Amorphization and decomposition of scandium molybdate at high pressure

The behavior of negative thermal-expansion material scandium molybdate Sc2(MoO4)3 is investigated at high pressure (HP) and high temperature (HT) using x-ray diffraction, Raman spectroscopy, and scanning electron microscopy. The compound exhibits unusually high compressibility (bulk modulus ~6 GPa) and undergoes amorphization at 12 GPa. On the other hand, in situ laser heating of amorphous samples inside the diamond-anvil cell is found to result in crystalline diffraction pattern and Raman spectrum different from those of the original compound. Upon release of the pressure subsequent to laser heating, the Raman spectrum and the diffraction pattern remain unchanged. Matching of several of the diffraction lines and Raman peaks in the laser-heated samples with those of MoO3 suggests a solid-state decomposition of the parent compound under HP-HT conditions into MoO3 and other compounds. Other diffraction lines are found to correspond to Sc2Mo2O9, Sc2O3, and the parent compound. Quantitative analysis of the characteristic x-ray emission from different regions of the sample during scanning electron microscopic observations is used for obtaining the compositions of the daughter compounds. The stoichiometries of two main phases are found to be close to those of MoO3 and Sc2Mo2O9. These results support the model that the pressure-induced amorphization occurred in this system because a pressure-induced decomposition was kinetically constrained