We present a detailed study on the exact location and dynamics of Li ions in the garnet-type material Li(5)La(3)Nb(2)O(12) employing advanced solid state NMR strategies. Applying temperature-dependent (7)Li-NMR, (6)Li-MAS-NMR, (6)Li-{(7)Li}-CPMAS-NMR, (6)Li-{(7)Li}-CPMAS-REDOR-NMR as well as 2D-(6)Li-{(7)Li}-CPMAS-Exchange-NMR spectroscopy, we were able to quantify the distribution of the Li cations among the various possible sites within the garnet-type structure and to identify intrinsic details of Li migration. The results indicate a sensitive dependence of the distribution of Li cations among the tetrahedral and octahedral sites on the temperature of the final annealing process. This distribution profoundly affects the mobility of the Li cations within the garnet-type framework structure. Extended Li mobility at ambient temperature is only possible if the majority of the Li cations is accommodated in the octahedral sites, as observed for the sample annealed at 900 degrees C. Octahedrally-coordinated Li cations could be identified as the mobile Li species, whereas the tetrahedral sites seem to act as a trap for the Li cations, rendering the tetrahedrally-coordinated Li cations immobile on the time scale of the NMR experiments.

In this contribution, we report on a novel composite solid electrolyte material, SiO2/[BMIM]BF4/LiTf ([BMIM]BF4 = 1-butyl-3-methylimidazolium tetrafluoroborate, LiTf = lithium trifluoromethanesulfonate), prepared via a one-pot sol−gel synthesis route, in which the amorphous SiO2 glass network provides the mechanical stability and the ionic liquid/Li salt part the high ionic conductivity (0.5 × 10−2 S cm−1 at 298 K). The mobility of the ionic liquid and Li salt confined within the pores of the fully condensed SiO2 network is found to increase with the [BMIM]BF4/LiTf ratio, exhibiting an almost liquidlike mobility, as evidenced by multinuclear solid-state NMR, pulsed-field-gradient solid-state NMR, and impedance spectroscopy.

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Ionic TransportResearch on solid ionic conductors for use as electrolytes in all solid state batteries still constitutes a rather vivid branch of today's materials science. Despite enormous efforts, neither the development of a solid electrolyte fulfilling the key requirements such as mechanical stability and high ionic conductivity at ambient temperature has been successful nor has an extended understanding of the local Li coordination motifs in the often amorphous systems been obtained. In this contribution, recent progress both in the development of novel solid state electrolytes with high ionic conductivity and mechanical stability and in the characterization of the local Li coordination motifs in these electrolytes from our laboratory is presented. The work was performed as a project within the framework of the Collaborative Research Centre SFB 458 "Ionic Motion in Materials with Disordered Structures -From Elementary Steps to Macroscopic Transport". Results will be given for polymer electrolytes based on polyethylene oxide (PEO), polyphosphazene (PPZ) and polyacrylonitrile (PAN) with various Li salts, nano-composites of these polymer electrolytes and Al 2 O 3 as a ceramic filler, novel inorganic/organic hybrid electrolytes, in which a mixture of an ionic liquid and Li salt is confined within the pore system of a SiO 2 glass, and a crystalline electrolyte, Li 5 La 3 Nb 2 O 12 . Employing a range of advanced solid state NMR methodologies including dipolar based NMR techniques and pulsed field gradient (PFG) NMR and impedance spectroscopy we were able to obtain a detailed knowledge about the local Li cation coordination motifs and the mechanism of Li transport in these electrolytes. Especially the hybrid electrolytes and the salt rich PAN based polymer electrolytes were identified as rather promising materials which combine a high ionic conductivity and mechanical stability.

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