Antiferromagnetism,Anion Disorder, and Lattice Defectsin the <i>S</i> = 5/2 [Bi<sub>2</sub>O<sub>2</sub>][Mn<sup>2+</sup>F<sub>4</sub>] Aurivillius Compound

[Bi<sub>2</sub>O<sub>2</sub>][MnF<sub>4</sub>] is an Aurivillius oxyfluoride phase with Mn<sup>2+</sup> cations filling the one-layer perovskite subunits. Its synthesis as a single-phase material by a high-temperature solid-state route is complicated by the high volatility of fluorine in the used precursors and by its limited thermal stability above 400 °C. Its crystal structure was determined using synchrotron and neutron diffraction data. It shows structural singularities, highlighted by the anion positional disorder inherent to the <i>I</i>4/<i>mmm</i> space group, despite the evidence of strong local axial and equatorial octahedral tilts along with clues for ideal F<sup>–</sup> and O<sup>2–</sup> total segregation in the two-layered subunits. Contrarily to the M = Ni<sup>2+</sup>, Co<sup>2+</sup>, and Fe<sup>2+/3+</sup> analogs, where similar tilts order in various supercells, for M = Mn<sup>2+</sup> only short-range ordering (SRO) was detected by electron diffraction. This was rationalized in terms of the d<sup>5</sup> ion isotropic nature for which weak distortions of the crystal field do not have an energy penalty and favor local octahedral defects acting as antiphase boundaries between nanometric SRO domains. DFT calculations validate equiprobable tilted [MnF<sub>6</sub>] arrangements in the perovskite layers and suggest the possibility for an O ↔ F exchange between the [Bi<sub>2</sub>O<sub>2</sub>] and [MnF<sub>4</sub>] modules, supported by HAADF imaging. The presence of oxygen and vacancies in the perovskite slabs was also detected in samples prepared at higher temperatures. [Bi<sub>2</sub>O<sub>2</sub>][MnF<sub>4</sub>] magnetic structure shows a colinear antiferromagnetic arrangement below <i>T</i><sub>N</sub> = 19.8 K, with Mn<sup>2+</sup> spins (<i>S</i> = 5/2, <i>L</i> = 0) aligned parallel to the <i>c</i>-axis (<i>M</i><sub><i>z</i></sub> = 3.8(2) μ<sub>B</sub>/Mn). This is again in contrast with the systematic spin-canting responsible for weak ferromagnetism in the previous M<sup>2+</sup> Aurivillius compounds. Finally, the modest fluoride ionic mobility was measured in a small temperature range, restricted by the stability of the compound in air.

Publication Details

Journal
Figshare
Published
2025-07-23
DOI
https://doi.org/10.1021/acs.chemmater.5c01072.s001
Primary Topic
Inorganic Fluorides and Related Compounds
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Antiferromagnetism,Anion Disorder, and Lattice Defectsin the S = 5/2 [Bi2O2][Mn2+F4] Aurivillius Compound

Figshare
Inorganic Fluorides and Related Compounds
article

Antiferromagnetism,Anion Disorder, and Lattice Defectsin the S = 5/2 [Bi2O2][Mn2+F4] Aurivillius Compound

article en

Abstract

[Bi<sub>2</sub>O<sub>2</sub>][MnF<sub>4</sub>] is an Aurivillius oxyfluoride phase with Mn<sup>2+</sup> cations filling the one-layer perovskite subunits. Its synthesis as a single-phase material by a high-temperature solid-state route is complicated by the high volatility of fluorine in the used precursors and by its limited thermal stability above 400 °C. Its crystal structure was determined using synchrotron and neutron diffraction data. It shows structural singularities, highlighted by the anion positional disorder inherent to the <i>I</i>4/<i>mmm</i> space group, despite the evidence of strong local axial and equatorial octahedral tilts along with clues for ideal F<sup>–</sup> and O<sup>2–</sup> total segregation in the two-layered subunits. Contrarily to the M = Ni<sup>2+</sup>, Co<sup>2+</sup>, and Fe<sup>2+/3+</sup> analogs, where similar tilts order in various supercells, for M = Mn<sup>2+</sup> only short-range ordering (SRO) was detected by electron diffraction. This was rationalized in terms of the d<sup>5</sup> ion isotropic nature for which weak distortions of the crystal field do not have an energy penalty and favor local octahedral defects acting as antiphase boundaries between nanometric SRO domains. DFT calculations validate equiprobable tilted [MnF<sub>6</sub>] arrangements in the perovskite layers and suggest the possibility for an O ↔ F exchange between the [Bi<sub>2</sub>O<sub>2</sub>] and [MnF<sub>4</sub>] modules, supported by HAADF imaging. The presence of oxygen and vacancies in the perovskite slabs was also detected in samples prepared at higher temperatures. [Bi<sub>2</sub>O<sub>2</sub>][MnF<sub>4</sub>] magnetic structure shows a colinear antiferromagnetic arrangement below <i>T</i><sub>N</sub> = 19.8 K, with Mn<sup>2+</sup> spins (<i>S</i> = 5/2, <i>L</i> = 0) aligned parallel to the <i>c</i>-axis (<i>M</i><sub><i>z</i></sub> = 3.8(2) μ<sub>B</sub>/Mn). This is again in contrast with the systematic spin-canting responsible for weak ferromagnetism in the previous M<sup>2+</sup> Aurivillius compounds. Finally, the modest fluoride ionic mobility was measured in a small temperature range, restricted by the stability of the compound in air.

Figshare
Affordable and clean energy
Openalex Percentile: Top 61%
Inorganic Fluorides and Related Compounds
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Antiferromagnetism,Anion Disorder, and Lattice Defectsin the <i>S</i> = 5/2 [Bi<sub>2</sub>O<sub>2</sub>][Mn<sup>2+</sup>F<sub>4</sub>] Aurivillius Compound · Figshare (2025) | TGRS Research Map | TGRS