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Controlling inversion disorder in a stoichiometric spinel magnet.

ABSTRACT: In the study of frustrated quantum magnets, it is essential to be able to control the nature and degree of site disorder during the growth process, as many measurement techniques are incapable of distinguishing between site disorder and frustration-induced spin disorder. Pyrochlore-structured spinel oxides can serve as model systems of geometrically frustrated three-dimensional quantum magnets; however, the nature of the magnetism in one well-studied spinel, ZnFe₂O₄, remains unclear. Here, we demonstrate simultaneous control of both stoichiometry and inversion disorder in the growth of ZnFe₂O₄ single crystals, directly yielding a revised understanding of both the collective spin behavior and lattice symmetry. Crystals grown in the stoichiometric limit with minimal site inversion disorder contravene all the previously suggested exotic spin phases in ZnFe₂O₄. Furthermore, the structure is confirmed on the [Formula: see text] space group with broken inversion symmetry that induces antiferroelectricity. The effective tuning of magnetic behavior by site disorder in the presence of robust antiferroelectricity makes ZnFe₂O₄ of special interest to multiferroic devices.

SUBMITTER: Dronova MG

PROVIDER: S-EPMC9618041 | biostudies-literature | 2022 Oct

REPOSITORIES: biostudies-literature

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Controlling inversion disorder in a stoichiometric spinel magnet.

Dronova Margarita G MG Ye Feng F Cooper Scott E SE Krishnadas Anjana A Hoffmann Christina M CM Fujisawa Yuita Y Okada Yoshinori Y Khomskii Daniel I DI Feng Yejun Y

Proceedings of the National Academy of Sciences of the United States of America 20221018 43

In the study of frustrated quantum magnets, it is essential to be able to control the nature and degree of site disorder during the growth process, as many measurement techniques are incapable of distinguishing between site disorder and frustration-induced spin disorder. Pyrochlore-structured spinel oxides can serve as model systems of geometrically frustrated three-dimensional quantum magnets; however, the nature of the magnetism in one well-studied spinel, ZnFe<sub>2</sub>O<sub>4</sub>, remain ...[more]

PMID: 36256823

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Project description:Spinel iron oxide nanoparticles of different mean sizes in the range 10-25 nm have been prepared by surfactant-free up-scalable near- and super-critical hydro-thermal synthesis pathways and characterized using a wide range of advanced structural characterization methods to provide a highly detailed structural description. The atomic structure is examined by combined Rietveld analysis of synchrotron powder X-ray diffraction (PXRD) data and time-of-flight neutron powder-diffraction (NPD) data. The local atomic ordering is further analysed by pair distribution function (PDF) analysis of both X-ray and neutron total-scattering data. It is observed that a non-stoichiometric structural model based on a tetragonal γ-Fe2O3 phase with vacancy ordering in the structure (space group P43212) yields the best fit to the PXRD and total-scattering data. Detailed peak-profile analysis reveals a shorter coherence length for the superstructure, which may be attributed to the vacancy-ordered domains being smaller than the size of the crystallites and/or the presence of anti-phase boundaries, faulting or other disorder effects. The intermediate stoichiometry between that of γ-Fe2O3 and Fe3O4 is confirmed by refinement of the Fe/O stoichiometry in the scattering data and quantitative analysis of Mössbauer spectra. The structural characterization is complemented by nano/micro-structural analysis using transmission electron microscopy (TEM), elemental mapping using scanning TEM, energy-dispersive X-ray spectroscopy and the measurement of macroscopic magnetic properties using vibrating sample magnetometry. Notably, no evidence is found of a Fe3O4/γ-Fe2O3 core-shell nanostructure being present, which had previously been suggested for non-stoichiometric spinel iron oxide nanoparticles. Finally, the study is concluded using the magnetic PDF (mPDF) method to model the neutron total-scattering data and determine the local magnetic ordering and magnetic domain sizes in the iron oxide nanoparticles. The mPDF data analysis reveals ferrimagnetic collinear ordering of the spins in the structure and the magnetic domain sizes to be ∼60-70% of the total nanoparticle sizes. The present study is the first in which mPDF analysis has been applied to magnetic nanoparticles, establishing a successful precedent for future studies of magnetic nanoparticles using this technique.

Project description:The MgAl2O4-spinel has wide applications in various industries and in geosciences. It shows a significant inter-site Mg-Al cation exchange (denoted by the inversion parameter x), which modifies structural features, such as the unit-cell parameters and the sizes of the component polyhedra, and influences the physical and chemical properties. Previous studies mainly focused on the kinetics and thermodynamics of the Mg-Al exchange reaction, with the aim to ascertain the correlation between the inversion parameter and temperature; these studies, however, reached conflicting results. Here, we first reviewed the kinetics studies on the Mg-Al cation exchange reaction, and then reviewed all thermodynamic experiments, with special attention paid to the Mg-Al cation exchange equilibrium and the quench process, which might have modified the cation distributions once attained at high temperatures. We also assessed the accuracies in the temperature measurements and in the quantifications of the x by different analytical methods. With some necessary temperature correction and data removal, we have landed with a generally reliable x-T dataset covering the T-x space of 873 < T < 1887 K and 0.18(1) < x < 0.357(60) (71 data pairs in total). Fitting these x-T data to three most commonly used thermodynamic models, we have obtained more accurate model parameters. Further, we also evaluated the constituent items of the Gibbs free energy for the Mg-Al cation exchange reaction with experimental results from different research fields and reached the conclusion that highly possibly the T Δ S D should not be neglected. Based on this review, we suggest that: (1) Further kinetics study on the Mg-Al exchange reaction should be performed at both low T (<~973 K) and high T (>~1173 K); (2) further Mg-Al exchange equilibrium studies should be carried out at relatively low T and ambient P, as well as in vast ranges of simultaneous high P and high T; and (3) direct experimental measures about the entropies or the enthalpies of the MgAl2O4-spinels disordered to different extents should be conducted with full characterization of the starting materials and detailed description of the experimental procedures.

Dataset Information

Controlling inversion disorder in a stoichiometric spinel magnet.

Publications

Controlling inversion disorder in a stoichiometric spinel magnet.

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