Temperature-dependent structural study of microporous CsAlSi5O12

CsAlSi5O12 crystals were synthesized at high temperature by slow cooling of a vanadium oxide flux. Single-crystal X-ray diffraction structure analysis and electron microprobe analyses yielded the microporous CAS zeolite framework structure of Cs0.85Al0.85Si5.15O12 composition. High-temperature single-crystal and powder X-ray diffraction studies were utilized to analyze anisotropic thermal expansion. Rietveld refined cell constants from powder diffraction data, measured in steps of 25 °C up to 700 °C, show a significant decrease in expansion above 500 °C. At 500 °C, a displacive, static disorder–dynamic disorder-type phase transition from the acentric low-temperature space group Ama2 to centrosymmetric Amam (Cmcm in standard setting) was found. Thermal expansion below the phase transition is governed by rigid-body TO4 rotations accompanied by stretching of T–O–T angles. Above the phase transition at 500 °C all atoms, except one oxygen (O6), are fixed on mirror planes. Temperature-dependent polarized Raman single-crystal spectra between −270 and 300 °C and unpolarized spectra between room temperature and 1000 °C become increasingly less resolved with rising temperature confirming the disordered static–disordered dynamic type of the phase transition.

Temperature-dependent structural evolution of microporous CsAlSi5O12 has been investigated by single-crystal and powder X-ray diffraction, as well as Raman spectroscopy. Results yielded a phase transition of order–disorder type.Figure optionsDownload as PowerPoint slide