Magnetic and Structural Properties of Rapidly Quenched Tetragonal Mn3-xGa Nanostructures

Nanostructured Mn3-x Ga ribbons with x = 0, 0.4, 0.9 and 1.1 were prepared using arc-melting, melt-spinning and annealing. As-spun samples crystallized into hexagonal D0(19) and cubic L2(1) Heusler crystal structures based on the concentration of Mn in Mn3-xGa. Upon vacuum-annealing the samples at 4...

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Published in:IEEE transactions on magnetics Vol. 49; no. 7; pp. 3277 - 3280
Main Authors: HUH, Y, KHAREL, P, SHAH, V. R, KRAGE, E, SKOMSKI, R, SHIELD, J. E, SELLMYER, D. J
Format: Conference Proceeding Journal Article
Language:English
Published: New York, NY Institute of Electrical and Electronics Engineers 01-07-2013
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Summary:Nanostructured Mn3-x Ga ribbons with x = 0, 0.4, 0.9 and 1.1 were prepared using arc-melting, melt-spinning and annealing. As-spun samples crystallized into hexagonal D0(19) and cubic L2(1) Heusler crystal structures based on the concentration of Mn in Mn3-xGa. Upon vacuum-annealing the samples at 450 degrees C for about 50 hours, both the hexagonal and cubic structures transformed into a tetragonal D0(22) structure. High-temperature x-ray diffraction and high-temperature magnetometry showed that the samples with low Mn content (Mn-1.9 Ga and Mn-2.1 Ga) retain their tetragonal structure up to 850 K but the samples with high Mn concentrations (Mn-2.6 Ga and Mn-3.0 Ga) undergo a structural phase transition from tetragonal to hexagonal phases around 800 K. The magnetic properties of Mn3-x Ga ribbons were very sensitive to Mn concentration, where the magnetization and anisotropy energy increased and the coercivity decreased as x increased from 0 to 1.1. Although the Curie temperatures of Mn-2.6 Ga and Mn-3.0 Ga samples could not be determined because of the structural phase transition, the Curie temperature decreased with increasing x in Mn3-x Ga. The maximum magnetization of 57 emu/g (300 emu/cm(3)) and the coercivity of 6.5 kOe were measured in the Mn-1.9 Ga and Mn-3.0 Ga ribbons, respectively.
Bibliography:DE-AR0000046
USDOE Advanced Research Projects Agency - Energy (ARPA-E)
ISSN:0018-9464
1941-0069
DOI:10.1109/TMAG.2013.2244856