Authors
Cierra J Foster, Jie Xiong, Matt Boswell, Weiwei Xie, Maxim Avdeev, Patrick M Woodward
Published in
Inorganic chemistry. Jul 09, 2025. Epub Jul 09, 2025.
Abstract
Polycrystalline samples of Ba3Cr2ReO9 and Ba2CrReO6 were synthesized using solid-state methods and characterized using laboratory X-ray powder diffraction (XRPD), magnetometry, specific heat, and variable temperature neutron powder diffraction (NPD). Ba3Cr2ReO9 and Ba2CrReO6 both crystallize in the 6H hexagonal structure with space group symmetry P63/mmc. The transition metal ions in Ba3Cr2ReO9 are ordered with Re6+ ions preferentially occupying the octahedra that share corners, and Cr3+ ions preferentially occupying sites in the face-sharing bioctahedra. Though there is a small amount of antisite mixing between the two ions. Ba2CrReO6 adopts a very similar crystal structure with a substantially higher fraction of Re5+ in the face-sharing bioctahedra. Both Ba3Cr2ReO9 and Ba2CrReO6 exhibit long-range antiferromagnetic ordering. The magnetic structures feature antiferromagnetic Re-O-Cr superexchange coupling through shared octahedral corners and antiferromagnetic Cr-Cr (or Cr-Re) direct exchange interactions across shared octahedral faces. The refined Cr3+ magnetic moments are typical of values seen in other oxides, suggesting that overlap of Cr 3d orbitals is not sufficient to form metal-metal bonds that lead to molecular orbitals that span the Cr2O9 bioctahedron.
PMID:
40632931
Bibliographic data and abstract were imported from PubMed on 10 Jul 2025.
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