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3D to 2D Magnetic Ordering of Fe3+ Oxides Induced by Their Layered Perovskite Structure
Author(s) -
Xabier Martínez de Irujo-Labalde,
Ulises Amador,
C. Ritter,
Masato Goto,
Midori Amano Patiño,
Yuichi Shimakawa,
Susana GarcíaMartín
Publication year - 2021
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.1c00529
Subject(s) - superexchange , octahedron , chemistry , antiferromagnetism , tetrahedron , crystallography , perovskite (structure) , spins , condensed matter physics , magnetic structure , polyhedron , square pyramid , magnetic moment , crystal structure , magnetization , magnetic field , geometry , physics , mathematics , quantum mechanics
The antiferromagnetic behavior of Fe 3+ oxides of composition RE 1.2 Ba 1.2 Ca 0.6 Fe 3 O 8 , RE 2.2 Ba 3.2 Ca 2.6 Fe 8 O 21 , and REBa 2 Ca 2 Fe 5 O 13 (RE = Gd, Tb) is highly influenced by the type of oxygen polyhedron around the Fe 3+ cations and their ordering, which is coupled with the layered RE/Ba/Ca arrangement within the perovskite-related structure. Determination of the magnetic structures reveals different magnetic moments associated with Fe 3+ spins in the different oxygen polyhedra (octahedron, tetrahedron, and square pyramid). The structural aspects impact on the strength of the Fe-O-Fe superexchange interactions and, therefore, on the Néel temperature ( T N ) of the compounds. The oxides present an interesting transition from three-dimensional (3D) to two-dimensional (2D) magnetic behavior above T N . The 2D magnetic interactions are stronger within the FeO6 octahedra layers than in the FeO4 tetrahedra layers.

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