J. Appl. Cryst. (2001). 34, 7-12 [ doi:10.1107/S0021889800013856 ]
Abstract: High-pressure synchrotron X-ray powder diffraction studies of TiP2O7, ZrP2O7 and ZrV2O7 have been performed. The ZrV2O7 structure undergoes a reversible transition at 1.38-1.58 GPa from cubic
- to pseudo-tetragonal
-ZrV2O7 that displays an orthorhombic 2 × 3 × 3 supercell. At pressures above 4 GPa, ZrV2O7 becomes irreversibly X-ray amorphous. No such transformations are observed for TiP2O7 and ZrP2O7, which compress smoothly up to the highest investigated pressures (40.3 and 20.5 GPa, respectively). These differences in high-pressure properties are discussed in terms of the negative thermal expansion of ZrV2O7. The bulk moduli at ambient pressure (B0) for TiP2O7, ZrP2O7,
-ZrV2O7 and
-ZrV2O7 were estimated to be 42 (3), 39 (1), 17.0 (7) and 20.8 (10) GPa, respectively.
Keywords: phase transformations; high-pressure diffraction; titanium pyrophosphate; zirconium pyrophosphate; zirconium pyrovanadate; negative thermal expansion; pressure amorphization.
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