Pinning potential in thick PrBa2Cu3Ox/YBa2Cu3O7−δ quasi-multilayers

Using Pulsed Laser Deposition we have fabricated thick quasi-multilayers composed of incomplete layers of PrBa₂Cu₃O_x (PrBCO) nano-dots and layers of YBa₂Cu₃O_7?δ (YBCO). The number of such sequences was between 2 and 6, with the thickness of individual YBCO layers between 565 and 885 nm, and total thickness between 1.13 and 5.31 μm. For the thinner quasi-multilayer, DC magnetization studies showed an increase in the critical current density J_c at all fields in comparison with a pure YBCO reference sample, while the thicker samples showed an increased J_c only in high fields. We have also investigated the frequency dependence of J_c from AC susceptibility studies and found that the pinning potential is well described by a logarithmic dependence on current density. Pinning potentials in PrBCO/YBCO quasi-multilayers also proved to be higher than in the reference sample at high fields. From angle-dependent transport measurements we have found indications of strong pinning centres induced by the (PrBCO) nano-dots, both isotropic and c-axis correlated.     

Inducing self-assembly of Y2BaCuO5 nanoparticles via Ca-doping for improved pinning in YBa2Cu3O7−x

Different mechanisms may exists as a means to provide additional or specialized enhancement of existing nanoparticulate pinning in YBa₂Cu₃O_7?x (YBCO) thin films. In the particular case of Y₂BaCuO₅ (Y211) nanoparticles, Ca-doping of these nanoparticles via addition to the Y211 target material provides an additional increase to the J_c(H). YBCO + Y211 samples were created by pulsed laser deposition with alternating targets of YBCO with Y211 and Y211 doped with Ca. Initial indications suggest that this improvement in pinning results from some scattered short-ranged self-assembly of the nanoparticles into short nanocolumns.     

Quick screening for new flux pinning materials in YBCO films with the combinatorial-PLD method

An effective way to improve the superconducting properties in REBa₂Cu₃O_y (REBCO) films under a magnetic field is to dope artificial pinning centers (APC). The pinning performance depends on the content of the APC materials. Usually, the optimal APC content is explored by preparing films one at a time from the REBCO target using different APC material content, which is an extremely time-consuming process.The combinatorial-PLD (C-PLD) method allowed us to prepare films that continuously changed in composition across a single substrate. In this study, we used the C-PLD method to prepare BaSnO₃ (BSO)-doped YBCO films. The films were deposited on SrTiO₃ substrate using a fourth-harmonic Nd:YAG laser. From the results of the J_c–B curves at 77 K and B//c, the film that contained 3.2 vol.% of BSO exhibited the best pinning performance in this study. We showed that the C-PLD method was efficient for quick screening of the optimal APC content with only one deposition. We also used the C-PLD method to explore new APC materials, and proved that it can quickly evaluate the new APC materials Ba₃Cu₃In₄O₁₂ and BaTbO₃.     

Preparation of solution-based YBCO films with BaSnO3 particles

The YBCO films with BaSnO₃ (BSO) particles were prepared on LAO (0 0 1) substrates by metal organic deposition using trifluoroacetates (TFA-MOD) via introducing SnCl₄ powders into the YBCO precursor solution. It was found that with the increase of the SnCl₄ contents, the slower decomposition and higher temperature for nucleation during the reaction were requested compared to that of pure YBCO film. The YBCO films with different contents of Sn with dense surface and well c-alignment were obtained under optimized heat treatment, and the BaSnO₃ phases were detected by XRD analysis. Litter effect of BSO particles on the T_c and J_c values of YBCO films was found. All YBCO films with BSO particles had T_c values over 90 K and J_c values over 1 MA/cm². A significant enhancement of J_c was observed for YBCO films with BSO particles compared to that of pure YBCO film by the field dependence of J_c values. The best property was obtained for YBCO film with 6 mol.% Sn at 77 K under magnetic field. The results showed that the J_c value of YBCO film with 6 mol.% Sn was enhanced by a factor of 2 in 2 T, and over a factor of 10 beyond 4 T compared to that of pure YBCO film.     

High performance GdBa2Cu3O7−z film preparation by non-fluorine chemical solution deposition approach

Biaxially textured GdBa₂Cu₃O_7?z (GdBCO) films with T_c above 93 K have been prepared on (0 0 l) LaAlO₃ substrate by self-developed non-fluorine polymer-assisted chemical solution deposition (PA-CSD) approach. The GdBCO films show smooth and crack-free morphology. Many nanoscale particles with homogeneous distribution are observed in the GdBCO films, which have not been observed yet in the YBa₂Cu₃O_7?z (YBCO) films prepared by the same processing technique. Besides a high J_c (77 K, 0 T) of 2.28 MA/cm², the optimized GdBCO films show a better J_c–B behavior and an improved high-field J_c, compared to the YBCO films.     

Vortex pinning in bulk-processed Y–Ba–Cu–O with ZrO2 nano-particles: Optimum pinning center size

Crystalline defects on the nano-scale were successfully introduced into YBCO high-temperature superconductors (HTS) by ZrO₂ nanometer particles addition in order to strongly pin the quantized vortices. Three batches of ZrO₂ nano-particles with different particle size distributions were used. The corresponding mean nano-particle diameters are respectively, 287, 536 and 764 nm. Serving as artificial pinning centers (APC), non-superconducting nano-particles cause a remarkable enhancement of critical current density (J_c) at T = 77 K. This improvement has been shown to depend on the size of APC. The pinning strength of nano-particles inclusions has been found to be greater with wide size dispersed nano-particles. Our results indicate that pinning properties and vortex dynamics depend on the size of APCs. The introduction of APCs with controlled size is indispensable to achieve a high J_c.     

Effects of nanoscale defects on critical current density of (Y1−xEux)Ba2Cu3O7−δ thin films

In pulsed laser deposition of YBa₂Cu₃O_7?δ films, defect introduction into the films tends to anisotropically improve the pinning along the H||c direction due to the columnar growth mode of the process. In Eu-substituted samples, however, even though an increase in critical current density (J_c) in the H||c direction was observed for low fields (H = 0.2 T), the improvement was more notable for the H||ab-plane at both low and higher fields. Herein we present detailed TEM microstructural studies to understand these new trends in J_c(H), which are markedly different than flux pinning increases achieved with other methods, for example, with nanoparticle additions. Threading dislocations, observed in the Eu-substituted samples along the c-axis, account for J_c enhancement with H||c at low field. The enhanced ab-planar pinning in the Eu-substituted samples is attributed to the extensive bending of the {0 0 1} lattice planes throughout the film, and the crystal lattice defects with excess Cu–O planes, that were effective in increasing the J_c for H||ab at both low and high fields.     

Stable barium compounds in YBa2Cu3Oy superconductors

The stability of various amounts of Ba₃Cu₃In₄O₁₂ (334) or BaTbO₃ (BTO) in a sintered YBa₂Cu₃O_y (YBCO) matrix was examined. Samples with added 334 or BTO exhibited critical temperatures (T_c) above 90 K for up to 20 vol.% addition and improved critical current densities (J_c) under a magnetic field. X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray (EDX) analysis indicated that 334 and BTO did not react with the YBCO matrix under the sintering conditions used. The normalized J_c under a magnetic field of 1 T reached a maximum at 14 vol.% of 334 addition and 20 vol.% BTO addition. YBCO thin films with added BTO showed a gradual decrease in the T_c with increasing BTO content. YBCO films with added 334 showed a constant T_c of 87 K up to a 334 content of 4 vol.%.     

Effects of tin-compounds addition on Jc and microstructure for YBCO films

Tin-compounds were doped into YBa₂Cu₃O_7−δ (YBCO) films as pinning centers to enhance J_c in magnetic fields. YBCO films were grown by a metal organic deposition process using tri-fluoroacetates starting solutions. Tin-acetylacetonate salts were then dissolved into the starting solution as pinning centers. J_c of the YBCO films with tin-acetylacetonates were enhanced in all magnetic field angles. Transmission electron microscopy (TEM) and TEM-EDS (Energy Dispersive X-ray Spectroscopy) observations revealed the existence of tin-compound particles with the size of about 30 nm in the YBCO film. These nano particles were distributed randomly in the film and were considered to act as 3-dimentional pinning centers.     

Alumina nano-inclusions as effective flux pinning centers in Y–Ba–Cu–O superconductor fabricated by seeded infiltration and growth

The YBa₂Cu₃O_7?x (Y123) textured bulk superconductors with various amounts of nanometer alumina particles were fabricated by a seeded infiltration and growth process. The addition of nanometer alumina was found to be effective for an improvement of the superconducting properties. The critical current density (J_c) values were increased twice in self field with a slight addition amount of nanometer alumina particles (maximum J_c at 0.01 wt.% alumina addition). The present work suggests that the use of insulating inclusions in the nanometer sub-scale can stabilize the flux-line lattice and greatly enhance the pinning capabilities of the infiltrated samples. No refinement of Y211 particles was observed with alumina addition. The J_c improvement by nanometer alumina inclusions is likely rendered to the insulating nano-pinning centers that have been successfully embedded into superconducting Y123 matrix. On the other hand, we examined the effect of the pinning centers size on the superconducting properties of infiltrated YBCO bulk samples. To this effect insulating nano-pinning centers with two different size distributions has been successfully incorporated within YBCO matrix of bulk superconductor by slightly doping with nano-particle alumina dispersions. Two alumina nano-particle dispersions with mean size diameters of about 20 nm and 130 nm were used. It was shown that the size of the pinning centers can affect considerably the J_c performances and the pinning mechanism.     

Enhancement of the critical current density in YBCO/Ag composites

YBa₂Cu₃O_7 + xAg?(x = 0.0, ?5.0, ?15.0 and 20 wt%) composite samples have been prepared by the solid state reaction method. The changes in structure are confirmed from the X-ray diffraction analysis and SEM measurements. The critical current density is calculated using Bean's formula from the magnetization measurement. We find that the addition of silver in YBCO enhances the critical current density (?J_C) by a factor of nearly six (for 15% Ag) in comparison to pure YBCO. Enhancement of the pinning force (F_P) by a factor of ten is also reported. The enhancement in ?J_C is investigated over a wide range of magnetic fields. These significant changes in ?J_C and F_P are attributed to the presence of Ag particles as efficient artifical pinning centers in YBCO.     

Preparation and properties of Y1−xHoxBa2Cu3O7−δ thin films by TFA-MOD method

Y_1?xHo_xBa₂Cu₃O_7?δ (x = 0, 0.1, 0.2, 0.3, 0.4, 0.5) thin films were prepared on LaAlO₃ (0 0 1) substrates by trifluoroacetate metal organic deposition (TFA-MOD) without change of the processing parameters. The highest J_c was attributed to the sample of Y_0.6Ho_0.4Ba₂Cu₃O_7?δ thin film, whose critical current density is about 1.6 times as compared to that of YBa₂Cu₃O_7?δ thin film at 77 K and self field. The flux pinning type was not varied with Ho substitution and can be attributed to δl pinning model, which is attributed to the close ionic radius between the Y³⁺ and Ho³⁺ ions. The improvement of J_c by Ho substitution without change of the processing parameters will provide an effective route to enhance the J_c of YBCO-based thin films using TFA-MOD method.     

YBCO films buffered by pyrochlore Nd2Mo2O7 layer on YSZ substrates by chemical solution deposition

A chemical solution deposition process was used to grow epitaxial Nd₂Mo₂O₇ (NMO) buffer layers on YSZ substrates to produce YBa₂Cu₃O_7?δ (YBCO) coated conductors. The NMO precursor solution prepared using metal acetylacetonates was spin-coated onto single crystal YSZ substrate of 10 mm × 10 mm in size at 3000 rpm for 30 s and heat-treated at 1000 °C for 2 h in Ar after calcinated at 550 °C for 1 h. The YBCO film was deposited by TFA-MOD route on top of the NMO/YSZ architecture. The phase purity and the crystalline orientation of NMO and YBCO films were evaluated by X-ray diffraction (XRD). Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used to observe their microstructure and their surface roughness. The critical current density (J_c) of YBCO film on NMO/YSZ is 1.8 MA/cm² at 77 K in self-field, which indicates that the Nd₂Mo₂O₇ is a potential buffer for YBCO coated conductor.     

Effects on Jc of pinning center morphology for multiple-in-line-damage in coated conductor and bulk,melt-textured HTS

The properties of discontinuous aligned pinning centers (PCs) created by high-energy heavy-ions are compared for bulk melt-textured and coated conductor HTS. Properties of PCs, which increase J_c (pinning potential and entanglement), and negative properties which decrease J_c (e.g., decreased T_c and percolation paths) are evaluated. Mechanisms are proposed to explain the very large increases in J_c resulting from multiple-in-line-damage (MILD) compared to continuous columnar pinning centers (CCPC). In particular, a mechanism which results in fluxoid entanglement, even for parallel (unsplayed) PCs, is discussed. The same mechanism is found to also account for restoration of much of the pinning potential expected to be lost due to the gaps in MILD PCs. It also accounts for the fact that at high fluence, J_c increases as fluence is increased, instead of decreasing as expected. The very low self-field in coated conductor permits separation of the negative and positive effects of PCs. It is found that parameters developed to quantify the negative effects in bulk melt-textured YBCO, by 63 GeV U²³⁸ ions, successfully describe damage to 2.1 μm thick coated conductor by 1 GeV Ru⁴⁴ ions. Coated conductor at 77 K and self-field is generally known to have J_c about 100 times that of melt-textured YBCO. However, at 77 K and applied field of 1 T, when both forms of HTS are processed with comparable numbers of near-optimum MILD PCs, the difference in J_c is reduced to a factor of 1.3–2. Whereas J_c for melt-textured YBCO increased sharply, by a factor of up to 16.8 for high-fluence MILD PCs, J_c in coated conductor increased by a smaller factor of 2.5–3.0. Nevertheless, 2.1 μm thick coated conductor, with near-optimum MILD PCs, exhibits J_c = 543 kA/cm² at 77 K and applied field of 1.0 T, and I_c = 114 A/cm-width of conductor. This is the highest value we find in the literature. The phenomenology developed indicates that for optimum MILD PCs in coated conductor, J_c ～ 700 ± 70 kA/cm² should be achievable at 77 K, 1.0 T.     

Thickness dependence of Ic and Jc of LTG-SmBCO coated-conductor on IBAD-MgO tapes

We have reported SmBa₂Cu₃O_y (SmBCO) films on single crystalline substrates prepared by low-temperature growth (LTG) technique. The LTG-SmBCO films showed high critical current densities in magnetic fields compared with conventional SmBCO films prepared by pulsed laser deposition (PLD) method. In this study, to enhance critical current (I_c) in magnetic field, we fabricated thick LTG-SmBCO films on metal substrates with ion-beam assisted deposition (IBAD)-MgO buffer and estimated the I_c and J_c in magnetic fields.All the SmBCO films showed c-axis orientation and cube-on-cube in-plane texture. T_c of the LTG-SmBCO films were 93.1–93.4 K. J_c and I_c of a 0.5 μm-thick SmBCO film were 3.0 MA/cm² and 150 A/cm-width at 77 K in self-field, respectively. Those of a 2.0 μm-thick film were 1.6 MA/cm² and 284 A/cm-width respectively. Although I_c increased with the film thickness increasing up to 2 μm, the I_c tended to be saturated in 300 A/cm-width. From a cross sectional TEM image of the SmBCO film, we recognized a-axis oriented grains and 45° grains and Cu–O precipitates. Because these undesired grains form dead layers, I_c saturated above a certain thickness. We achieved that I_c in magnetic fields of the LTG-SmBCO films with a thickness of 2.0 μm were 88 A/cm-width at 1 T and 28 A/cm-width at 3 T.     

Flux pinning in columnar-structured and single crystalline MgB2 films

We have investigated the flux pinning effect of columnar grain boundary in columnar-structured and single crystalline MgB₂ films. The MgB₂ films with columnar structure showed much higher J_c than that of single crystalline thin film, and sample having smaller grain size had a higher J_c in high magnetic fields. At 5 K, the MgB₂ film with grain size of 460 nm showed an abnormal double-peak behavior in pining force density, F_p(B), caused by competition of different types of pinning sites, such as planar defects and point defects. Field dependences of F_p in columnar-structured films suggest that the columnar grain boundary is a strong pinning source in the MgB₂ film and it plays a crucial role in enhancing J_c over a wide range of magnetic fields and temperatures.     

Aqueous polymer–nitrate solution deposition of YBCO films

High critical current density YBa₂Cu₃O_7?x (YBCO) films were prepared by solution deposition of aqueous non-fluorine precursors. Non-fluorine polymer-assisted deposition (PAD) processes utilizing rheology modifiers and chelating agents were used to produce 50 nm films with a critical current density (J_c) over 3 MA/cm² and 400 nm films with J_c > 1 MA/cm²_. T_c measurements indicated that films have T_c values near 90 K. The total heat treatment time to produce these high performance films was less than 4 h. Rheology modifiers such as polyvinyl alcohol (PVA) and hydroxyethyl cellulose (HEC) were used to increase the thickness of deposited films independent of the solution cation concentration. Chelating agents such as polyethylene glycol (PEG) and sucrose increased the barium ion solubility. Nitrate crystallization during deposition was controlled through rapid drying with vacuum and coating with hot solutions.     

Reel-to-reel fabrication of meter-long YBCO coated conductor

YBa₂Cu₃O_7?δ (YBCO) superconductors were coated on the CeO₂/YSZ/Y₂O₃ buffered Ni-5at%W tapes by a reel-to-reel pulsed laser deposition (PLD). The process of a multi-layer deposition of YBCO film was explored. X-ray diffraction texture measurements showed good both in-plane and out of plane crystalline orientations in YBCO films. The average values calculated at a full width at half maximum (FWHM) of the peaks from phi-scans (φ) and omega (ω) scans for one meter-long YBCO tape were 7.49° and 4.71°, respectively. The critical current (I_c) was over 200 A/cm-width at 77 K and under self-field for meter-long YBCO tape. The critical transition temperature of the YBCO tape was typically as 90.1 K with 0.5 K transition widths.     

Epitaxial growth of Ce2Y2O7 buffer layers for YBa2Cu3O7−δ coated conductors using reel-to-reel DC reactive sputtering

Biaxially textured Ce₂Y₂O₇ (CYO) films were deposited on Ni–5at.%W (Ni–5W) tapes by a DC reactive sputtering technique in a reel-to-reel system. Subsequent YBa₂Cu₃O_7?δ (YBCO) films were prepared using pulsed laser deposition leading to a simplified coated conductor architecture of YBCO/CYO/Ni–5W. X-ray diffraction measurements revealed an epitaxial growth of the CYO buffer layer with a texture spread down to 2.2° and 4.7° for the out-of-plane and in-plane alignment, respectively. Microstructural investigations showed a dense, smooth and crack-free surface morphology for CYO film up to a thickness of 350 nm, implying an effective suppression of cracks due to the incorporation of Y in CeO₂. The superconducting transition temperature T_c of about 90 K with a narrow transition of 0.8 K and the inductively measured critical current density J_c of about 0.7 MA/cm² indicate the potential of the single CYO buffer layer.     

Reduced crystallization time of YBCO in a fluorine-free MOD process using uv-lamp irradiation

We have studied the crystallization time dependence of the epitaxial YBCO films (t = 0.8 μm) grown on CeO₂-buffered SrTiO₃ substrates by fluorine-free metal–organic deposition using uv-lamp irradiation (uv-MOD). As increasing the time (T₀) for heat treatment at the reaction temperature (760 °C) from 0 to 90 min, J_c and the YBCO 0 0 l XRD intensity are steeply increased and reach their maximum values at T₀ = 10 min. This suggests that the heat treatment required for YBCO crystallization is significantly shortened in uv-MOD compared to conventional all-pyrolytic F-free MOD processes, which consume T₀ = 90–150 min for crystallizing 0.4–0.5-μm-thick films. Scanning electron microscope measurement revealed a drastic change in surface morphology between T₀ = 8 and 10 min, showing a good correspondence to the J_c and XRD data which suggest that the epitaxial growth reaches the film surface at the very early stage in the heat treatment.