Please use this identifier to cite or link to this item:
|Title:||Structure, superconductivity and magnetic properties of mechanically alloyed Mg1 - xFexB2 powders with x = 0-0.4||Authors:||Gao, Y.D.
|Issue Date:||5-Apr-2004||Citation:||Gao, Y.D., Ding, J., Chen, Q., Rao, G.V.S., Chowdari, B.V.R. (2004-04-05). Structure, superconductivity and magnetic properties of mechanically alloyed Mg1 - xFexB2 powders with x = 0-0.4. Acta Materialia 52 (6) : 1543-1553. ScholarBank@NUS Repository. https://doi.org/10.1016/j.actamat.2003.12.001||Abstract:||Mechanical milling of Mg1-xFexB2 with x = 0-0.4 led to the formation of amorphous phase. For x = 0, the hexagonal MgB 2 phase was formed after a heat treatment at 450 °C or above with critical temperature Tc = 38-40 K. Fe-substituted MgB 2 phase was formed after annealing at 450 °C or above when x = 0.05, 0.1 and 0.2. Fe solubility in the MgB2 phase decreased with increasing annealing temperature, while lattice parameters (a and c) decreased. It has been found that critical temperature Tc increased with increasing annealing temperature. For Mg0.6Fe0.4B 2 powder, MgB2 phase could not be formed after crystallization. Single solid-solution MgB2 phase could be formed in Mg0.95Fe0.05B2 after annealing at 450 °C. This sample exhibited paramagnetic between 30 and 290 K with a high magnetic moment of μFe = 5.5-6.0μB. An anomaly (minimum in reciprocal magnetic susceptibility) was observed below 30 K, accompanied by magnetic splitting in Mössbauer spectroscopy. © 2003 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.||Source Title:||Acta Materialia||URI:||http://scholarbank.nus.edu.sg/handle/10635/98071||ISSN:||13596454||DOI:||10.1016/j.actamat.2003.12.001|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jun 12, 2021
WEB OF SCIENCETM
checked on Jun 4, 2021
checked on Jun 8, 2021
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.