Effect of devitrification on ion motion in lithium-disilicate glass

Li-disilicate glass-ceramics consist of microcrystallites imbedded in the glassy Li2O · 2SiO2 matrix where the number and size of the crystallites depend on the devitrification heat treatment. To assess ion motion in these model glass-ceramics, we have measured the temperature dependence of the dc conductivity, σdc, and the 7Li nuclear spin relaxation (NSR) rate, 1/T1, in samples with various crystalline fraction, c, ranging from c = 0 (pure glass) to c = 1 (fully devitrified polycrystalline ceramic). The Cole–Cole presentation of the complex impedance shows two separate arcs caused by the remarkable difference of the ionic motion in the glassy and crystalline phase. These two arcs correspond to a bi-exponential decay of the 7Li nuclear spin magnetization where the resulting two NSR rates are induced by the ionic motion in the two phases. Thus the NSR and σdc data provide a comprehensive picture of the ionic motion in the glassy and crystalline phases. In particular, the ionic motion is the fastest in the glass; then at lower values of c we observe a metastable crystalline phase with ionic motion much greater than in the stable (LS2) crystalline phase existing at large c-values.