Sr<sub>4</sub>Os<sub>3</sub>O<sub>12</sub> – A Layered Osmate(V,VI) that is Magnetic Close to Room Temperature

Abstract Black crystals of the mixed‐valence osmate(V,VI) Sr 4 Os 3 O 12 were grown via a gas phase reaction in an evacuated silica tube. The material is attracted to a permanent magnet at room temperature (295±5 K) but loses this property when heated or cooled. In this temperature interval, soft magnetic behavior with vanishing coercivity is observed, but the saturation magnetization is only 0.05 μ B per formula unit. Resistivity measurements show that Sr 4 Os 3 O 12 is a semiconductor with a small band gap of about 0.26 eV at room temperature. X‐ray diffraction on a single‐crystal revealed a rhombohedral structure with the space group R m and lattice parameters a r =554.64(2) pm and c r =2700.1(1) pm at 300(1) K. The compound crystallizes in the La 4 Ti 3 O 12 structure type and is isostructural to Sr 4 CoRe 2 O 12 . The structure is a rhombohedral stack of layered blocks, each of which can be considered as a section of three layers of the cubic perovskite structure cut perpendicular to one of its threefold axes. The Os–O−Os bond angle of about 175° favors superexchange that leads to antiferromagnetic coupling between the osmium atoms with 5 d 3 and 5 d 2 configurations. Sr 4 Os 3 O 12 exhibits strong lattice dynamics. One aspect is the antiferro‐rotative lattice modes of the corner‐sharing [OsO 6 ] octahedra, which freeze upon cooling. At 100 K, an ordered, yet twinned triclinic superstructure is formed. Strong spin‐orbit coupling and other effects cause deformations of the [OsO 6 ] octahedra that differ significantly at 300 K and 100 K, suggesting a change in the electronic configuration. Competing ground states could also explain the temperature‐dependent band gap and the magnetic fluctuations manifested in the magnetization peak at room temperature.

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Journal
Zeitschrift für anorganische und allgemeine Chemie
Published
2024-08-20
DOI
https://doi.org/10.1002/zaac.202400109
Primary Topic
Advanced Condensed Matter Physics
Type
article
Field-Weighted Citation Impact
0.00

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article

Sr4Os3O12 – A Layered Osmate(V,VI) that is Magnetic Close to Room Temperature

Julia‐Maria Hübner, Gohil S. Thakur, Kati Finzel, Michael Ruck et al.
Zeitschrift für anorganische und allgemeine Chemie
Advanced Condensed Matter Physics
article

Sr4Os3O12 – A Layered Osmate(V,VI) that is Magnetic Close to Room Temperature

Julia‐Maria Hübner, Gohil S. Thakur, Kati Finzel, Michael Ruck, Thomas Doert
article en

Abstract

Abstract Black crystals of the mixed‐valence osmate(V,VI) Sr 4 Os 3 O 12 were grown via a gas phase reaction in an evacuated silica tube. The material is attracted to a permanent magnet at room temperature (295±5 K) but loses this property when heated or cooled. In this temperature interval, soft magnetic behavior with vanishing coercivity is observed, but the saturation magnetization is only 0.05 μ B per formula unit. Resistivity measurements show that Sr 4 Os 3 O 12 is a semiconductor with a small band gap of about 0.26 eV at room temperature. X‐ray diffraction on a single‐crystal revealed a rhombohedral structure with the space group R m and lattice parameters a r =554.64(2) pm and c r =2700.1(1) pm at 300(1) K. The compound crystallizes in the La 4 Ti 3 O 12 structure type and is isostructural to Sr 4 CoRe 2 O 12 . The structure is a rhombohedral stack of layered blocks, each of which can be considered as a section of three layers of the cubic perovskite structure cut perpendicular to one of its threefold axes. The Os–O−Os bond angle of about 175° favors superexchange that leads to antiferromagnetic coupling between the osmium atoms with 5 d 3 and 5 d 2 configurations. Sr 4 Os 3 O 12 exhibits strong lattice dynamics. One aspect is the antiferro‐rotative lattice modes of the corner‐sharing [OsO 6 ] octahedra, which freeze upon cooling. At 100 K, an ordered, yet twinned triclinic superstructure is formed. Strong spin‐orbit coupling and other effects cause deformations of the [OsO 6 ] octahedra that differ significantly at 300 K and 100 K, suggesting a change in the electronic configuration. Competing ground states could also explain the temperature‐dependent band gap and the magnetic fluctuations manifested in the magnetization peak at room temperature.

Zeitschrift für anorganische und allgemeine ChemieVol. 650(21)
Complexity, Topology and Dynamics in Quantum Matter (DE), Max Planck Institute for Chemical Physics of Solids (DE), Indian Institute of Science Education and Research Berhampur (IN), Technische Universität Dresden (DE)
Deutsche Forschungsgemeinschaft
Openalex Percentile: Top 92%
Advanced Condensed Matter Physics
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