed due to nano Al₂O₃ inclusions. However, further increase in the value of x decreases the transition temperature T _c and the critical current density J _c . These results were interpreted in terms of the flux pinning mechanisms in granular superconducting networks which leads to a better basic understanding of the performance of YBCO system in high applied magnetic fields.     

Fluorine doping in dilute magnetic semiconductor Sn<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>Fe<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>O<Subscript>2</Subscript>

Recent studies have reported room-temperature ferromagnetism (FM) in Fe doped SnO₂. The FM in semiconductors due to transition metal doping has been argued to be carrier mediated. Fluorine (F) doping in pure SnO₂ has been reported to significantly increase the carrier concentration. In this work, we investigated the role of F doping in the range from 0% to 0.79% on the FM of chemically synthesized single phase Sn_1?x Fe _x O₂ using X-ray diffraction, UV–Vis spectrophotometry, particle-induced X-ray emission, particle-induced gamma ray emission and magnetometry. The saturation magnetization M _s (0.03 emu/g) increased by a factor of 2.5 and the lattice volume and band gap energy decreased by 0.35 Å³ and 0.2 eV, respectively, with 0.67% F doping (F/Sn atom %) compared to the sample without any fluorine.     

Visible photoluminescence of hydrothermal synthesized Sn<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>Ni<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>O<Subscript>2</Subscript> nanostructures

Sn_1−x Ni _x O₂ nanostructures such as nanocubes, nanospheres and hollow spheres were synthesized by a simple hydrothermal method. Room temperature photoluminescence spectra of the as-synthesized samples display a strong yellow emission at about 600 nm and a weak blue emission at about 430 nm. The as-prepared and annealed Sn_1−x Ni _x O₂ (x = 0, 0.01, 0.02, 0.04) were characterized by X-ray diffraction, field emission scanning electron microscopy, Raman spectrum, UV–Vis absorption spectra, and room temperature photoluminescence spectra. By investigating the relationship between the Raman band centered at 560 cm⁻¹ and the photoluminescence of the samples, we suggest that the broad yellow emission and weak blue emission primarily originate from singly ionized oxygen vacancies and tin interstitials, respectively.     

Anisotropic ferromagnetism in Fe<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>Sn<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>O<Subscript>2</Subscript> nanostructure arrays

Periodic arrays of Fe _x Sn_1?x O₂ nanostructures were fabricated by glancing angle sputter deposition onto self-assembled close-packed arrays of 200-nm-diameter polystyrene microspheres. After annealing at 873 K for 3 h, all the films were crystallized to rutile SnO₂ and maintained good thermal stability in the morphology. Compared with Fe _x Sn_1?x O₂ flat films, arrays of Fe _x Sn_1?x O₂ nanostructures possessed larger saturation magnetic moment and exhibited both perpendicular and in-plane magnetic anisotropy, resulting from the anisotropic morphology of Fe _x Sn_1?x O₂ nanostructures. The EPR signal originating from the oxygen vacancies significantly varied with the Fe concentration and reached the strongest at x = 0.059, which is consistent with the saturation magnetization. It demonstrates that the oxygen vacancies are an important factor for the ferromagnetism of Fe _x Sn_1?x O₂ films.     

Synthesis and Characterization of LaBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>7−<Emphasis Type="Italic">δ</Emphasis></Subscript> System by Combustion Technique

This paper reports the synthesis and characterization of a lanthanum–barium–copper oxide, based on a LaBa ₂Cu ₃ O ₇ system, using a wet chemical route that enables the combustion–polymerization of citrate species, in order to generate materials with enhanced surface and textural and morphological properties for potential applications. The synthesized precursor in a form of a coordination complex was characterized by Fourier transform infrared spectroscopy (FTIR) analysis in order to evaluate the formation of homogeneous and soluble citrate species as intermediates of reaction. The morphological and structural characterizations were performed over calcined material with X-ray diffraction (XRD) and electron microscopy (scanning electron microscopy (SEM)-transmission electron microscopy (TEM)) analyses, confirming the obtention of an orthorhombic crystalline phase type Pmmm (47) in the nanometric range ≈8.9 nm. Analyses of the ceramic oxide by Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) allowed to perform qualitative and quantitative assessments of the material composition, showing that the final oxide is closely related to the desired composition, discarding the presence of carbonaceous residues of the synthesis process.