Using a diamond anvil cell device and synchrotron radiation,the in-situ high-pressure structure of CaMnO3 has been investigated.In the pressure up to 36.5 GPa,no pressure-induced phase transition is observed.The pressure dependence on the lattice parameters of CaMnO3 is reported,and the relationship of the axial compression coefficients is βa 〉 βc 〉 βb.The isothermal bulk modulus K298=224(25) GPa is also obtained by fitting the pressure-volume data using the Murnaghan equation of state.
Using a diamond anvil cell device and synchrotron radiation, the in-situ high-pressure structure of SrMnO 3 has been investigated. At pressure up to 28.6 GPa, no pressure-induced phase transition is observed. The lattice parameters as a function of pressure is reported, and the relationship of the axial compression coefficients is β a 〉 β c . The isothermal bulk modulus K 298 =266(4) GPa is also obtained by fitting the pressure- volume data using the Murnaghan equation of state.
The structural stability of manganese titanate MnTiO3 at high pressure was investigated by X-ray diffraction and Raman spectroscopy with diamond anvil cells. Ilmenite-type MnTiO3 is stable at least to 26.6 GPa, and lithium niobate type MnTiO3 reversibly transforms at room temperature to perovskite at 2.0 GPa. Bulk moduli (K300) of ilmenite, lithium niobate and perovskite are 174(4) GPa, 179 (8) GPa, and 208(5) GPa, respectively (at fixed first pressure derivative K' = 4). The Griineisen parameter T has been estimated to be 1.28 for ilmenite and 1.75 for perovskite. In ilmenite phase, TiO6 octahedra become more regular with increasing pressure. In perovskite phase structural distortion increases with pressure increase.