TY - JOUR
T1 - Improvement of Jc and Hc2 in MgB2 superconductor with citric acid addition
AU - Zeng, R.
AU - Lu, L.
AU - Wang, J. L.
AU - Li, W. X.
AU - Shi, D. Q.
AU - Horvat, J.
AU - Dou, S. X.
PY - 2008
Y1 - 2008
N2 - This paper reports on the fabrication and characterization of citric acid (CA)-C6H8O7 added MgB 2superconductor. The relationships between microstructures, critical current density (Jc), critical temperature (Tc), upper critical field (Hc2), irreversibility field (Hirr), and normal state resistivity for 10 wt% C6H8O7added MgB2samples sintered at temperatures from 650°C to 950°C were systematically studied. A reduction in Tc and in lattice parameter a due to the C substitution and possible oxygen (O) effects occurs with C6H8O7 addition. Jc, H c2, and Hirr are significantly enhanced, however, with the addition of C6H8O7. All the samples exhibit Jc above 104A/cm2 at 5 K and 8 T. This value is higher than for the un-doped MgB2 by a factor of 9. The significant improvement in the superconducting properties is attributed to the lattice distortion due to the C and possible oxygen (O) substitution for boron, with the C and O coming from the decomposition of C6H8O 7.
AB - This paper reports on the fabrication and characterization of citric acid (CA)-C6H8O7 added MgB 2superconductor. The relationships between microstructures, critical current density (Jc), critical temperature (Tc), upper critical field (Hc2), irreversibility field (Hirr), and normal state resistivity for 10 wt% C6H8O7added MgB2samples sintered at temperatures from 650°C to 950°C were systematically studied. A reduction in Tc and in lattice parameter a due to the C substitution and possible oxygen (O) effects occurs with C6H8O7 addition. Jc, H c2, and Hirr are significantly enhanced, however, with the addition of C6H8O7. All the samples exhibit Jc above 104A/cm2 at 5 K and 8 T. This value is higher than for the un-doped MgB2 by a factor of 9. The significant improvement in the superconducting properties is attributed to the lattice distortion due to the C and possible oxygen (O) substitution for boron, with the C and O coming from the decomposition of C6H8O 7.
UR - http://handle.uws.edu.au:8081/1959.7/529147
U2 - 10.1088/1742-6596/97/1/012215
DO - 10.1088/1742-6596/97/1/012215
M3 - Article
SN - 1742-6596
SN - 1742-6588
VL - 97
JO - Journal of Physics: Conference Series
JF - Journal of Physics: Conference Series
IS - 1
M1 - 12215
ER -