Magnetic structure of greigite (Fe3S4) probed by neutron powder diffraction and polarized neutron diffraction
Magnetic structure of greigite (Fe3S4) probed by neutron powder diffraction and polarized neutron diffraction
We have investigated greigite (Fe3S4) using a combination of neutron powder diffraction and polarized neutron diffraction to give the first unambiguous assignment of its magnetic structure. Our results confirm that greigite has a collinear ferrimagnetic structure with antiferromagnetic coupling between the tetrahedral (A) and octahedral (B) sites. Our analysis also indicates that greigite does not have a significant vacancy concentration or spin canting. High-resolution neutron powder diffraction results enable determination of sublattice magnetizations of the A and B sites. At room temperature, the average magnetic moments on the two sites are almost the same (?3.0 ? B), with a net magnetic moment of ?3.0 ? B per formula unit (fu). The magnetic moment of the B sites decreases slightly between 10 K and room temperature, while the A site moment is relatively stable as a function of temperature; this indicates that greigite is probably an R-type ferrimagnet. At 10 K, the average magnetic moments of the A and B sites are 3.0 ? B and 3.25 ? B, respectively. Neutron diffraction measurements, coupled with magnetic measurements, on our pure synthetic greigite samples indicate that the saturation magnetization of greigite is lower than that of magnetite (Fe3O4). It is proposed that the lower magnetic moment in greigite (saturation magnetization is ?59 A m2 kg?1) compared to magnetite is probably caused by an increased degree of covalency between iron and sulfur compared to oxygen ligands or by greater delocalization of the 3d electrons in greigite.
B07101
Chang, Liao
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Rainford, Brian D.
a57f1153-bbba-49a3-bffc-0d96087156a0
Stewart, J. Ross
3496e62c-79c6-4cb0-9c64-cded71ddbc12
Ritter, Clemens
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Roberts, Andrew P.
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Tang, Yan
c187bb9c-4a92-4492-8ebe-21c55cd47209
Chen, Qianwang
b6cc3296-8996-4147-9f0c-963f0e432b63
11 July 2009
Chang, Liao
83123f49-dd71-43a9-a0b1-d80777231b44
Rainford, Brian D.
a57f1153-bbba-49a3-bffc-0d96087156a0
Stewart, J. Ross
3496e62c-79c6-4cb0-9c64-cded71ddbc12
Ritter, Clemens
6de4abcd-30c0-410f-8ccc-a6b5a6a79d01
Roberts, Andrew P.
4f062491-5408-4edb-8dd1-140c6a42e93f
Tang, Yan
c187bb9c-4a92-4492-8ebe-21c55cd47209
Chen, Qianwang
b6cc3296-8996-4147-9f0c-963f0e432b63
Chang, Liao, Rainford, Brian D., Stewart, J. Ross, Ritter, Clemens, Roberts, Andrew P., Tang, Yan and Chen, Qianwang
(2009)
Magnetic structure of greigite (Fe3S4) probed by neutron powder diffraction and polarized neutron diffraction.
Journal of Geophysical Research, 114, .
(doi:10.1029/2008JB006260).
Abstract
We have investigated greigite (Fe3S4) using a combination of neutron powder diffraction and polarized neutron diffraction to give the first unambiguous assignment of its magnetic structure. Our results confirm that greigite has a collinear ferrimagnetic structure with antiferromagnetic coupling between the tetrahedral (A) and octahedral (B) sites. Our analysis also indicates that greigite does not have a significant vacancy concentration or spin canting. High-resolution neutron powder diffraction results enable determination of sublattice magnetizations of the A and B sites. At room temperature, the average magnetic moments on the two sites are almost the same (?3.0 ? B), with a net magnetic moment of ?3.0 ? B per formula unit (fu). The magnetic moment of the B sites decreases slightly between 10 K and room temperature, while the A site moment is relatively stable as a function of temperature; this indicates that greigite is probably an R-type ferrimagnet. At 10 K, the average magnetic moments of the A and B sites are 3.0 ? B and 3.25 ? B, respectively. Neutron diffraction measurements, coupled with magnetic measurements, on our pure synthetic greigite samples indicate that the saturation magnetization of greigite is lower than that of magnetite (Fe3O4). It is proposed that the lower magnetic moment in greigite (saturation magnetization is ?59 A m2 kg?1) compared to magnetite is probably caused by an increased degree of covalency between iron and sulfur compared to oxygen ligands or by greater delocalization of the 3d electrons in greigite.
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Submitted date: 17 December 2008
Published date: 11 July 2009
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Local EPrints ID: 68602
URI: http://eprints.soton.ac.uk/id/eprint/68602
ISSN: 0148-0227
PURE UUID: 4ae3adbf-02c8-49c9-8b48-a243822c5a8a
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Date deposited: 03 Sep 2009
Last modified: 13 Mar 2024 18:59
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Contributors
Author:
Liao Chang
Author:
Brian D. Rainford
Author:
J. Ross Stewart
Author:
Clemens Ritter
Author:
Andrew P. Roberts
Author:
Yan Tang
Author:
Qianwang Chen
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