VIBRATIONAL-MODES AND STRUCTURE OF RARE-EARTH-HALIDE ALKALI-HALIDE BINARY MELTS - YBR3-ABR (A=LI, K, CS) AND YF3-KF

Citation
V. Dracopoulos et al., VIBRATIONAL-MODES AND STRUCTURE OF RARE-EARTH-HALIDE ALKALI-HALIDE BINARY MELTS - YBR3-ABR (A=LI, K, CS) AND YF3-KF, Journal of the Chemical Society. Faraday transactions, 93(17), 1997, pp. 3081-3088
Citations number
32
Categorie Soggetti
Chemistry Physical","Physics, Atomic, Molecular & Chemical
ISSN journal
09565000
Volume
93
Issue
17
Year of publication
1997
Pages
3081 - 3088
Database
ISI
SICI code
0956-5000(1997)93:17<3081:VASORA>2.0.ZU;2-6
Abstract
Raman spectra of the following binary molten salt systems have been me asured: (a) YBr3-ABr (A = Li, K, Cs) at temperatures up to 920 degrees C and at different compositions; (b) YF3-KF at temperatures up to 100 0 degrees C and compositions up to 50% YF3. The spectral changes occur ring upon melting of Cs2NaYBr6, YBr3 and K3YF6 crystalline compounds w ere also measured. The data indicate that, in mixtures rich in alkali halide, YX63-(X = F, Br) octahedra are the predominant species giving rise to two main bands P-1 (polarized) and D-1 (depolarized) which are assigned as follows: (a) YBr63-, P-1 = 156 cm(-1), v(1)(A(1g)) and D- 1 = 78 cm(-1), v(5) (F-2g); and (b) YF63-, P-1 = 445 cm(-1), v(1)(A(1g ) and D-1 = 225 cm(-1), v(5)(F-2g). In molten mixtures rich in YBr3 in addition to the P-1 and D-1 bands a new depolarized D-2 (ca. 210 cm(- 1)) and a strong new polarized P-2 band appear in the spectra. The P-2 band shifts from ca. 200 cm(-1) to ca. 250 cm(-1) with increasing YBr , content. The presence of these four bands and their polarization cha racteristics suggest that the predominant vibrational modes in the YBr 3-rich mixtures are due to a close C-3v pyramidal like 'unit' arising from the D-3 distortions of the YBr63- octahedra bound by edges in the melt. This behaviour, as well as the spectral changes upon melting YB r3, supports the view that the structure of pure molten YBr3 consists of edge-sharing distorted octahedra. The molten fluoride mixtures YF3- KF at composition X-YF3 > 0.25 also show four bands, two depolarized a t ca. 240 cm(-1) (D-1), ca. 370 cm(-1) (D-2) and two overlapping polar ized bands at ca. 440 cm(-1) (P-1), ca. 460 cm(-1) (P-2). Finally, the trends of the YX3-KX spectra on going from the bromide to chloride to fluoride melts suggest that pure molten YF3 is likely to possess a lo ose 'network' structure of edge-bridged distorted octahedra as in the case of molten YCl3 and YBr3.