Unravelling the Complex LiOH-Based Cathode Chemistry in Lithium-Oxygen Batteries

Abstract

The LiOH-based cathode chemistry has demonstrated potential for high-energy Li-O₂ batteries. However, the understanding of such complex chemistry remains incomplete. Herein, we use the combined experimental methods with ab initio calculations to study LiOH chemistry. We provide a unified reaction mechanism for LiOH formation during discharge via net 4 e^- oxygen reduction, in which Li₂ O₂ acts as intermediate in low water-content electrolyte but LiHO₂ as intermediate in high water-content electrolyte. Besides, LiOH decomposes via 1 e^- oxidation during charge, generating surface-reactive hydroxyl species that degrade organic electrolytes and generate protons. These protons lead to early removal of LiOH, followed by a new high-potential charge plateau (1 e^- water oxidation). At following cycles, these accumulated protons lead to a new high-potential discharge plateau, corresponding to water formation. Our findings shed light on understanding of 4 e^- cathode chemistries in metal-air batteries.

Keywords: Ab Initio Calculations; Four-Electron Oxygen Reduction; Isotopic Labeling; LiOH-Based Cathode Chemistry; Lithium−Oxygen Batteries; Reactive Oxygen Species.