Polycrystalline samples of Nd18Li8Fe5O39 and Nd18Li8Co4O39 have been synthesized using a solid-state method and studied by a combination of neutron diffraction, direct and alternating current magnetometry, and, in the case of Nd18Li8Fe5O39, Mössbauer spectroscopy. Both compounds adopt a cubic structure (space group Pm3̅n, a0 ~ 11.9 Å) based on intersecting (111) chains made up of alternating octahedral and trigonal-prismatic coordination sites. the Fe4+ cations in Nd18Li8Fe5O39 are found on only the smaller of the two distinct octahedral sites in the structure; Fe3+ and Li+ are disordered over the larger octahedral site and the trigonal-prismatic site. the Nd3+ cations occupy sites between the chains. the smaller octahedral site is fully occupied by cobalt in Nd18Li8Co4O39, with 25% of the larger octahedral sites being vacant; Li+ is only found on the prismatic sites. Nd18Li8Fe5O39 shows spin-glass-like behavior with a spin-freezing temperature of 5.75 K, whereas Nd18Li8Co4O39appears to order antiferromagnetically at 2.3 K. in both cases, the magnetic coupling involves the Nd3+ sublattice.
S. E. Dutton et al., "Structural Chemistry and Magnetic Properties of Nd₁₈Li₈Fe₅O₃₉ and Nd₁₈Li₈Co₄O₃₉: the Interplay of Cation and Spin Ordering," Inorganic Chemistry, American Chemical Society (ACS), Jan 2008.
The definitive version is available at http://dx.doi.org/10.1021/ic801529m
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