The effect of carbon and rare earth oxide co-doping on the structural and superconducting properties of MgB₂
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Ojha, N.
Department of Physics, Indian Institute of Technology Roorkee, India
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Malik, Vivek Kumar
Department of Physics and Fribourg Centre for Nanomaterials-FriMat, University of Fribourg, Switzerland
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Singla, Rashmi
Department of Physics, Indian Institute of Technology Roorkee, India
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Bernhard, Christian
Department of Physics and Fribourg Centre for Nanomaterials-FriMat, University of Fribourg, Switzerland
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Varma, G. D.
Department of Physics, Indian Institute of Technology Roorkee, India
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Published in:
- Superconductor Science and Technology. - 2010, vol. 23, no. 4, p. 045005
English
Carbon (C) and rare earth oxide (REO) co-doped bulk polycrystalline MgB₂ samples with nominal compositions Mg1 − y(REO)y(B0.95C0.05)₂ (where y = 0.00, 0.01, 0.03, 0.05 and REO = Eu₂O₃ or Pr₆O₁₁) have been synthesized via a solid state reaction route. The XRD results reveal the presence of impurity phases EuB₆ in Eu₂O₃ and PrB₄ and PrB₆ in Pr₆O₁₁ co-doped samples along with the main hexagonal phase of MgB₂ and a small amount of MgO. The values of upper critical field (Hc2) and irreversibility field (Hirr), except Hc2 of y = 0.05 for Eu₂O₃, have been found to increase at all temperatures (<Tc) with increasing doping concentration of REO. Improvements in the values of critical current density (Jc) at 10 K for y = 0.01 of Eu₂O₃ and y = 0.01, 0.03 of Pr₆O₁₁ co-doped samples have been observed in high fields (>6.5 T) region. At 20 K enhancement in the high field (>6 T) Jc values for y = 0.01, 0.03 of Eu₂O₃ and y = 0.01 of Pr₆O₁₁ co-doped samples are also reported in the present work. The correlations between the structural characteristics and the observed superconducting properties of the co-doped samples are described and discussed in this paper.
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Faculty
- Faculté des sciences et de médecine
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Department
- Département de Physique
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Language
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Classification
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Physics
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License
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License undefined
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Identifiers
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Persistent URL
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https://folia.unifr.ch/unifr/documents/301444
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