RESUMEN
Modifying lithium niobate cation composition improves not only the functional properties of the acousto- and optoelectronic materials as well as ferroelectrics but elevates the protonic transfer in LiNbO3-based electrolytes of the solid oxide electrochemical devices. Molten chlorides and other thermally stable salts are not considered practically as the precursors to synthesize and modify oxide compounds. This article presents and discusses the results of an experimental study of the full or partial heterovalent substitution of lithium ion in nanosized LiNbO3 powders and in the surface layer of LiNbO3 single crystal using molten salt mixtures containing calcium, lead, and rare-earth metals (REM) chlorides as the precursors. The special features of heterovalent ion exchange in chloride melts are revealed such as hetero-epitaxial cation exchange at the interface PbCl2-containing melt/lithium niobate single crystal; the formation of Li(1−x) Ca(x/2)V(x/2)Li+ NbO3 solid solutions with cation vacancies as an intermediate product of the reaction of heterovalent substitution of lithium ion by calcium in LiNbO3 powders; the formation of lanthanide orthoniobates with a tetragonal crystal structure such as scheelite as the result of lithium niobate interaction with trichlorides of rare-earth elements. It is shown that the fundamental properties of ion-modifiers (ion radius, nominal charge), temperature, and duration of isothermal treatment determine the products' chemical composition and the rate of heterovalent substitution of Li+-ion in lithium niobate.
RESUMEN
Li6-xZr2-xAxO7 (A = Nb; Ta) system with 0 < x < 0.30 is synthesized by glycine-nitrate method. Boundaries of solid solutions based on monoclinic Li6Zr2O7 are determined; temperature (200-600 °C) and concentration dependences of conductivity are investigated. It is shown that monoclinic Li6Zr2O7 exhibits better transport properties compared to its triclinic modification. Li5.8Zr1.8Nb(Ta)0.2O7 solid solutions have a higher lithium-cation conductivity at 300 °C compared to solid electrolytes based on other lithium zirconates due the "open" structure of monoclinic Li6Zr2O7 and a high solubility of the doping cations.