Depletion of Electrolyte Salt Upon Calendaric Aging of Lithium-Ion Batteries and its Effect on Cell Performance

Abstract

Abstract The trend for increased nickel content in layered transition metal oxide cathode active materials and increasing charging cut-off voltages aggravates aging of lithium-ion battery cells at high state of charge (SOC). We investigate the calendaric aging behavior of large-format automotive prototype cells and laboratory single-layer pouch cells at high but realistic cell voltages/SOCs and demonstrate that electrolyte oxidation in combination with follow-up reactions can cause a significant loss of the LiPF6 salt in the electrolyte. For this, we analyze the LiPF6 concentration in aged cells, the generation of H2 upon storage, and the cell resistance for different aging conditions. We show that the LiPF6 loss is a critical aging phenomenon, as it cannot readily be detected by capacity fading measurements at low/medium C-rates or by cell resistance measurements, while it severely reduces rate and fast-charging capability. Under certain circumstances, LiPF6 loss can even lead to a temporary capacity increase due to conversion of the conducting salt in the electrolyte to cyclable lithium in the active material. Finally, we suggest a possible reaction mechanism and a simple accounting model to keep track of how different side reactions involved in LiPF6 loss change the cyclable lithium inventory of a lithium-ion cell.