The system Nd-Fe-Sb: Phase equilibria, crystal structures and physical properties

Author(s)
Andrij Grytsiv, Peter Franz Rogl, Dariusz Kaczorowski, Herta Silvia Effenberger
Abstract

Phase equilibria within the isothermal section of the ternary system Nd-Fe-Sb were derived at 800 °C by using X-ray powder diffraction, light optical microscopy and electron probe microanalysis. Crystal structures of the ternary compounds Nd2Fe7-x Sb6-y (?2-orthorhombic), Nd2Fe5-x Sb10-y (?2-tetragonal) Nd3Fe3Sb7 (?3) and NdFeSb3 (?4) were determined by single crystal X-ray diffraction and by Rietveld X-ray powder data refinement. The phase ?2 was found to exhibit two modifications, orthorhombic (Nd2Fe7-x Sb6-y -type, S.G. Immm, a = 0.42632(6) nm, b = 0.43098(7) nm, c = 2.5823(3) nm) and tetragonal (La2Fe5-x Sb10-y -type, S.G. I4/mmm, a = 0.42897(2) nm, c = 2.5693(4) nm). Tetragonal and orthorhombic modifications form a crystallographic group-subgroup relation and are closely related to the Zr3Cu4Si6-type. Nd3Fe3Sb7 (?3) crystallizes with a unique structure type (S.G. P63/m, a = 1.31808(3) nm, c = 0.41819(3) nm), which is isopointal to the Cu10Sb3-type. NdFeSb3 (?4) adopts the LaPdSb3-type. Physical properties comprising magnetization, resistivity and specific heat were measured for RE2Fe5-x Sb10-y (RE = Ce, Nd), NdFeSb3 and Nd3Fe3Sb7. NdFeSb3 orders antiferromagnetically below 3.0 K due to the presence of magnetic moments on Nd sites. For the other compounds a more complex magnetic behaviour is observed at low temperatures that may be related to the contributions coming from both the rare earth and iron sublattices.

Organisation(s)
Department of Physical Chemistry, Department of Mineralogy and Crystallography
External organisation(s)
Polish Academy of Sciences
Journal
Intermetallics
Volume
18
Pages
2361-2376
No. of pages
16
ISSN
0966-9795
DOI
https://doi.org/10.1016/j.intermet.2010.08.037
Publication date
2010
Peer reviewed
Yes
Austrian Fields of Science 2012
104017 Physical chemistry, 105113 Crystallography, 103018 Materials physics
Portal url
https://ucrisportal.univie.ac.at/en/publications/191cdb54-df7a-4b52-92ab-f179bb2b567e