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dc.contributor.advisorMichael J. Cima.en_US
dc.contributor.authorPatta, Yoda Ranteen_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Materials Science and Engineering.en_US
dc.date.accessioned2009-01-26T22:01:36Z
dc.date.available2009-01-26T22:01:36Z
dc.date.copyright2008en_US
dc.date.issued2008en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/44207
dc.descriptionThesis (S.M.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2008.en_US
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.descriptionIn title on t.p., double underscored "x" appears as subscript.en_US
dc.descriptionIncludes bibliographical references (p. 68-71).en_US
dc.description.abstractThe past two decades have seen advancements in high temperature superconducting cables for use in applications such as electrical transmission lines, propulsion systems, and mobile power generation systems. This work describes the development of a non-fluorine precursor solution for YBCO films with high critical current densities (Jc). An aqueous nitrate precursor solution system was selected from three possible precursor solution systems. It was further developed to produce YBCO films with Jc > 1 MA/cm2. Films up to ~800 nm thickness were made, and Jc > 1 MA/cm2 was obtained for films of over ~400 nm thickness. The developed aqueous solution contained a rheology modifier (hydroxyethyl cellulose / HEC), nitrates of Y, Ba, and Cu, and chelating agents (polyethylene glycol / PEG and sucrose). The total organic content was ~12 wt% of the entire solution, and the total cation concentration was ~0.7 M. The rheology modifying polymer determined the thickness of the deposited films. This allowed for the deposition of films with higher thickness than would be dictated by the total dissolved cations alone. A low temperature decomposition process was developed based on analyses of the chemical reactions that take place in the precursor films as they were heated. This process produced smooth and defect-free intermediate films that were stable under ambient conditions. These films were then heat treated to convert them into YBCO films. Recommendations for future work include further improvements to the precursor solution, including more effective chelating agents and possible alternative solvent systems. Intermediate films thicker than 2.5 [mu]m still tended to have surface defects.en_US
dc.description.abstract(cont.) Additional in-depth thermal analysis would further show how these defects develop, and adjustments to the decomposition process could be made accordingly. High resolution plan-view and cross-sectional microstructures of the films between the precursor state and their converted forms is recommended. These future studies will be valuable in further improving the performance and thickness of films derived from the non-fluorine precursor solution developed in this thesis.en_US
dc.description.statementofresponsibilityYoda Rante Patta.en_US
dc.format.extent71 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectMaterials Science and Engineering.en_US
dc.titleNon-fluorine precursor solutions for high critical current density REBa₂Cu₃O₇₋x̳ filmsen_US
dc.typeThesisen_US
dc.description.degreeS.M.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineering
dc.identifier.oclc277139561en_US


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