Solid-state batteries with inorganic solid electrolytes are currently being discussed as a more reliable and safer future alternative to the current lithium-ion battery technology. To compete with state-of-theart lithium-ion batteries, solid electrolytes with higher ionic conductivities are needed, especially if thick electrode configurations are to be used. In the search for optimized ionic conductors, the lithium argyrodites have attracted a lot of interest. Here, we systematically explore the influence of aliovalent substitution in Li 6+x P 1−x Ge x S 5 I using a combination of X-ray and neutron diffraction, as well as impedance spectroscopy and nuclear magnetic resonance. With increasing Ge content, an anion site disorder is induced and the activation barrier for ionic motion drops significantly, leading to the fastest lithium argyrodite so far with 5.4 ± 0.8 mS cm −1 in a cold-pressed state and 18.4 ± 2.7 mS cm −1 upon sintering. These high ionic conductivities allow for successful implementation within a thick-electrode solid-state battery that shows negligible capacity fade over 150 cycles. The observed changes in the activation barrier and changing site disorder provide an additional approach toward designing better performing solid electrolytes.

We review case studies of diffusion in nanocrystalline ceramics, i.e. polycrystalline non-metallic materials with average grain sizes typically in the range from 5 to 50 nm. The experimental methods applied are, on the one hand, tracer diffusion or conductivity methods which are sensitive to macroscopic transport, and, on the other hand, NMR techniques which, complementarily to the previous ones, give access to microscopic diffusion parameters like atomic hopping rates and jump barrier heights. In all cases the diffusion properties of the samples, whether single-phase systems or composites, are dominated by their grain boundaries and interfacial regions, respectively. In principle, all experimental techniques allow one to discriminate between contributions to the diffusion from the crystalline grains and those from the interfacial regions. Corresponding examples are presented for SIMS and impedance measurements on oxygen conductors. NMR studies for various nanocrystalline lithium ion conductors reveal that two lithium species with different diffusivities are present. Comparison with the coarse grained counterparts shows that the slower ions are located inside the crystallites and the faster ones in the structurally disordered interfacial regions. Investigations on composite materials exhibit phenomena which can be explained by the percolation of fast diffusion pathways being formed by the interfaces between the two components.

The local structure phase diagram of (Li2S)x(P2S5)100−x thiophosphates derived from pair distribution function crystallization experiments.