An x-ray diffraction study of the substitution of gallium in Tb 2Fe17 to form the Tb2Fe17-xGax solid solutions indicates that the compounds adopt the rhombohedral Th2Zn17 structure. The unit cell volume and the a-axis lattice parameter increase linearly with increasing gallium content. The c-axis lattice parameter increases linearly from x=0 to 6 and then decreases between x=7 and 8. Magnetic studies show the Curie temperature increases by ~150° above that of Tb2Fe17 to reach a maximum between x=3 and 4, and then decreases with further increases in x. Neutron diffraction studies of Nd2Fe15Ga2 and Tb 2Fe17-xGax, with x equal to 5, 6, and 8, indicate that the gallium completely avoids the 9d site, occupies the 6c "dumbell" site only at high values of x and strongly prefers the 18f site at high values of x. The magnetic neutron scattering indicates both that the terbium sublattice magnetization couples antiferromagnetically with the iron sublattice and that there is a change in easy magnetization direction from planar to axial with increasing gallium concentration. This change in easy magnetization direction is explained in terms of a sign reversal of the second-order crystal field parameter, A02, the most important parameter responsible for determining the terbium sublattice anisotropy. The Mössbauer effect spectra indicate a larger room-temperature average hyperfine field at the iron site in the Tb2Fe 17-xGax solid solutions than in several related R 2Fe17 compounds. The large observed increase in the isomer shift with increasing gallium content results from interatomic charge transfer and intraatomic s-d charge redistribution in the presence of gallium.
Z. B. Hu et al., "A Magnetic, Neutron Diffraction, and Mössbauer Spectral Study of Nd₂Fe₁₅Ga₂ and the Tb₂Fe₁₇₋ₓGaₓ Solid Solutions," Journal of Applied Physics, vol. 76, no. 1, pp. 443-450, American Institute of Physics Publishing LLC, Jul 1994.
The definitive version is available at https://doi.org/10.1063/1.357094
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© 1994 American Institute of Physics Publishing LLC, All rights reserved.
01 Jul 1994