Structural complexity of simple Fe2O3 at high pressures and temperatures
E. Bykova (),
L. Dubrovinsky,
N. Dubrovinskaia,
M. Bykov,
C. McCammon,
S. V. Ovsyannikov,
H. -P. Liermann,
I. Kupenko,
A. I. Chumakov,
R. Rüffer,
M. Hanfland and
V. Prakapenka
Additional contact information
E. Bykova: Bayerisches Geoinstitut, University of Bayreuth
L. Dubrovinsky: Bayerisches Geoinstitut, University of Bayreuth
N. Dubrovinskaia: Laboratory of Crystallography, University of Bayreuth
M. Bykov: Bayerisches Geoinstitut, University of Bayreuth
C. McCammon: Bayerisches Geoinstitut, University of Bayreuth
S. V. Ovsyannikov: Bayerisches Geoinstitut, University of Bayreuth
H. -P. Liermann: Photon Sciences, Deutsches Elektronen-Synchrotron
I. Kupenko: Bayerisches Geoinstitut, University of Bayreuth
A. I. Chumakov: European Synchrotron Radiation Facility
R. Rüffer: European Synchrotron Radiation Facility
M. Hanfland: European Synchrotron Radiation Facility
V. Prakapenka: Center for Advanced Radiation Sources, University of Chicago, 9700 South Cass Avenue, Illinois, Argonne 60437, USA
Nature Communications, 2016, vol. 7, issue 1, 1-6
Abstract:
Abstract Although chemically very simple, Fe2O3 is known to undergo a series of enigmatic structural, electronic and magnetic transformations at high pressures and high temperatures. So far, these transformations have neither been correctly described nor understood because of the lack of structural data. Here we report a systematic investigation of the behaviour of Fe2O3 at pressures over 100 GPa and temperatures above 2,500 K employing single crystal X-ray diffraction and synchrotron Mössbauer source spectroscopy. Crystal chemical analysis of structures presented here and known Fe(II, III) oxides shows their fundamental relationships and that they can be described by the homologous series nFeO·mFe2O3. Decomposition of Fe2O3 and Fe3O4 observed at pressures above 60 GPa and temperatures of 2,000 K leads to crystallization of unusual Fe5O7 and Fe25O32 phases with release of oxygen. Our findings suggest that mixed-valence iron oxides may play a significant role in oxygen cycling between earth reservoirs.
Date: 2016
References: Add references at CitEc
Citations:
Downloads: (external link)
https://www.nature.com/articles/ncomms10661 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10661
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/ncomms10661
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().