biostudies-literatureSebti EU.S. Department of EnergyMinistry of Education - SingaporeNational Research Foundation SingaporeNational Research CouncilNational Science Foundation5795-5811https://www.ebi.ac.uk/biostudies/studies/S-EPMC8991002biostudies-literatureUnknown144(13)In the pursuit of urgently needed, energy dense solid-state batteries for electric vehicle and portable electronics applications, halide solid electrolytes offer a promising path forward with exceptional compatibility against high-voltage oxide electrodes, tunable ionic conductivities, and facile processing. For this family of compounds, synthesis protocols strongly affect cation site disorder and modulate Li⁺ mobility. In this work, we reveal the presence of a high concentration of stacking faults in the superionic conductor Li₃YCl₆ and demonstrate a method of controlling its Li⁺ conductivity by tuning the defect concentration with synthesis and heat treatments at select temperatures. Leveraging complementary insights from variable temperature synchrotron X-ray diffraction, neutron diffraction, cryogenic transmission electron microscopy, solid-state nuclear magnetic resonance, density functional theory, and electrochemical impedance spectroscopy, we identify the nature of planar defects and the role of nonstoichiometry in lowering Li⁺ migration barriers and increasing Li site connectivity in mechanochemically synthesized Li₃YCl₆. We harness paramagnetic relaxation enhancement to enable ⁸⁹Y solid-state NMR and directly contrast the Y cation site disorder resulting from different preparation methods, demonstrating a potent tool for other researchers studying Y-containing compositions. With heat treatments at temperatures as low as 333 K (60 °C), we decrease the concentration of planar defects, demonstrating a simple method for tuning the Li⁺ conductivity. Findings from this work are expected to be generalizable to other halide solid electrolyte candidates and provide an improved understanding of defect-enabled Li⁺ conduction in this class of Li-ion conductors.Journal of the American Chemical SocietyStacking Faults Assist Lithium-Ion Conduction in a Halide-Based Superionic Conductor.PMC8991002DE-AC05-76RLO1830DMR 1720256NRFF12-2020-00121650114R-284-000-186-133Wang CRichardson PMGiovine RGonzalez-Correa EBrown CMKoirala KPChen HClement RJSebti EWhite KMCanepa PEvans HACheetham AKXu YfalseStacking Faults Assist Lithium-Ion Conduction in a Halide-Based Superionic Conductor.In the pursuit of urgently needed, energy dense solid-state batteries for electric vehicle and portable electronics applications, halide solid electrolytes offer a promising path forward with exceptional compatibility against high-voltage oxide electrodes, tunable ionic conductivities, and facile processing. For this family of compounds, synthesis protocols strongly affect cation site disorder and modulate Li⁺ mobility. In this work, we reveal the presence of a high concentration of stacking faults in the superionic conductor Li₃YCl₆ and demonstrate a method of controlling its Li⁺ conductivity by tuning the defect concentration with synthesis and heat treatments at select temperatures. Leveraging complementary insights from variable temperature synchrotron X-ray diffraction, neutron diffraction, cryogenic transmission electron microscopy, solid-state nuclear magnetic resonance, density functional theory, and electrochemical impedance spectroscopy, we identify the nature of planar defects and the role of nonstoichiometry in lowering Li⁺ migration barriers and increasing Li site connectivity in mechanochemically synthesized Li₃YCl₆. We harness paramagnetic relaxation enhancement to enable ⁸⁹Y solid-state NMR and directly contrast the Y cation site disorder resulting from different preparation methods, demonstrating a potent tool for other researchers studying Y-containing compositions. With heat treatments at temperatures as low as 333 K (60 °C), we decrease the concentration of planar defects, demonstrating a simple method for tuning the Li⁺ conductivity. Findings from this work are expected to be generalizable to other halide solid electrolyte candidates and provide an improved understanding of defect-enabled Li⁺ conduction in this class of Li-ion conductors.2022-01-01T00:00:00Z2022 Apr2025-04-04T21:33:17.715Z2025-04-04T21:33:17.715ZS-EPMC89910023532553410.1021/jacs.1c11335