No abstract

Solid electrolytes are generating considerable interest for all-solid-state Li-ion batteries to address safety and performance issues. Grain boundaries have a significant influence on solid electrolytes and are key hurdles that must be overcome for their successful application. However, grain boundary effects on ionic transport are not fully understood, especially at the atomic scale. The Li-rich anti-perovskite LiOCl is a promising solid electrolyte, although there is debate concerning the precise Li-ion migration barriers and conductivity. Using LiOCl as a model polycrystalline electrolyte, we apply large-scale molecular dynamics simulations to analyze the ionic transport at stable grain boundaries. Our results predict high concentrations of grain boundaries and clearly show that Li-ion conductivity is severely hindered through the grain boundaries. The activation energies for Li-ion conduction traversing the grain boundaries are consistently higher than that of the bulk crystal, confirming the high grain boundary resistance in this material. Using our results, we propose a polycrystalline model to quantify the impact of grain boundaries on conductivity as a function of grain size. Such insights provide valuable fundamental understanding of the role of grain boundaries and how tailoring the microstructure can lead to the optimization of new high-performance solid electrolytes.

Combined computational and experimental examination of lithium-ion and proton dynamics in next-generation anti-perovskite solid electrolytes.

Lattice compression through hydrostatic pressure has emerged as an effective means of tuning the structural and optoelectronic properties of hybrid halide perovskites. In addition to external pressure, the local strain present in solution-processed thin films also causes significant heterogeneity in their photophysical properties. However, an atomistic understanding of structural changes of hybrid perovskites under pressure and their effects on the electronic landscape is required. Here, we use high level ab initio simulation techniques to explore the effect of lattice compression on the formamidinium (FA) lead iodide compound, FA1–x Cs x PbI3 (x = 0, 0.25). We show that, in response to applied pressure, the Pb–I bonds shorten, the PbI6 octahedra tilt anisotropically, and the rotational dynamics of the FA+ molecular cation are partially suppressed. Because of these structural distortions, the compressed perovskites exhibit band gaps that are narrower (red-shifted) and indirect with spin-split band edges. Furthermore, the shallow defect levels of intrinsic iodide defects transform to deep-level states with lattice compression. This work highlights the use of hydrostatic pressure as a powerful tool for systematically modifying the photovoltaic performance of halide perovskites.