Raman Spectrum of Gadolinium Molybdate Above and Below the Ferroelectric Transition

Authors

• Frank Ullman, University of Nebraska-Lincoln
• B. J. Holden, University of Nebraska-Lincoln
• B. N. Ganguly, Ganguly
• John R. Hardy, University of Nebraska-Lincoln

Document Type

Article

Date of this Version

9-15-1973

Citation

Physical Review (September 15, 1973) 8(6)

Comments

Copyright 1973, American Physical Society. Used by permission

Abstract

90 °-scattered Raman spectra of single-domain gadolinium molybdate have been obtained at room temperature and above the 159 °C ferroelectric transition on several crystal orientations. Lines in the 0-200-cm^-1 range can all be associated with Raman-active phonons and are identified by symmetry considerations, scattering-efficiency calculations, and comparison of spectra for different crystal orientations. Lines in the 200-1000-cm^-1 range can be identified with coupled vibrations of tetrahedral molybdate ions. Spectra for frequencies above 1,000 cm^-1 originate from impurity flourescence. The effect of the presence of multiple domains on the spectra was determined; the observed differences between single-domain and multiple-domain crystals result from B₁-B₂ symmetry mixing from the twinning of adjacent domains. No new soft modes, in addition to the known soft mode at about 43 cm^-1, were observed. A few of the lines that are present in only the low-temperature phase cannot be identified from symmetry analysis and are probably derived from zone-boundary modes of the high-temperature phase.