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.



Document Type

Article - Journal

Document Version

Final Version

File Type





© 2008 American Chemical Society (ACS), All rights reserved.

Full Text Link

Included in

Chemistry Commons