A Raman spectroscopic study of the phase transition of BaZr(PO4)2: Evidence for a trigonal structure of the high-temperature polymorph

We have studied the structural evolution of monoclinic BaZr(PO4)2 during heating up to 835 K by Raman spectroscopy. In agreement with previous studies we found a first-order phase transition at about 730 K during heating while upon cooling the reverse transition occurs at 705 K. However, some disagreement about the crystal structure of the high-temperature polymorph occurs in the literature. While the space group has not yet been determined, the X-ray diffraction pattern of the high-temperature phase has been indexed on either an orthorhombic or a hexagonal unit cell. We found that the number of Raman active internal PO4 vibrational modes decrease from nine to six during the transition. A group theoretical survey through all orthorhombic, trigonal, and hexagonal factor groups revealed that the observed number of vibrations would only be consistent with the Ba and Zr atoms located at a D3d(3¯m) site, the P and two O atoms at a C3v(3m), and six O atoms at a Cs(m) site in the D3d   factor group. Based on our Raman data, the space group of the high-temperature polymorph is thus either D3d1(P3¯1m), D3d3(P3¯m1), or D3d5(R3¯m).

Raman mode frequencies of the PO4 stretching vibrations in BaZr(PO4)2 as a function of temperature during heating and cooling across the phase transition temperature near 730 K.Figure optionsDownload as PowerPoint slide