Deciphering the Origin of Interface-Induced High Li and Na Ion Conductivity in Nanocomposite Solid Electrolytes Using X-Ray Raman Spectroscopy

Solid-state electrolytes (SSEs) with high ionic conductivities are crucial for safer and high-capacity batteries. Interface effects in nanocomposites of SSEs and insulators can lead to profound increases in conductivity. Understanding the composition of the interface is crucial for tuning the conductivity of composite solid electrolytes. Herein, X-ray Raman Scattering (XRS) spectroscopy is used for the first time to unravel the nature of the interface effects responsible for conductivity enhancements in nanocomposites of complex hydride-based electrolytes (LiBH4, NaBH4, and NaNH2) and oxides. XRS probe of the Li, Na, and B local environments reveals that the interface consists of highly distorted/defected and structurally distinct phase(s) compared to the original compounds. Interestingly, nanocomposites with higher concentrations of the interface compounds exhibit higher conductivities. Clear differences are observed in the interface composition of SiO2- and Al2O3-based nanocomposites, attributed to differences in the reactivity of their surface groups. These results demonstrate that interfacial reactions play a dominant role in conductivity enhancement in composite solid electrolytes. This work showcases the potential of XRS in investigating interface interactions, providing valuable insights into the often complex ion conductor/insulator interfaces, especially for systems containing light elements such as Li, B, and Na present in most SSEs and batteries. X-ray Raman spectroscopy is employed to unravel the nature of the interface in nanocomposites of complex hydrides and metal oxides, and thereby the origin of the profound increase in ionic conductivity in these nanocomposite solid electrolytes. The results reveal that surface reactions at ion conductor-insulator interfaces play a dominant role in interfacial ion transport.image