Dynamics of the α-β phase transitions in quartz and cristobalite as observed by in-situ high temperature 29Si and 17O NMR
Tóm tắt
Relaxation times (T1) and lineshapes were examined as a function of temperature through the α-β transition for 29Si in a single crystal of amethyst, and for 29Si and 17O in cristobalite powders. For single crystal quartz, the three 29Si peaks observed at room temperature, representing each of the three differently oriented SiO4 tetrahedra in the unit cell, coalesce with increasing temperature such that at the α-β transition only one peak is observed. 29Si T1's decrease with increasing temperature up to the transition, above which they remain constant. Although these results are not uniquely interpretable, hopping between the Dauphiné twin related configurations, α1 and α2, may be the fluctuations responsible for both effects. This exchange becomes observable up to 150° C below the transition, and persists above the transition, resulting in β-quartz being a time and space average of α1 and α2. 29Si T1's for isotopically enriched powdered cristobalite show much the same behavior as observed for quartz. In addition, 17O T1's decrease slowly up to the α-β transition at which point there is an abrupt 1.5 order of magnitude drop. Fitting of static powder 17O spectra for cristobalite gives an asymmetry parameter (η) of 0.125 at room T, which decreases to <0.040 at the transition temperature. The electric field gradient (EFG) and chemical shift anisotropy (CSA), however, remain the same, suggesting that the decrease in η is caused by a dynamical rotation of the tetrahedra below the transition. Thus, the mechanisms of the α-β phase transitions in quartz and cristobalite are similar: there appears to be some fluctuation of the tetrahedra between twin-related orientations below the transition temperature, and the β-phase is characterized by a dynamical average of the twin domains on a unit cell scale.
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