Triggering dynamically disordered lithium sublattice in superionic conductors

The design of superionic conductors has been largely focused on static structural features, with the dynamic ion transport mechanism less explored. Here, we explore a paradigm that harnesses the polyanion rotations to trigger the dynamically disordered Li sublattice as well as the liquid-like cation diffusion for superior ionic conductivity in crystals. A descriptor called rotation tolerance factor was proposed as a predictive metric for identifying the potential fast-rotating anion clusters with the low mass and reduced valence charge for given structural frameworks. Guided by this factor, halides with rotational polyanions, namely Li3Y(SH)6, Li3Y(NH2)6, Li2Zr(NH2)6, and an oxide (Li6.5La3Zr2O11.5(NH2)0.5) have been designed with synergistic polyanion rotation and Li⁺ sublattice disorder, which lead to enhanced Li ionic conductivities at room temperature compared to the counterparts without polyanions. The experimentally synthesized NH2- incorporated Li2ZrCl5.92(NH2)0.08 demonstrates a four-fold higher conductivity over Li2ZrCl6 control, enabling all-solid-state Li-In | |LiCoO2 and Li-In | |LiNi0.88Co0.09Mn0.03O2 cells with 96.5% and 97.4% capacity retention after 190 cycles at 140 and 200 mA g-1, respectively. This work provides an insight that flexible anion rotations could promote the dynamically disordered lithium sublattice distribution as well as the ionic conductivity. Superionic conductors are typically engineered from static crystal structures. Here, authors present how flexible polyanion rotations induce dynamic disorder in lithium sublattice, enabling liquid-like ion diffusion and enhanced ionic conductivity.