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Microstructural analysis of the compatibility of solution deposited buffer layers with the TFA process for YBCO

Published online by Cambridge University Press:  18 March 2011

K. Salama
Affiliation:
Texas Center for Superconductivity, University of Houston, Houston, TX 77204
S. Sathyamurthy
Affiliation:
Oak Ridge National Laboratory, Oak Ridge, TN 37831
M. Mironova
Affiliation:
Texas Center for Superconductivity, University of Houston, Houston, TX 77204
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Abstract

In this paper, the feasibility of applying solution deposition processes for the fabrication of coated conductors has been explored. The crystal and chemical compatibility of the buffer layers processed using metalorganic decomposition with the Y123 deposition using the trifluoroacetate process has been studied. Two buffer layer materials have been used, namely, barium zirconate and strontium titanate. The measured superconducting properties of these conductors were correlated with the microstructure observed on these samples using SEM and cross-sectional TEM. In case of barium zirconate buffer layers, though there exists a very good structural and chemical compatibility between the buffer layer and the Y123, the presence of surface defects in the buffer layer causes compositional heterogeneity and randomly oriented grains in the Y123 film. This leads to poor superconducting properties. In case of strontium titanate buffer layers, due to the excellent crystal and chemical compatibility, and the absence of surface defects, high critical current densities (of the order of 106A/cm2 at 77K and self field) were obtained. However, TEM cross section studies reveals the presence of a significant portions of a-oriented Y123 crystallites which could lead to lower critical current densities. Further studies of the TFA process is required to eliminate the occurrence of a-oriented Y123 in the microstructure. This could lead to further improvements in the properties.

Type
Research Article
Copyright
Copyright © Materials Research Society 2001

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References

REFERENCES

[1] Iijima, Y., Tanabe, N., Kohno, O., Ikeno, Y., Appl. Phys. Lett., v61, p2231 (1992).Google Scholar
[2] Norton, D.P., Goyal, A., Budai, J.D., Christen, D.K., Kroeger, D.M., Specht, E.D., He, Q., Saffian, B., Paranthaman, M., Klabunde, C.E., Lee, D.F., Sales, B.C., and List, F.A., Science, v274, p755 (1996).Google Scholar
[3] Schwartz, R.W., Voigt, J.A., Tuttle, B.A., Payne, D.A., Reichert, T.L., and DeSalla, R.S., J. Mater. Res., v12, p444 (1997)Google Scholar
[4] Paranthaman, M., Shoup, S.S., Beach, D.B., Williams, R.K., and Specht, E.D., Mater. Res. Bull., v32, p1697 (1997).Google Scholar
[5] McIntyre, P.C. and Cima, M.J., J. Mater. Res., v9, p2219 (1994).Google Scholar
[6] Sathyamurthy, S. and Salama, K., Physica C 341, p2479 (2000).Google Scholar
[7] Sathyamurthy, S. and Salama, K., Supercond. Sci. Tech., v13, L1–L3 (2000).Google Scholar
[8] Sathyamurthy, S. and Salama, K., J. Supercond., v11, p545 (1998).Google Scholar
[9] Sathyamurthy, S. and Salama, K., Physica C 329, p58 (2000).Google Scholar
[10] McIntyre, P.C., Cima, M.J., and Roshko, A., J. Appl. Phys., v77, p5263 (1995).Google Scholar
[11] Solovyov, V.F., Weissman, H.J., Wu, L., Suenaga, M., and Feenstra, R., IEEE Trans. Appl. Supercond., v9, p1467 (1999).Google Scholar
[12] Smith, J.A., Cima, M.J., and Sonnenberg, N., IEEE Trans. Appl. Supercond., v9, p1531 (1999).Google Scholar