Fast proton conducting hydrogen sulphates and selenates: Impedance spectroscopy, Raman scattering and optical microscope study

In the paper the phenomenon of proton conductivity in hydrogen bonded acidic sulphate and selenate salts of alkali metals is discussed. The superionic proton conducting state in the crystals is achieved as a result of structural phase transition at T-s. The specific features of H-bond make it easily adaptable to its environment, hence the fast proton transport is assisted by dynamics of neighbouring species. In the crystals there appear additional, symmetry equivalent positions for protons above T-s, so the occupancy of H-bonds c < 1. This results in formation of a dynamically disordered H-bond network, which enables significant proton conductivity by Grotthuss mechanism. In most of M3H(XO4)(2)-type crystals T-s coincides with ferroelastic-paraelastic phase transition temperature T-c. All the ferroelastic compounds exhibit an intermediate phase close to Ts, where anomalies of physical properties are observed. The experimental data indicate, that intensive ferroelastic twinning assists transformation of H-bond network from ordered to disordered state. Therefore smooth and reversible superionic phase transition is observed in the ferroelastic crystals. On the other hand, non-ferroelastic Rb3H(SO4)(2) crystal, whose structure cannot be transformed gradually, undergoes an irreversible reconstructive transformation into a polycrystalline state at T-s. (c) 2005 Elsevier B.V. All rights reserved.