Stability of the low-temperature tetragonal phase in La2?xBaxCuO4 and related compounds

In La_2–x Ba _x CuO₄ (LBCO), the structural transition to a low-temperature tetragonal phase below 60 K and suppression of superconductivity are observed when the carrier density isp 1 /8 per copper. The replacement by divalent ions smaller than Ba²⁺ suppresses the static deformation of the lattice. We have found that the variationsT _d2 and superconducting transition temperatureT _c are quantitatively characterized by the averaged ionic radius at the La site or lattice parameters. This aspect of substitution could be regarded as the effect of chemical pressure, since similar variations have been reported on applying hydrostatic pressure. In La_2–x–y Nd _y (Ba, Sr) _x CuO₄,T _d2 increases with increasingy in a wide range ofp whileT _c is suppressed only at p l /8. The structural transition atT _d2 here should be ascribed mainly to the crystallochemical origin.     

EPR and vibrational studies of YVO4:Tm, Yb single crystal

A well oriented YVO₄ single crystal, with 5% Yb³⁺ and 2% Tm³⁺ nominal doping, was investigated using the Raman and EPR techniques.The EPR measurements suggest that Yb³⁺ ions occupy eight-coordinated Y³⁺ sites forming bisdisphenoids of the D_2d symmetry. An inhomogeneous distribution of rare-earth ions leads to a significant distortion of the local point symmetry (C₁). It seems that strong dipole–dipole interactions between Yb³⁺ ions are responsible for the distortion. As a result, two types of ytterbium magnetic centers appear. They correspond to paired magnetic centers and distorted isolated paramagnetic centers that are strongly sensitive to the magnetic field directions and some imperfections of the crystal. Pair centers can be recorded through the rotation around the c-crystal axis, whereas isolated centers can be measured when the crystal is rotated around the a-crystal axis. With the increasing temperature, the ytterbium signal disappeared at about 23 K and a group of narrow lines became visible. These lines, observed in the range of 240–550 mT, correspond to the Gd³⁺ (S = 7/2) ions, doped to the structure unintentionally from the basic materials.     

Reproducibility of transition temperature and critical current density of thin films of YBa2Cu3O7 on (100) LaAlO3

Submicrometer epitaxial films of YBa₂Cu₃O₇(YBCO) on (100) LaAlO₃ were made by coevaporation and furnace annealing. Samples from more than a dozen runs are used in this study. The zero resistance transition temperature (T _c) is high (89 or 90 K) if the film composition is phase pure (Ba/Y=2, Cu/Y=3) or if it is enriched in Ba and Cu. For these compositions the critical current density (J _c) at 77 K has an average value of 2×10⁵ A cm^–2, with a tendency for decreasingJ _c with increasing film thickness (0.2 to 0.8m). Variations inJ _c are not correlated with deviations from ideal stoichiometry. Steeper slopes of the resistance-temperature curves above 100 K and lower values of the room-temperature resistivity are associated with high values ofJ _c. If the film composition is enriched in Y relative to Ba and Cu,T _c decreases by several degrees.     

Optical properties of transparent Dy doped Ba2TiSi2O8 glass ceramic

The Ba₂TiSi₂O₈ is a well known piezoelectric, ferroelectric and non-linear crystal. Nanocrystals of Ba₂TiSi₂O₈ doped with 1.5 Dy³⁺ have been obtained by thermal treatment of a precursor glass and their optical properties have been studied. X-ray diffraction patterns and optical measurements have been carried out on the precursor glass and glass ceramic samples. The emission spectra corresponding to the Dy³⁺: ⁴F_9/2 → ⁶H_13/2 (575 nm), ⁴F_9/2 → ⁶H_11/2 (670 nm) and ⁴F_9/2 → ⁶H_9/2 (757 nm) transitions have been obtained under laser excitation at 473 nm. These measurements confirm the incorporation of the Dy³⁺ ions into the Ba₂TiSi₂O₈ nanocrystals which produces an enhancement of luminescence at 575 nm. At this wavelength has been demonstrated a maximum optical amplification around 1.9 cm⁻¹ (∼8.2 dB/cm).     

Morphology and conductivity studies of a new solid polymer electrolyte: (PEG)<Subscript>x</Subscript>LiClO<Subscript>4</Subscript>

A new solid polymer electrolyte, (PEG)_xLiClO₄, consisting of poly(ethylene)glycol of molecular weight 2000 and LiClO₄ was prepared and characterized using XRD, IR, SEM, DSC, NMR and impedance spectroscopy techniques. XRD and IR results show the formation of the polymer-salt complex. The samples with higher salt concentration are softer, less opaque and less smooth compared to the low salt concentration samples. DSC studies show an increase in the glass transition temperature and a decrease in the degree of crystallinity with increase in the salt concentration. Melting temperature of SPEs is lower than the pure PEG 2000. Room temperature¹H and⁷Li NMR studies were also carried out for the (PEG)_xLiClO₄ system. The¹H linewidth decreases as salt concentration increases in a similar way to the decrease in the crystalline fraction and reaches a minimum at aroundx = 46 and then increases.⁷Li linewidth was found to decrease first and then to slightly increase after reaching a minimum atx = 46 signifying the highest mobility of Li ions for this composition. Room temperature conductivity first increases with salt concentration and reaches a maximum value (σ = 7.3 × 10⁻⁷ S/cm) atx = 46 and subsequently decreases. The temperature dependence of the conductivity can be fitted to the Arrhenius and the VTF equations in different temperature ranges. The ionic conductivity reaches a high value of ∼10 ⁻⁴S/cm close to the melting temperature.     

1/f Noise properties of swift heavy ion irradiated epitaxial thin films of YBCO

Effect of 250 MeV¹⁰⁷Ag ion irradiation induced columnar defects on the noise properties of the YBCO superconductor in the normal and superconducting state have been investigated. Magnitude of the spectral density of the noise is found to scale inversely with the frequency and exhibit a quadratic dependence on the bias current confirming that the noise arises due to the resistance fluctuations. The magnitude ofS _v has been found to decrease with decrease in temperature and shows a noise peak in the transition region. The noise performance of these materials in the vicinity of the superconducting transition as well as in the normal state is found to improve by an order of magnitude after irradiation with 250 MeV¹⁰⁷Ag ions. The decrease in the magnitude of 1/f noise peak is due the irradiation induced enhanced flux pinning of the material which suppresses the flux motion induced noise in the vicinity ofT _c.     

Structural and Physical Properties of Nd Substituted Bismuth Cuprates Bi1.7 Pb0.3−x Nd x Sr2Ca3Cu4O12+y

BiPb-2234 bulk samples with nominal composition of the compound Bi_1.7Pb_0.3−x Nd _x Sr₂Ca₃Cu₄O_12+y (BSCCO) (0.025≤x≤0.10) have been prepared by the melt-quenching method. The effects of Nd substitution on the BSCCO system have been investigated by electrical resistance (R–T), scanning electron microscopy (SEM), X-ray diffraction (XRD) and magnetic hysteresis measurements. It has been the BSCCO (2212) low-T _c phase is formed for all the substitution levels, together with the BSCCO (2223) high-T _c phase. The results obtained suggest that with increasing Nd³⁺ doping for Pb²⁺ the (2223) phase existing in undoped BSCCO gradually transforms into the (2212) phase and hence all of the samples have a mixed phase formation. The R–T result of the samples show two-step resistance transition; first transition occurs at 100 K and second in an interval of 80–90 K, depending on the Nd concentration. We have found that the magnetization decreases with increasing temperature in agreement with the general characteristic of the high-T _c materials. The samples exhibit weak field dependence particularly after 2 T and changes on the magnetic hysteresis, M–H curve rather small compared to the conventional superconducting materials. The maximum critical current density, J _c, value was calculated to be 8.51×10⁵ at 4.2 K and J _c decreases with increasing temperature and the substitution level.      

Structural Studies of the Superconducting La2.5Y0.5CaBa3(Cu1?xFex)7Oz (0 ≤ x ≤ 0.1) Perovskite System by Neutron Diffraction

We have investigated the effect of Fe substitution on the structural and superconducting properties of La_2.5Y_0.5CaBa₃(Cu_1–x Fe _x )₇O _z system by Rietveld refinement of the neutron diffraction patterns of three samples with x = 0.02 (labelled B₁), x = 0.06 (B₂), and x = 0.10 (B₃) along with X-ray diffraction, resistivity, AC susceptibility, and oxygen-content measurements. Samples B₁, B₂, and B₃ are superconducting with T _c ^R=0 values of 73, 62, and 41 K, respectively. Neutron diffraction studies confirm (i) the formation of a single phase tetragonal structure (space group P4/mmm) for all three samples, (ii) Ca and Y ions substitution at the La site concomitantly displaces La onto Ba sites, and (iii) increasing x from 0.02 to 0.10 increases oxygen content (the amount of oxygen per unit cell), as well as Cu(1)— O(4) and Cu(1)— O(1) bond lengths whereas Cu(2)— O(4) bond length decreases with corresponding decrease in T _c to 41 K due to increasing occupancy of Fe ions at Cu(2) site. The change in bond lengths with oxygen content are essentially the same as those of Fe content (x). Present studies establish a correlation between the bond lengths (Cu(1)— O(1), Cu(1)— O(4), and Cu(2)— O(4)) and the measured T _c values of three samples.     

Superconductivity and Ferromagnetism of the Ru-1232 Compounds in the (Ru1?xNbx)Sr2(GdCe1.8Sr0.2)Cu2Oz System

The Ru-1232 compounds have been synthesized in the (Ru_1–xNb _x )Sr₂(GdCe_1.8Sr_0.2)Cu₂O _z system, and effects of Nb substitution for Ru on superconductivity and ferromagnetism of the Ru-1232 compounds have been investigated. First, X-ray powder diffraction study shows that nearly the single 1232 phase samples can be obtained in the x composition range from 0.0 to 0.3. Then, from the electrical resistivity study, it is found that each of the samples shows resistivity dropping phenomenon at two temperatures of T _c ^l and T _c ^h, which originates from superconductivity of the Ru-1232 phase and the Ru-1222 one, respectively. Both of the starting temperatures are lowering with increasing Nb content x. Lastly, from the magnetic susceptibility study, it is found that superconducting transition temperature T _c is 20 K for the Ru-1232 sample with x = 0.0 and the ferromagnetic transition temperature T _m is about 90 K. This study also shows that both of the values of T _c and T _m become low with increasing x from 0.0 to 0.3.     

Superconducting behavior of high-Tc YBa2Cu3O7 thin films with BaO impurity produced by pulsed laser deposition

We have investigated the superconducting behavior of high-T _c YBa₂Cu₃O₇ (YBCO) thin films containing BaO impure phase produced by pulsed laser deposition. The thin films were characterized by the standard four-probe method, X-ray diffraction (XRD), and scanning electron microscopy (SEM). XRD showed that all these thin films contained BaO impurity, with thec-axis normal to the surface of the substrates. The presence of impurity existed from substrate temperatureT _s of 727 to 796°C. When these thin films with BaO impurity were measured under the magnetic fields, it was found that the critical current densityJ _c increased slightly with increase in magnetic fieldB within the range ofB500 G, in the case ofB perpendicular to thec-axis of the film.     

GeO2 dopant induced enhancement of red emission in CaAl12O19:Mn phosphor

In order to search efficient red-emitting phosphors for white LEDs application, CaAl₁₂O₁₉:Mn⁴⁺ phosphors have been prepared by a combustion method assisted with GeO₂ flux. The influence of GeO₂ concentration and annealing temperature on the structure and luminescence intensity for the phosphors has been investigated. The mechanism for luminescence enhancement has been discussed. At GeO₂ doping concentration of 1.5 mol%, the red emission intensity increases by 81% under 330 nm UVA excitation. More isolated luminescence center Mn⁴⁺ ions rather than pairs of Mn⁴⁺-Mn²⁺ ions are formed in the lattice with the introduction of GeO₂ at high temperature oxidation, leading to the enhancement of the red emission. A feasible new way to enhance the red emission in CaAl₁₂O₁₉:Mn⁴⁺ phosphor is obtained.     

Effects of Zn doping on the structural and luminescent properties of Sr4Si3O8Cl4:Eu phosphors

Sr₄Si₃O₈Cl₄: Eu²⁺ phosphors were synthesized by the solid-reaction at high temperature. The emission intensity reaches a maximum at 0.08 mol% of Eu²⁺ concentration. The present paper mainly focused on the effects of Zn²⁺ on the crystallization behavior and photoluminescence (PL) properties of Sr₄Si₃O₈Cl₄:0.08Eu²⁺. Results suggested that no new phase is introduced by co-doping with a small amount of Zn²⁺ ions, but when co-doped with excessive amount of Zn²⁺ ions, Sr₂ZnSi₂O₇ appears. We find that the co-doping of a small amount of Zn²⁺ could remarkably improve the PL intensity of Sr₄Si₃O₈Cl₄:0.08Eu²⁺. When x = 0.05, the intensity of Sr₄Si₃O₈Cl₄:0.08Eu²⁺,xZn²⁺ was increased up to 2.3 times that of pure Sr₄Si₃O₈Cl₄:0.08Eu²⁺, which could be attributed to the flux effect of Zn²⁺ ions, and the Zn²⁺ doping reduces the opportunities of the energy transfer between Eu²⁺.     

Studies on polycrystalline Cd0.96Zn0.04Te thin films prepared by vacuum evaporation

Polycrystalline Cd_0.96Zn_0.04Te thin films are deposited onto glass substrates (Corning 7059) kept at room temperature by vacuum evaporation. The films exhibit zinc blende structure with predominant (1 1 1) orientation. The rms roughness of the films evaluated by atomic force microscope is 3.7 nm. The band gap energy of the films measured by optical transmittance measurement is 1.539 eV. The photoluminescence (PL) spectrum of the films shows intense emission due to free and bound exciton recombination and no emission associated with crystal imperfection and PL line shapes give indications of the high quality of the layers. These films have been implanted with properly mass analyzed Boron ions (¹⁰B⁺) and the effect of implantation has been analyzed by X-ray diffraction, Raman scattering and optical transmittance measurements and the results are explained on the basis of the implantation induced surface roughness and lattice disorder.     

Influence of transition metals substitution on the superconductor Bi4Ca3Sr3Cu4O y

The results of our investigation on the specimens Bi₄Ca₃Sr₃Cu_4−x T _xO _y (T=Fe, Co, Ni,x⩽0.5) synthesized in air are presented. Fe and Co substituents result in the formation of Bi₂Sr₂CuO _y -type of phase, with considerable depression ofT _c of the main phase. However, Ni is completely soluble with Cu in this concentration range without significant depression of superconducting transition temperature (T _c). This difference in the solubility behaviour of Fe and Co on the one hand and Ni on the other is explained taking into account ionic charge and coordination number mismatches.     

Effect of Proton Irradiation on the Critical Current in Tl2Ca2BaCu2O8 Bicrystal Josephson Junctions

Josephson junctions made by depositing Tl₂Ba₂CaCu₂O₈ (T1-2212) high-temperature supeconducting films on a SrTiO₃ bicrystal were irradiated at room temperature with 2-MeV protons. Changes in the critical currentI _c and the temperatureT* at whichI _c approaches zero are reported as functions of the proton fluence. Following an initial drop at low fluences. similar to a pretreatment stage.I _c becomes significantly more resistant to radiation damage. At low fluences, the sensitivity ofI _c to radiation damage is apparently dominated by the presence of grains or bridges at the junction. At high fluences the dominant effect appears to be radiation-induced decreases in the transition temperatureT _c of the banks.     

Microstructure controls and their effects on the properties of Bi2Sr2Ca1Cu2Ox superconductors

This paper reports our recent progresses in the development of Bi₂Sr₂Ca₁Cu₂O _x /Ag tape conductors for the applications of magnetic field generation in liquid helium or around 20 K, using a refrigerator. We have carried out extensive work to optimize the processing parameters, investigating the relationship between the microstructure and transportJ _c. We have found that the partial melting in oxygen atmosphere is effective to have large transportJ _c with good reproducibility. The pre-annealing and intermediate rolling (PAIR) process has been successfully applied to the multilayer conductors to improve the grain alignment and transportJ _c. TheJ _c of 5×10⁵A/cm² at 4·2 K and 10 T has been achieved, which is the highest value reported so far. Two magnets fabricated by using different types of Bi-2212/Ag conductors were tested. One is a magnet designed as an insert magnet for a 18 T-class large bore Nb-Ti/Nb₃Sn superconducting magnet. The conductor of this magnet was multifilamentary tape processed by powder-in-tube method. TheI _c was 98 A in the backup field of 18 T, which generated the self field of 1·79 T. A large pancake coil was fabricated with multilayer conductor and tested under the operation of cryocooler system. The coil was stably operated up to theJ _c of the coil at the temperatures below 30 K.     

High-pressure dc sputtering of High-Tc BPSCCO thin films withTc(0) above 100 K

High-T _c Bi(Pb)-Sr-Ca-Cu-O thin films have been made on single-crystal MgO substrates using high-pressure dc sputtering technique. X-ray studies confirm the crystallinity and highly oriented structure withc-axis perpendicular to the substrate. By optimizing the annealing schedule the formation of the high-T _c phase is stabilized. The best film exhibited superconducting transition temperature with zero-resistance temperature,T _c(0), as high as 101 K. Temperature dependence ofJ _c indicates the presence of Josephson-type weak links.     

Structure and magnetic property of CoFe2−xSmxO4 (x = 0–0.2) nanofibers prepared by sol–gel route

CoFe_2−xSm_xO₄ (x = 0–0.2) nanofibers with diameters about 100–300 nm have been prepared using the organic gel-thermal decomposition method. The composition, structure and magnetic properties of the CoFe_2−xSm_xO₄ nanofibers were investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, inductive coupling plasma mass analyzer and vibrating sample magnetometer. The CoFe_2−xSm_xO₄ (x = 0–0.2) nanofibers obtained at 500–700 °C are of a single spinel structure. But, at 800 °C with a relatively high Sm content of 0.15–0.2 the spinel CoFe_2−xSm_xO₄ ferrite is unstable and the second phase of perovskite SmFeO₃ occurs. The crystalline grain sizes of the CoFe_2−xSm_xO₄ nanofibers decrease with Sm contents, while increase with the calcination temperature. This grain reduction effect of the Sm³⁺ ions doping is largely owing to the lattice strain and stress induced by the substitution of Fe³⁺ ions with larger Sm³⁺ ions in the ferrite. The saturation magnetization and coercivity increase with the crystallite size in the range of 8.8–57.3 nm, while decrease with the Sm content from 0 to 0.2 owing to a smaller magnetic moment of Sm³⁺ ions. The perovskite SmFeO₃ in the composite nanofibers may contribute to a high coercivity due to the interface pinning, lattice distortion and stress in the ferrite grain boundary fixing and hindering the domain wall motion.     

The Influence of Bi Doping on the In Situ Growth of TlBa2Ca2Cu3O9 High-Tc Films

The in situ process—laser ablation in combination with thermal evaporation of Tl₂O—has turned out to be a preparation method for single-phase and epitaxial TlBa₂Ca₂Cu₃O₉ (1223) thin films with T _c values up to 109 K. It was found by several groups that a partial substitution of Tl by Bi simplifies the phase development of the 1223 compound in the usual two-step process. We have investigated the influence of the Bi doping on the in situ growth. X-ray measurements show that the films consisted mainly of the 1223 compound. In 300-nm thin films there was no evidence of a Bi amount in the crystal structure, but thinner films (80 nm) show a small amount of Bi. We concluded that Bi doping supports the phase development of the 1223 compound only in an early stage of the film growth. The Bi-doped films have higher T _c values up to 114 K, higher j _c values up to 6 × 10⁵ A/cm² (77 K, 0 T), and lower surface resistances of 56 m (77 K, 87 GHz) than the undoped films.     

Preparation of SrAl2O4: Eu, Dy nanometer phosphors by detonation method

SrAl₂O₄: Eu²⁺, Dy³⁺ nanometer phosphors were synthesized by detonation method. The particle morphology and optical properties of detonation soot that was heated at different temperatures (600–1100 °C) had been studied systematically by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Results indicated SrAl₂O₄: Eu²⁺, Dy³⁺ nanometer powders in monoclinic system (a = 8.442, b = 8.822, c = 5.160, β = 93.415) can be synthesized by detonation method, when detonation soot was heated at 600–800 °C. The particle size of SrAl₂O₄: Eu²⁺, Dy³⁺ is 35 ± 15 nm. Compared with the solid-state reaction and sol-gel method, synthesis temperature of the detonation method is lower about 500 and 200 °C respectively. After being excited under UN lights, detonation soot and that heated at 600–1100 °C can emit a green light.