The Influence of Lithium Halides on the Superconducting Properties of YB2Cu3O7?x

The effects of addition to YBa₂Cu₃O_7–x of lithium halides (YBa₂Cu₃O_7–x (LiF) _y , and YBa₂Cu₃O_7–x (LiCl) _y ) on the structural, electric, magnetic, and transport properties are analyzed. Both structural and superconducting properties depend weakly on the lithium content up to y= 0.10. The critical temperature keeps on a value well above 91 K for a small amount of lithium halide (reaching 93.48K. for y= 0.02 in YBa₂Cu₃O_7–x (LiF) _y and 91.30 K in YBa₂Cu₃O_7–x (LiCl) _y ), but for higher concentration of Li it rapidly decreases (81.68K for y= 0.20). The same behavior is exhibited in the lower intragranular critical field. The intragranular critical current density depends on the magnetic field as a power law:j _cB ^–, with a lithium-concentration-dependent . The voltage–current characteristics follow a law typical for granular superconductors, V(I–I _c(B,T)) ^n(B,T). The dependence of the intergranular critical current, I _c, and of the exponent, n, on temperature, magnetic field, and concentration is analyzed.     

Superconductivity at 103 K in CdBa2(Ca0.7Y0.3)Cu2Oy

A cadmium analogue of the mercury system with nominal composition CdBa₂(Ca_1–xY_x)Cu₂O_y has been synthesized. Thex=0 samples contain about 12 vol.% of the 1212 phase but are not superconducting. Thex=0.3 samples are superconducting atT _on = 103 K. The EDX analysis of 18 microcrystals shows a broad cationic distribution of the different components. The observed broad superconducting transition is attributed to the variousT _c of the different microcrystals.     

Influence of hole filling by Ti on the superconductivity of YBa2Cu3O7?δ

The structural and superconducting properties of YBa₂(CU_1–x Ti _x )₃O_z samples are investigated using X-ray diffraction, ac susceptibility, and oxygen content measurements. The effect of increasing Ti concentration in YBa₂(Cu_1–x Ti _x )₃O_z lowers the oxygen content and decreasesT _c, which is attributed to hole filling by Ti.     

Effect of Ca Substitution on the Superconductivity of La2.5Y0.5CaBa3(Cu0.88Fe0.12)7Oz

The structural and superconducting properties of single-phase La_2.5–y Y_0.5Ca_1+y Ba₃ (Cu_0.88Fe_0.12)₇O _z (LYCaBCuFe) (y= 0.0–1.0) compounds with triple perovskite structure are investigated using X-ray diffraction, resistivity, a.c. susceptibility, and oxygen content measurements. Increasing Ca substitution for La resulted in a decrease in unit cell axes and volume. T _c ^R=0 shows a marginal increase from 31 K to 37 K for y = 0.0–0.21 and thereafter it decreases with increasing y leading to zero T _c ^R=0 at y 0.84. This shows that the suppression of T _c from 80 K to 31 K by Fe doping at x = 0.12 La_2.5Y_0.5CaBa₃(Cu_1–x Fe _x )₇O _z cannot be compensated by appropriate hole doping with Ca in LaYCaBCuFe.     

Partial substitution of Li for Cu in superconducting YBa2Cu3Oy

0.33–33% of the Cu in superconducting YBa₂Cu₃O _y has been replaced by Li (i.e.,x=0.01–1 in single-phase or nominal YBa₂Cu_3?x Li_xO_y). X-ray diffraction powder patterns remain the same as for YBn₂Cu₃O _y , with identical patterns up to about 17% substitution (i.e.,x=0.5). At higher percentages an additional phase appears. Electrical conductivity measurements indicate a small elevation ofT _c at low Li content. Starting at about 5% Li (x=0.15),T _c declines progressively and its width increases asx is raised.     

Specific heat of the high-Tc oxide superconductors

We review the specific heat measurements on La₂CuO₄, La_2–xM_xCuO₄ (M = Ca, Sr, and Ba), YBa₂Cu₃O₇, and the Bi-Ca-Sr-Cu-O and Tl-Ca-Ba-Cu-O systems. Tables of properties derived from the data are presented. Results on RBa₂Cu₃O₇ (R=rare earth elements other than Y) are summarized, as are results on YBa₂(Cu_3–xM_x)O₇ (M=Zn, Cr, Fe, or Ni). The difficulties of analyzing the specific heat data, and specifically the separation of the contributions associated with magnetic impurities, are discussed. It is tentatively concluded that the data nearT _c are consistent with BCS theory, although they show evidence of fluctuation effects. It is also concluded that the low-temperature zero-field data on a majority of the high-T _c oxide superconductors provide evidence of anintrinsic term that is proportional toT, a result that is inconsistent with a gap in the electronic density of states.     

Enhancement of Pinning Role by Nonstoichiometry in YBa2Cu3O7?y Superconductors

Considerably improved flux pinning and critical current density J c values have been achieved in Y-deficient Y-123 superconductors by directional solidification in air. In comparison with the regular Y-123 composition, Y-deficient one also has an orthorhombic structure and Y-123 main crystal phase remains in it. Whereas with the shortage of Y, Y_1–x Ba₂Cu₃O_7–y can be regarded as (YBa₂Cu₃)_1–x O_7–t(Ba₂Cu₃) _x O _t–y or (YBa₂Cu₃O_7–z )( _x ^YO _z–y ), so there may develop several kinds of microstructure defects as pinning sites in the system, such as highly dense, fine-scale, and faultlike defects, as well as localized superstructure, which are able to induce the increasing in flux pinning and J c values in higher external magnetic fields. This kind of simple nonstoichiometric route could lead to a commercial technique for flux-pinning enhancement in Y-123 bulk materials.     

Investigations of Bi substitution in NdBa2Cu3Oy

Attempts to substitute Bi for Nd in orthorhombic NdBa₂Cu₃O _y , prepared in air or oxygen at about 950°C led instead to formation of Ba₂NdBiO₆, a new cubic compound witha=0.8703 nm. The possibility was then explored of preparing superconducting (Nd_1–x Bi _x )Ba₂Cu₃O _y , by first forming the tetragonal phase at 880–950°C in nitrogen or argon followed by reheating in oxygen or air at 250–500°C in order to insert the additional oxygen required to yield the orthorhombic form while avoiding oxidation of Bi³⁺ to Bi⁵⁺. X-ray diffraction studies, electrical conductivity measurements, and thermogravimetric analysis of products indicate that Bi does not enter the NdBa₂Cu₃O _y , lattice in either the tetragonal or the orthorhombic phase. Ba₂NdBiO₆ clearly forms on reheating in oxygen or air even at low temperatures, and evidence is presented that a poorly crystallized oxygen-deficient form of this compound is already present prior to the reheating.     

Magnetization and Susceptibility Studies on BaZrO3-Doped YBa2Cu3O7 ? x Bulk Superconductors

We studied the YBa₂Cu₃O_{7 – x} bulk superconductor doped with BaZrO₃ up to 50 wt.%, obtained by solid-state reaction powder technology. From DC magnetization loops and low frequency AC susceptibility measurements we determined the influence of the BaZrO₃ doping level on the critical temperature, critical current density, field for full penetration, and intergrain lower critical field. The results show that even high content of BaZrO₃ does not lead to degradation of the superconducting properties of bulk YBa₂Cu₃O_{7 – x} .     

d-Hole localization and the suppression of superconductivity in YBa2(Cu1-xZnx)3O7?y

The temperature and Zn concentration dependence of the electrical resistivity, specific heat, magnetic susceptibility, and electron paramagnetic resonance (EPR) spectra of YBa₂(Cu_1–x Zn _x )₃O_7–y withy0.1 has been measured forx0.16. In addition, the temperature and field dependence of the magnetization has been measured for 2<T<300K and 0<H<9.0T, along with the temperature and quasihydrostatic pressure dependence of the electrical resistivity for selected samples for 0<P<13 GPa. The substitution of Zn for Cu in YBa₂Cu₃O_7–y causes a rapid and nearly linear depression of the superconducting transition temperature,T _c , withT _c going to 0 K forx 0.10. YBa₂(Cu_1–x Zn _x )₃O_7–y retains the YBa₂Cu₃O_7-y orthorhombic structure forx0.16 for both the superconducting and nonsuperconducting samples. Initially, the unit cell volume increases nearly linearly with Zn content; however, an abrupt change occurs in the vicinityx=0.8–0.10. Forx<0.10, the temperature dependence of the electrical resistivity,(T), is metallic-like (d/dT>0) and increases gradually with increasing Zn content. However, forx 0.10,(T) becomes semiconductor-like, with a very rapid increase of the resistivity with increasingx. The electrical resistivity, magnetic susceptibility, EPR spectra, and specific heat all indicate that thed-holes associated with the Cu ions become localized in the nonsuperconducting phase,x>-0.10.     

The Underdoped Region of the Phase Diagram of YBa2Cu3O6+x

Here we present a reviewed phase diagram of the high-T _c superconducting YBa₂Cu₃O_{6+ x} compound, finely mapped in the strongly underdoped region (0 < x < 0.5), from the pure antiferromagnetic state to the superconducting regime. The Neèl and spin freezing temperatures have been measured by μSR experiments while the hole density per Cu atom in the CuO₂ planes has been determined from the resistive T _c and from Seebeck coefficients at 290 K. The phase diagram is discussed in comparison to those of La_{2− x} Sr _x CuO₄ and Y_{1− x} Ca _x Ba₂Cu₃O₆ cuprate systems.     

Transformation of the YBa2Cu3Ox superconducting phase to an insulator-nonsuperconducting phase

Three YBa₂Cu₃O _x samples (A, B, and C) were prepared under similar conditions. The starting materials were Y₂O₃ (99.99%), CuO (99.999%), and BaCO₃ (99.999%). All the specimens demonstrated a Meissner effect at liquid-nitrogen temperature. From temperature-dependent resistivity measurements, theT _c for the three samples was found to be aroundT _c =93 K, in agreement with other reports [1].     

Investigation of Magneto-Resistance Behavior in High Pulsed Magnetic Fields up to 35 T of YBa2Cu3O x and YBa2Cu3O x (5% Ag-doped) Thick Films Near 77 K

We investigated the influence of pulsed magnetic fields of up to 35 T on thick film samples of YBa₂Cu₃O _x (x<6.8) and YBa₂Cu₃O _x (5% Ag-doped), produced from powders on which electromagnetic separation had been performed. It was discovered, that subjecting the thick film samples of YBa₂Cu₃O _x to 10 pulses of a cyclic pulsed magnetic field of 32 T had the effect of significantly increasing T _c . The films had an oxygen deficit of 6.6–6.8%. Initially, T _c was 74 K. After the treatments by the strong pulses of magnetic fields, T _c had increased to 80 K. On the other hand, in YBa₂Cu₃O _x (5% Ag), the processing by strong pulsed magnetic fields will lead to dynamic mechanic stresses, which will increase the amount of tetragonal phases and lead to a lower temperature of the superconductivity transition.     

Solution-sol-gel processing of superconductors

Bulk materials and thin films of pure and homogeneous YBa₂Cu₃O_7−x and Bi₂Sr₂CaCu₂O_8+x compounds were prepared by a nanocomposite solution-sol-gel (SSG) method. The superconducting oxides of YBa₂Cu₃O_7−x and Bi₂Sr₂CaCu₂O_8+x were prepared at very low temperatures i.e. 750°C and 850°C, respectively by SSG method. Pellets sintered from these nanophasic sol powders showed sharp resistivity drops atT _c ∼ 90°K for YBa₂Cu₃O_7−x andT _c∼67°K for Bi₂Sr₂CaCu₂O_8+x . Thin films were prepared using triphasic sol of Y, Ba, Cu and tetraphasic sol of Bi, Sr, Ca and Cu on MgO and SrTiO₃ substrates. The triphasic sol coated on SrTiO₃ substrates and calcined at 800°C for 12h showed the formation of superconducting phase, YBa₂Cu₃O_7−x with preferred orientation along theC-axis. X-ray diffraction patterns of the Bi₂Sr₂CaCu₂O_8+x films on MgO substrate showed the formation of the superconducting phase with preferential orientation along the C-axis and the microwave absorption data as a function of temperature of this film revealed the onset temperature to be 90°K.     

500–600 K Dilatation Anomaly and Tc Increase in YBa2Cu3Ox

YBa₂Cu₃O _x bulk ceramics have been simultaneously investigated by the thermal expansion and the acoustic emission methods in the 500–600 K temperature range. An error of the differential dilatometer does not exceed 10^–7. At T = 555 K, the dilatation anomaly accompanied by the acoustic emission has been observed and measured. Based on this measured anomaly, a value of c = –0.003 m has been determined. And based on this c size the stoichiometric coefficient x = 7.01 has been calculated too. The possible mechanism for T _c increase in YBa₂Cu₃O _x as a result of closing b axis by the absorbed oxygen atoms during the samples' heating through 500–600 K has been discussed.     

Superconducting transition temperatures in the Ru-1232 system, RuSr2(Gd1? x Ln x Ce1.8Sr0.2)Cu2O z (Ln = Sm, Dy, and Ho)

We have investigated effects of the lanthanide element Ln and the composition changes on the superconducting transition temperatureT _c in the Ru-1232 system, RuSr₂(Gd_1−x Ln _x Ce_1.8Sr_0.2)Cu₂O _z (Ln = Sm, Dy, and Ho). At first, in the case of the samples with Ln = Sm among almost the single 1232 phase samples, the values of the superconducting onset temperatureT _co are almost the same forx=0.00−0.15, and each of the lattice parametersa andc is almost constant. While, in each of the cases of the samples with Ln = Dy and Ho, the sample withx=0.05 shows the maximum values for both the superconducting onset temperatureT _co and the zero resistivity temperatureT _cz. Especially for the sample with Ln = Dy, the values ofT _co andT _cz are 18.5 and 6.5 K, respectively. These are higher than those of the mother sample of RuSr₂(GdCe_1.8Sr_0.2)Cu₂O _z . Moreover, from variations ofT _co, lattice parameters ofa andc in the RuSr₂(Gd_1−x Dy _x Ce_1.8Sr_0.2)Cu₂O _z system as a function of Dy contentx, the relationship between the superconducting transition temperature and the lattice parameters in the present system are investigated.     

Chemical solution deposition of YBa2Cu3O7−x coated conductors

At present, the development of superconducting YBa₂Cu₃O_7−x coated conductors attracts much attention due to their enormous application potential in electric power systems. Worldwide research is focused on the investigation and improvement of buffer materials and YBa₂Cu₃O_7−x superconducting properties as well as low-cost manufacturing processes in cooperation with industrial companies. Accordingly, chemical solution deposition has emerged as a highly competitive, versatile, and cost-effective technique for fabricating coated conductors of high performance. New chemical solution approaches are under development for buffer layer deposition. In order to achieve high critical current carrying YBa₂Cu₃O_7−x layers, the established trifluoroacetate route is favored. This paper reviews the most recent work on chemical solution deposition within the IFW Dresden while also considering achievements on this specific research topic worldwide.     

Charge-transfer in YBa2Cu3Ox

The charge-transfer hypothesis is shown to be inconsistent with data for YBa₂Cu₃O_x: (i) The two-step behavior ofT _c(x) (with jumps from zero to 60 K and then to 90 K) is not reflected as a similar, statistically significant two-step behavior in the bond-valence-sum charge of cuprate-plane Cu ions (as once believed), (ii) as a consequence of the law of conservation of charge, the derivatives of the layer charges with respect to oxygen contentx for both the Ba-O layers and the charge-reservoir Cu-O chains have the opposite signs to those predicted, and (iii) the charge-transfer observed for superconducting YBa₂Cu₃O_x is not sufficient to produce superconductivity, as demonstrated by insulating PrBa₂Cu₃O_x, which has virtually the same layer charges.     

Comparison of Superconductivity and Structure for YBa2Cu3Oy with Potassium and Sodium Doping

The nominal composition of YBa_2–x M _x Cu₃O _y (M = K, Na) cuprates with x 0.30 were synthesized by the standard solid-state reaction technique. X-ray diffraction (XRD) and the resistivity measurements were used to characterize the structure and the superconductivity of the doped cuprates. There was no impurity phase detected within the whole doping range. The structure of the main phase (123) has the orthorhombic with P _mmm symmetry. With increasing the content of dopants, the lattice constants and some other structural parameters are almost unchanged for M = K, whereas they changed for M = Na. The refined contents of dopants are consistent with that of the nominal ones. The zero resistance temperature T _c0 decreases sharply with the increase of the content of potassium in potassium-doped samples as x 0.20. For sodium-doped YBa_2–z Na _x Cu₃O _y cuprates, T _c0 varies very little. The difference in superconductivity depression may result from the shift oxygen, which transfers conducting carriers from Cu-O chains to Cu-O₂ sheets or the structural stress effect.