Nanosized helical magnetic domains in strongly frustrated
Abstract
Fe3PO4O3 forms a noncentrosymmetric lattice structure (space group R3m) comprising triangular motifs of Fe3+ coupled by strong antiferromagnetic interactions ( | ΘCW | > 900 K). Neutron diffraction from polycrystalline samples shows that strong frustration eventually gives way to an ordered helical incommensurate structure below TN =163 K, with the helical axis in the hexagonal ab plane and a modulation length to ~86 Å. The magnetic structure consists of an unusual needlelike correlation volume that extends past 900 Å along the hexagonal c axis but is limited to ~70 Å in the a b plane, despite the three-dimensional nature of the magnetic sublattice topology. The small in-plane correlation length, which persists to at least T = TN/40 , indicates a robust blocking of long-range order of the helical magnetic structure, and therefore stable domain walls, or other defect spin textures, must be abundant in Fe3PO4O3. Temperature-dependent neutron powder diffraction reveals small negative thermal expansion below TN. No change in lattice symmetry is observed on cooling through TN, as revealed by high-resolution synchrotron x-ray diffraction. The previously reported reduced moment of the Fe3+ ions (S = 5/2), μ ~ 4.2 μB, is confirmed here through magnetization studies of a magnetically dilutedmore »
- Authors:
-
- Colorado State Univ., Fort Collins, CO (United States)
- Publication Date:
- Research Org.:
- Argonne National Laboratory (ANL), Argonne, IL (United States)
- Sponsoring Org.:
- USDOE Office of Science (SC), Basic Energy Sciences (BES)
- OSTI Identifier:
- 1322370
- Alternate Identifier(s):
- OSTI ID: 1224362
- Resource Type:
- Accepted Manuscript
- Journal Name:
- Physical Review. B, Condensed Matter and Materials Physics
- Additional Journal Information:
- Journal Volume: 92; Journal Issue: 13; Journal ID: ISSN 1098-0121
- Publisher:
- American Physical Society (APS)
- Country of Publication:
- United States
- Language:
- ENGLISH
- Subject:
- 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
Citation Formats
Ross, K. A., Bordelon, M. M., Terho, G., and Neilson, J. R. Nanosized helical magnetic domains in strongly frustrated Fe3PO4O3. United States: N. p., 2015.
Web. doi:10.1103/PhysRevB.92.134419.
Ross, K. A., Bordelon, M. M., Terho, G., & Neilson, J. R. Nanosized helical magnetic domains in strongly frustrated Fe3PO4O3. United States. https://doi.org/10.1103/PhysRevB.92.134419
Ross, K. A., Bordelon, M. M., Terho, G., and Neilson, J. R. Mon .
"Nanosized helical magnetic domains in strongly frustrated Fe3PO4O3". United States. https://doi.org/10.1103/PhysRevB.92.134419. https://www.osti.gov/servlets/purl/1322370.
@article{osti_1322370,
title = {Nanosized helical magnetic domains in strongly frustrated Fe3PO4O3},
author = {Ross, K. A. and Bordelon, M. M. and Terho, G. and Neilson, J. R.},
abstractNote = {Fe3PO4O3 forms a noncentrosymmetric lattice structure (space group R3m) comprising triangular motifs of Fe3+ coupled by strong antiferromagnetic interactions ( | ΘCW | > 900 K). Neutron diffraction from polycrystalline samples shows that strong frustration eventually gives way to an ordered helical incommensurate structure below TN =163 K, with the helical axis in the hexagonal ab plane and a modulation length to ~86 Å. The magnetic structure consists of an unusual needlelike correlation volume that extends past 900 Å along the hexagonal c axis but is limited to ~70 Å in the a b plane, despite the three-dimensional nature of the magnetic sublattice topology. The small in-plane correlation length, which persists to at least T = TN/40 , indicates a robust blocking of long-range order of the helical magnetic structure, and therefore stable domain walls, or other defect spin textures, must be abundant in Fe3PO4O3. Temperature-dependent neutron powder diffraction reveals small negative thermal expansion below TN. No change in lattice symmetry is observed on cooling through TN, as revealed by high-resolution synchrotron x-ray diffraction. The previously reported reduced moment of the Fe3+ ions (S = 5/2), μ ~ 4.2 μB, is confirmed here through magnetization studies of a magnetically diluted solid solution series of compounds, Fe(3–x)GaxPO4O3, and is consistent with the refined magnetic moment from neutron diffraction 4.14(2) μB. Here, we attribute the reduced moment to a modified spin density distribution arising from ligand charge transfer in this insulating oxide.},
doi = {10.1103/PhysRevB.92.134419},
journal = {Physical Review. B, Condensed Matter and Materials Physics},
number = 13,
volume = 92,
place = {United States},
year = {Mon Oct 26 00:00:00 EDT 2015},
month = {Mon Oct 26 00:00:00 EDT 2015}
}
Web of Science
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