Unveiling the structure and ion dynamics of amorphous Na3-xOHxCl antiperovskite electrolytes by first-principles molecular dynamics

Sodium oxyhalide and hydroxyhalide antiperovskites are promising solid-state electrolytes (SSEs) because of their low melting point and rapid synthesis and, as such, they are becoming competitive with respect to other systems. While the structure and the mechanism underlying the ion dynamics are increasingly well understood in crystalline antiperovskites, their amorphous counterpart lacks precise structural characterization, hampering any conclusive insight into their properties. In this work, we resort to first-principles molecular dynamics within the Car-Parrinello scheme to assess the structure and ion dynamics of amorphous Na3-xOHxCl (with x = 0, 0.5, and 1) antiperovskites at a quantitative level. We obtain a detailed structural description of these amorphous systems, unveiling the mechanism inherent to the dynamics of Na ions, the role of H atoms, and the resulting ionic conductivity. Our results demonstrate that the structure of amorphous Na3OCl significantly differs from its crystal phase, showing very limited intermediate-range order and a short-range order mainly driven by four-fold Na atoms. Our results reveal that there is no evidence of phase separation in the amorphous Na3-xOHxCl, unlike the previous conjectured model of glassy Li3OCl. The amorphous structure of Na3OCl features remarkable Na ion dynamics and ionic conductivity, rivaling that of defective crystalline phases and highlighting its potential as a promising solid-state electrolyte. In hydroxylated models, the presence of hydroxyl OH- anions plays a crucial role in the mobility of Na ions. This is facilitated by the rapid rotation of O-H bonds and paddlewheel-type mechanisms, leading to enhanced ion mobility in the amorphous Na3-xOHxCl systems. This work provides unprecedented physical and chemical insight into the interplay between the structure, bonding, and ion transport in amorphous sodium-rich oxyhalide and hydroxyhalide antiperovskites, paving the way to their practical realization in next-generation SSEs.

Automated summary

This study investigates the structure and ion dynamics of amorphous sodium oxyhalide and hydroxyhalide antiperovskites using first-principles molecular dynamics. The results demonstrate the differences between the amorphous and crystalline structures and reveal the remarkable ion dynamics and conductivity of sodium oxyhalide. The presence of hydroxyl anions plays a crucial role in the mobility of sodium ions in hydroxyhalide systems.