Understanding the relationship between structure, ionic conductivity, and synthesis is the key to the development of superionic conductors. Here, a series of Li3-3xM1+xCl6 (−0.14 < x ≤ 0.5, M = Tb, Dy, Ho, Y, Er, Tm) solid electrolytes with orthorhombic and trigonal structures are reported. The orthorhombic phase of Li–M–Cl shows an approximately one order of magnitude increase in ionic conductivities when compared to their trigonal phase. Using the Li–Ho–Cl components as an example, their structures, phase transition, ionic conductivity, and electrochemical stability are studied. Molecular dynamics simulations reveal the facile diffusion in the z-direction in the orthorhombic structure, rationalizing the improved ionic conductivities. All-solid-state batteries of NMC811/Li2.73Ho1.09Cl6/In demonstrate excellent electrochemical performance at both 25 and −10 °C. As relevant to the vast number of isostructural halide electrolytes, the present structure control strategy guides the design of halide superionic conductors.@en

Lithium halide electrolytes with high ion conductivity and good cathode compatibility have shown great potential for solid-state batteries. Li3YBr6, with a conductivity of 0.39 mS/cm at room temperature, synthesized by mechanical milling (BM-Li3YBr6), which can be further increased by heat treatment. The annealing parameters are tailored to obtain pure Li3YBr6 (AN-Li3YBr6) with a higher conductivity of 3.31 mS/cm by annealing the BM-Li3YBr6 at 500 °C for 5 h. The higher conductivity of AN-Li3YBr6 compared to the previously-reported results is due to the lower activation energy. NMR and simulation results show that the lithium ion migration between Li-1 and Li-2 sites along the [001] direction is the major obstacle for lithium diffusion in AN-Li3YBr6. The K- and L3-edge X-ray absorption near-edge structure (XANES) of Y for BM-Li3YBr6 and AN-Li3YBr6 showed that Y exists with similar local structures. The increased vibrations of AN-Li3YBr6 due to increased temperatures increase the rate of lithium jumping from one site to another, yielding higher lithium ion mobility. Lithium nuclear density maps prove that the mobile lithium on the 4g(Li) site is more sensitive to the varying temperatures. Both BM- and AN-Li3YBr6 are incompatible with Li, however, an annealing process can improve the electrochemical stability. Both the experimental and simulation results confirm the anode incompatibility between In and AN-Li3YBr6. To mitigate the cathode and anode incompatibility with AN-Li3YBr6, a LiNbO3 coating layer and a Li5.7PS4.7Cl1.3 buffer layer are introduced at the cathode side and anode side, respectively, to assemble all-solid-state batteries with improved capacity and cyclability.@en

The ultrafast ionic conductivity of Li 6 PS 5 Br, which is higher than 1 mS cm -1 at room temperature, makes it an attractive candidate electrolyte for the all-solid-state Li-S battery. A simple synthesis route with an easy scale up process is critical for practical applications. In this work, the highest room temperature ionic conductivity (2.58 × 10 -3 S cm -1 ) of Li 6 PS 5 Br is obtained by an optimal annealing temperature in a simple solid-state reaction method. Neutron diffraction and XRD show that the origin of the highest ionic conductivity is due to the higher purity, smaller mean lithium ion jumps and the optimal Br ordering over 4a and 4c sites. All-solid-state Li-S batteries using a S-C composite cathode in combination with the optimized Li 6 PS 5 Br electrolyte and Li-In anode show high (dis)charge capacities. Different cycling modes (charge-discharge and discharge-charge) reveal that the capacity of the S-C-Li 6 PS 5 Br/Li 6 PS 5 Br/Li-In battery arises from both the active S-C composite and the Li 6 PS 5 Br in the cathode mixture. The contribution of the latter is verified from all-solid-state batteries using Li 6 PS 5 Br and its analogues as active materials. Ex situ XRD and electrochemical performance results show that the contribution of capacity from Li 6 PS 5 Br in the cathode mixture may be associated with the decomposition product Li 2 S, while the Li 6 PS 5 Br in the bulk solid electrolyte layer is stable during cycling. @en