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Free keywords:
Aluminum; Cesium; Polymorphism; NMR spectroscopy; Solid-state structures
Abstract:
A new tetragonal phase of CsAlH4 was observed after the precipitation of CsAlH4 from a diglyme solution with an inert solvent. This new phase and the previously described orthorhombic phase were characterized by a combination of X-ray powder diffraction analysis and 27Al and 133Cs solid-state NMR spectroscopy. The transformation of the tetragonal CsAlH4 phase into the orthorhombic CsAlH4 phase can be induced by thermal treatment, whereas the opposite process can be stimulated by mechanical treatment. The phase transformation processes are almost completely reversible and can be performed several times without any observable decomposition of CsAlH4. The structure of the tetragonal CCsAlH4 phase (space group I41/a) was solved from X-ray powder diffraction data, and the lattice parameters were determined to be a = 5.6732(4) and c = 14.2795(11) Å.
