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Interface Stability and Reaction Mechanisms of Li3YCl5Br with High-Voltage Cathodes and Li Metal Anode: Insights from
Andrey Golov1, Jian Xiang Lian1, Javier Carrasco1,2
1Centre for Cooperative Research on Alternative Energies (CIC energiGUNE), Basque Research and Technology Alliance (BRTA), 01510 Vitoria-Gasteiz, Spain.
Abstract:
Recent advancements in battery technology emphasize the critical role of solid electrolytes in enhancing the performance and safety of next-generation batteries. In this study, we investigate the interface stability and reaction mechanisms of Li3YCl5Br, a promising halide-based solid electrolyte, in contact with high-voltage Ni-Mn-Co (NMC) cathodes and a Li metal anode using ab initio molecular dynamics simulations. Our findings reveal that Li3YCl5Br reacts with charged NMC cathodes. This reaction involves changes in the oxidation states of Br- anions in Li3YCl5Br and d-element cations in NMC, as well as the diffusion of Li ions from the solid electrolyte to the cathode to maintain charge balance. The reaction is confined to the interface, suggesting bulk stability. Conversely, the Li/Li3YCl5Br interface exhibits significant instability, with a chemical reaction that results in substantial structural changes and the formation of LiCl and LiBr at the solid electrolyte surface and metallic Y at the Li anode surface. These insights provide valuable information for optimizing interfacial design, aiming at improving the performance and reliability of all-solid-state batteries using halide solid electrolytes.
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