On the Discrepancy between Local and Average Structure in the Fast Na plus Ionic Conductor Na2.9Sb0.9W0.1S4

Aliovalent substitution is a common strategy to improve the ionic conductivity of solid electrolytes for solid-state batteries. The substitution of SbS43- by WS42- in Na2.9Sb0.9W0.1S4 leads to a very high ionic conductivity of 41 mS cm-1 at room temperature. While pristine Na3SbS4 crystallizes in a tetragonal structure, the substituted Na2.9Sb0.9W0.1S4 crystallizes in a cubic phase at room temperature based on its X-ray diffractogram. Here, we show by performing pair distribution function analyses and static single-pulse 121Sb NMR experiments that the short-range order of Na2.9Sb0.9W0.1S4 remains tetragonal despite the change in the Bragg diffraction pattern. Temperature-dependent Raman spectroscopy revealed that changed lattice dynamics due to the increased disorder in the Na+ substructure leads to dynamic sampling causing the discrepancy in local and average structure. While showing no differences in the local structure, compared to pristine Na3SbS4, quasi-elastic neutron scattering and solid-state 23Na nuclear magnetic resonance measurements revealed drastically improved Na+ diffusivity and decreased activation energies for Na2.9Sb0.9W0.1S4. The obtained diffusion coefficients are in very good agreement with theoretical values and long-range transport measured by impedance spectroscopy. This work demonstrates the importance of studying the local structure of ionic conductors to fully understand their transport mechanisms, a prerequisite for the development of faster ionic conductors.

Automated summary

Aliovalent substitution is an effective strategy to improve the ionic conductivity of solid electrolytes. Substituting SbS43- with WS42- in Na2.9Sb0.9W0.1S4 significantly enhances its ionic conductivity, reaching 41 mS cm-1 at room temperature. Despite the change in the diffraction pattern, the short-range order of Na2.9Sb0.9W0.1S4 remains tetragonal. The study highlights the importance of analyzing the local structure of ionic conductors to understand their transport mechanisms and develop faster ionic conductors.