<p>Driven by the increasing attention that the superionic conductors Li<sub>3</sub>MX<sub>6</sub> (M = Y, Er, In, La; X = Cl, Br, I) have gained recently for the use of solid-state batteries, and the idea that a softer, more polarizable anion sublattice is beneficial for ionic transport, here we report Li<sub>3</sub>ErI<sub>6</sub>, the first experimentally-obtained iodine-based compound within this material system of ionic conductors. Using a combination of synchrotron and neutron diffraction, we elucidate the structure, the lithium positions and possible diffusion pathways of Li<sub>3</sub>ErI<sub>6</sub>. Temperature-dependent impedance spectroscopy shows low activation energies of 0.37 and 0.38 eV alongside promising ionic conductivities of 0.65 mS·cm<sup>-1</sup> and 0.39 mS·cm<sup>-1</sup>directly after ball milling and the subsequently annealed Li<sub>3</sub>ErI<sub>6</sub>, respectively. Speed of sound measurements are used to determine the Debye frequency of the lattice as a descriptor of the lattice dynamics and overall lattice softness, and Li<sub>3</sub>ErI<sub>6</sub> is compared to the known material Li<sub>3</sub>ErCl<sub>6</sub>. The softer, more polarizable framework from the iodide anion leads to improved ionic transport, showing that the idea of softer lattices holds up in this class of materials. This work provides Li<sub>3</sub>ErI<sub>6</sub> as an interesting novel framework for optimization in the class of halide-based ionic conductors.</p>
Simulation of the lattice dynamics of Cu2Se and Cu2Te superionic conductors