Mixed-cation effect in a superprotonic phase of [(NH4)1 - xRbx]3H(SO4)2 studied by H solid-state NMR

• Published in: Solid state ionics 2008-07, Vol.179 (17-18), p.599-604
• Main Authors: Omi, Hironori, Suzuki, Koh-ichi, Hayashi, Shigenobu
• Format: Article
• Language: English
• ISSN: 0167-2738
• DOI: 10.1016/j.ssi.2008.04.021

Phase transitions and proton dynamics in [(NH4)1 - xRbx]3H(SO4)2 (0 < x < 1) have been studied by means of differential scanning calorimetry (DSC), thermogravimetric and differential thermal analyses (TG-DTA) and 1H solid-state NMR. Thermal analyses demonstrate that a phase transition from a room-temperature phase (phase II) to a high-temperature phase (phase I) takes place. The transition temperature increases with x. On the other hand, the melting/decomposition temperature is almost independent of x. Thus, the temperature range of phase I become narrower with x. The 1H MAS NMR spectra at room temperature demonstrate that the acidic protons form the stronger hydrogen bond with increase in x. This trend might correlate with the transition from phases II to I. 1H static NMR spectra indicate that the proton motions in [(NH4)1 - xRbx]3H(SO4)2 (0 < x < 1) are similar to those in (NH4)3H(SO4)2 and Rb3H(SO4)2, although the temperature ranges are different. In phase I, both NH4+ ions and the acidic protons diffuse translationally, which supports that phase I is superprotonic.