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Abstract In a recent study to probe the effect of the pinning efficiency of BaZrO₃(BZO) nanorods in BZO-doped YBa₂Cu₃O_7-x(BZO/YBCO) nanocomposite films, Ca diffusion from two Ca_0.3Y_0.7Ba₂Cu₃O_7-xspacers that form multilayers through alternative stacking with three BZO/YBCO layers was found to significantly enhance the pinning by approximately five folds at high magnetic fields (B) up to 9.0 T. This raises a question on the role of Ca diffused into the multilayer BZO/YBCO nanocomposite films. In order to answer this question, this work investigates the Ca_0.3Y_0.7Ba₂Cu₃O_7-xfilms of variable thickness in the range of 33-190 nm to understand whether the carrier over-doping induced by Ca substitution of Y would lead to enhanced pinning. In addition, the effect of the thicknesses of the constituent YBCO and Ca_0.3Y_0.7Ba₂Cu₃O_7-xlayers was also studied. Furthermore, the amount of Ca in Ca_0.3Y_0.7Ba₂Cu₃O_7-xspacers may be controlled by varying their thickness ranging from 1 nm to 10 nm. Our result suggests that the benefit of over-doping via Ca/Y substitution is minimal on pinning. In addition, the amount of Ca in the Ca_0.3Y_0.7Ba₂Cu₃O_7-xspacers indeed affects the Ca diffusion and hence pinning enhancement dramatically, which reduces as the spacer thickness is below 5 nm threshold. Above this threshold, the Ca diffusion is highly effective through large BZO/YBCO thicknesses up to 330 nm (total film thickness ~ 1 µm) and significantly enhanced pinning has been obtained in multilayer BZO/YBCO nanocomposites. For example, theI_cexceeds 650 A per cm-width at 20 K and 9.0 T when B//c, which is only ~13% lower than that at B//ab due to the intrinsic pinning. 

High critical current (Ic) in high magnetic fields (B) with minimal variations with respect to the orientation of the B field is demanded by many applications such as high-field magnets for fusion systems. Motivated by this, this work studies 6 vol. % BaZrO3/YBa2Cu3O7 (BZO/YBCO) multilayer nanocomposite films by stacking two 10 nm thick Ca0.3Y0.7Ba2Cu3O7 (CaY-123) spacers with three BZO/YBCO layers of thickness varied from 50 to 330 nm to make the total film thickness of 150–1000 nm. The Ca diffusion from the spacers into BZO/YBCO was shown to dramatically enhance pinning efficiency of c-axis aligned BZO nanorods, which yields high and almost thickness independent critical current density (Jc) in the BZO/YBCO multilayer nanocomposite films. Remarkably, enhanced Jc was observed in these multilayer samples at a wide temperature range of 20–80 K and magnetic fields up to 9.0 T. In particular, the thicker BZO/YBCO multilayer films outperform their thinner counterparts in both higher value and less anisotropy of Jc at lower temperatures and higher fields. At 20 K and 9.0 T, Ic is up to 654 A/cm-width at B//c in the 6% multilayer (1000 nm) sample, which is close to 753 A/cm-width at B//ab due to the intrinsic pinning. This result illustrates the critical role of the Ca cation diffusion into the YBCO lattice in achieving high and isotropic pinning in thick BZO/YBCO multilayer films. 

One-dimensional artificial pinning centers (1D-APCs) in YBa2Cu3O7-x nanocomposite films provide strong collective pinning at magnetic field B//c-axis. In this work, we reveal a 1D-APC/YBa2Cu3O7-x interface is preferred for high pinning efficiency of individual 1D-APCs including BaHfO3 and BaZrO3. The coherent 1D-APC/YBa2Cu3O7-x interface may be obtained via either growth of the nanocomposite films at optimal condition or Ca-diffusion to dynamically reduce the interface strain during the nanocomposite film growth. Interestingly, the high pinning efficiency of the 1D-APCs with coherent interfaces with YBCO not only lead to a high critical current density (Jc) in magnetic fields up to 9.0 T at H//c-axis but also enhanced Jc over a larger angular range when H is away from H//c-axis up to θ=60-80 degree than that in the case the interface is defective. This result suggests the importance of understanding and engineering the APC/YBCO interface for optimal pinning in nanocomposite films. 

Abstract This work examines the pinning enhancement in BaZrO 3 (BZO) +Y 2 O 3 doubly-doped (DD) YBa 2 Cu 3 O 7 (YBCO) nanocomposite multilayer (DD-ML) films. The film consists of two 10 nm thin Ca 0.3 Y 0.7 Ba 2 Cu 3 O 7-x (CaY-123) spacers stacking alternatively with three BZO + Y 2 O 3 /YBCO layers of 50 nm each in thickness that contain 3 vol% of Y 2 O 3 and BZO doping in the range of 2–6 vol%. Enhanced magnetic vortex pinning and improved pinning isotropy with respect to the orientation of magnetic field (B) have been achieved in the DD-ML samples at lower BZO doping as compared to that in the single-layer counterparts (DD-SL) without the CaY-123 spacers. For example, the pinning force density ( F p ) of ∼58 GNm −3 in 2 vol.% of DD-ML film is ∼110% higher than in 2 vol% of DD-SL at 65 K and B // c -axis, which is attributed to the improved pinning efficiency by c -axis aligned BZO nanorods through diffusion of Calcium (Ca) along the tensile-strained channels at BZO nanorods/YBCO interface for improvement of the interface microstructure and hence pinning efficiency of BZO nanorods. An additional benefit is in the considerably improved J c ( θ ) and reduced J c anisotropy in the former over the entire range of the B orientations. However, at higher BZO doping, the BZO nanorods become segmented and misoriented, which may change the Ca diffusion pathways and reduce the benefit of Ca in improving the pinning efficiency of BZO nanorods. 

Abstract Microstructural analysis of the BaZrO 3 (BZO)/YBa 2 Cu 3 O 7 (YBCO) interface has revealed a highly defective and oxygen deficient 2-3 nm thick YBCO column surrounding the BZO one-dimensional artificial pinning centers (1D-APCs). The resulting semi-coherent interface is the consequence of the ∼7.7% BZO/YBCO lattice mismatch and is responsible for the low pinning efficiency of BZO 1D-APCs. Herein, we report an interface engineering approach of dynamic Ca/Cu replacement on YBCO lattice to reduce/eliminate the BZO/YBCO lattice mismatch for improved pinning at a wide angular range of the magnetic field orientation. The Ca/Cu replacement induces a local elongation of the YBCO c-lattice near the BZO/YBCO interface, thereby ensuring a reduction in the BZO/YBCO lattice mismatch to ∼1.4% and a coherent BZO/YBCO interface. This has resulted in enhanced pinning at B//c-axis and a broad angular range of B-field orientation. For example, the 6 vol.% BZO/YBCO film with interface engineering exhibits F p ∼158 GN/m 3 at 65 K and B//c-axis, which is 440% higher than the ∼36.1 GN/m 3 for the reference 6% BZO/YBCO sample, and enhanced J c and F p in a wide angular range up to ∼ 80°. This result illustrates a facile scheme for engineering 1D-APC/YBCO interface to resume the pristine pinning efficiency of the 1D-APCs.