Published April 11, 2012 | Version v1
Journal article

High-pressure phase transition of Bi2Fe4O9

  • 1. Institut für Geowissenschaften, Abteilung Kristallographie, Goethe-Universität Frankfurt, Altenhöferallee 1, D-60438 Frankfurt am Main (Germany)
  • 2. ESRF, BP 220, F-38043 Grenoble Cedex (France)
  • 3. DESY/HASYLAB, D-22603 Hamburg (Germany)
  • 4. Institut für Kristallographie, Universität zu Köln, D-50674 Cologne (Germany)

Description

The high-pressure behaviour of Bi2Fe4O9 was analysed by in situ powder and single-crystal x-ray diffraction and Raman spectroscopy. Pressures up to 34.3(8) GPa were generated using the diamond anvil cell technique. A reversible phase transition is observed at approximately 6.89(6) GPa and the high-pressure structure is stable up to 26.3(1) GPa. At higher pressures the onset of amorphization is observed. The crystal structures were refined from single-crystal data at ambient pressure and pressures of 4.49(2), 6.46(2), 7.26(2) and 9.4(1) GPa. The high-pressure structure is isotypic to the high-pressure structure of Bi2Ga4O9. The lower phase transition pressure of Bi2Fe4O9 with respect to that of Bi2Ga4O9 (16 GPa) confirms the previously proposed strong influence of cation substitution on the high-pressure stability and the misfit of Ga3+ and Fe3+ in tetrahedral coordination at high pressure. A fit of a second-order Birch-Murnaghan equation of state to the p-V data results in K0 = 74(3) GPa for the low-pressure phase and K0 = 79(2) GPa for the high-pressure phase. The mode Grüneisen parameters were obtained from Raman-spectroscopic measurements. (paper)

Availability note (English)

Available from http://dx.doi.org/10.1088/0953-8984/24/14/145401

Additional details

Publishing Information

Journal Title
Journal of Physics. Condensed Matter
Journal Volume
24
Journal Issue
14
Journal Page Range
[15 p.]
ISSN
0953-8984
CODEN
JCOMEL