Evidence for a Solid-Electrolyte Inductive Effect in Superionic Conductors

Identifying and optimizing highly-conducting lithium-ion solid electrolytes is a critical step towards the realization of commercial all–solid-state lithium-ion batteries. Strategies to enhance ionic conductivities in solid electrolytes typically focus on the effects of modifying their crystal structures or of tuning mobile-ion stoichiometries. A less-explored approach is to modulate the chemical-bonding interactions within a material to promote fast lithium-ion diffusion. Recently, the idea of a solid-electrolyte inductive effect was proposed, whereby changes in bonding within the solid-electrolyte host-framework modify the potential-energy landscape for the mobile ions, resulting in an enhanced ionic conductivity. This concept has since been invoked to explain anomalous conductivity trends in a number of solid electrolytes. Direct evidence for a solid-electrolyte inductive effect, however, is lacking—in part because of the challenge of quantifying changes in local bonding interactions within a solid-electrolyte host-framework. Here, we consider the evidence for a solid-electrolyte inductive effect in the archetypal superionic lithium-ion conductor Li 10 Ge 1− x Sn x P 2 S 12 , using Rietveld refinements against high-resolution temperature-dependent neutron-diffraction data, Raman spectroscopy, and density functional theory calculations. Substituting Ge for Sn weakens the {Ge,Sn}–S bonding interactions and increases the charge-density associated with the S 2- ions. This charge redistribution modifies the Li + substructure causing Li + ions to bind more strongly to the host-framework S anions; which in turn modulates the Li-ion potential-energy surface, increasing local barriers for Li-ion diffusion. Each of these effects is consistent with the predictions of the solid-electrolyte inductive effect model. Density functional theory calculations further predict that this inductive effect occurs even in the absence of changes to the host-framework geometry due to Ge → Sn substitution. These results provide direct evidence in support of a measurable solid-electrolyte inductive effect and demonstrate its application as a practical strategy for tuning ionic conductivities in superionic lithium-ion conductors.