High-Pressure Synthesis of Double Perovskite Ba2NiIrO6: In Search of a Ferromagnetic Insulator
Author(s) -
Hai L. Feng,
Zheng Deng,
Carlo U. Segre,
Mark Croft,
Saul H. Lapidus,
Corey E. Frank,
Youguo Shi,
Changqing Jin,
David Walker,
M. Greenblatt
Publication year - 2020
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.0c03402
Subject(s) - ferromagnetism , antiferromagnetism , condensed matter physics , valence (chemistry) , materials science , perovskite (structure) , magnetization , octahedron , crystallography , crystal structure , chemistry , magnetic field , physics , organic chemistry , quantum mechanics
Double perovskite oxides with d 8 -d 3 electronic configurations are expected to be ferromagnetic from the Goodenough-Kanamori rules, such as ferromagnetic La 2 NiMnO 6 . In search of new ferromagnetic insulators, double perovskite Ba 2 NiIrO 6 was successfully synthesized by high-pressure and high-temperature methods (8 GPa and 1573 K). Ba 2 NiIrO 6 crystallizes in a cubic double perovskite structure (space group: Fm 3̅ m ), with an ordered arrangement of NiO 6 and IrO 6 octahedra. X-ray absorption near-edge spectroscopy confirms the nominal Ni(II) and Ir(VI) valence states. Ba 2 NiIrO 6 displays an antiferromagnetic order at 51 K. The positive Weiss temperature, however, indicates that ferromagnetic interactions are dominant. Isothermal magnetization curves at low temperatures support a field-induced spin-flop transition.
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