High-Temperature Chemical Oxidation Pathways in Lithium-ion Batteries: Mechanistic insights into Ethylene Carbonate Decomposition

Abstract

A thermal event remains a safety challenge for lithium-ion batteries due to the selfreinforcing nature of the exothermic reactions occurring at elevated temperatures. Higher states of charge have been shown to exacerbate the onset and severity of a thermal event. For cells containing Ni-rich layered oxide-based electrodes, this has been attributed to the increased instability of the material leading to lattice oxygen release. The degradation reactions on the electrode/electrolyte interface triggered by this oxygen remain insufficiently understood. In this study, we investigate high-temperature degradation pathways of ethylene carbonate (EC)-based electrolytes in contact with Ni-rich positive electrode active materials up to 130 °C. By combining in-situ high-temperature online electrochemical mass spectrometry with post-mortem analyses, we identify and validate key degradation intermediates and products. Two distinct EC oxidation pathways are revealed: one activated at high voltages, and the other one initiated by traces of water impurities. Complementary density functional theory calculations show the reactions are thermodynamically favorable and quantify the heat release associated with each pathway. Both pathways produce significant heat and lead to gassing of CO₂ and H₂ . These findings suggest significant contribution of EC to thermal gas evolution and exothermicity under abuse conditions, thereby establishing a mechanistic link between electrolyte chemistry and thermal events. This integrated experimental-computational approach provides critical insights to guide improved electrolyte formulations and predictive thermal models.