English
 
Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Mn3O4 under High Pressure and Temperature: Thermal Stability, Polymorphism, and Elastic Properties

Authors

Darul,  Jolanta
External Organizations;

/persons/resource/lathe

Lathe,  Christian
CGS Centre for Geological Storage, Geoengineering Centres, GFZ Publication Database, Deutsches GeoForschungsZentrum;

Piszora,  Paweł
External Organizations;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Darul, J., Lathe, C., Piszora, P. (2013): Mn3O4 under High Pressure and Temperature: Thermal Stability, Polymorphism, and Elastic Properties. - Journal of Physical Chemistry C, 117, 23487-23494.
https://doi.org/10.1021/jp404852j


Cite as: https://gfzpublic.gfz.de/pubman/item/item_328208
Abstract
We report results of in situ synchrotron X-ray diffraction studies of hausmannite up to 7.2 GPa and 1273 K. The Mn3O4 tetragonal spinel is found to transform to a 9.6% denser polymorph of the CaMn2O4-type structure at 7.2 GPa and 673 K, under milder conditions than those of any transformations to postspinel phase described so far. Upon heating at high pressure, the Mn3O4 phase undergoes decomposition and finally disappears in favor of MnO at temperatures above 1073 K. A fit of the pressure dependence of the volume of tetragonal phase to the Birch–Murnaghan equation of state yields the bulk modulus, K0, of 132.6 ± 3.1 GPa if the first pressure derivative of the bulk modulus is fixed to 4, and K0, of 102 ± 10 GPa for K0′ refined to 18.1 ± 5.6. Nonlinear compression behavior is observed for both crystallographic axes, with the c axis being more compressible than the a axis. Axial ratios in CaMn2O4-type Mn3O4 with temperature are also estimated. Surprisingly, the lattice distortion of the marokite-like phase is not preserved upon releasing pressure and temperature to ambient conditions.