电解质
锂(药物)
盐(化学)
离子
材料科学
无机化学
化学工程
化学
电极
有机化学
医学
工程类
内科学
物理化学
作者
Louis Hartmann,Lennart Reuter,Lea Wallisch,Anton Beiersdorfer,Alexander Adam,Daniel Goldbach,Tobias Teufl,Peter Lamp,Hubert A. Gasteiger,Johannes Wandt
标识
DOI:10.1149/1945-7111/ad4821
摘要
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 LiPF 6 salt in the electrolyte. For this, we analyze the LiPF 6 concentration in aged cells, the generation of H 2 upon storage, and the cell resistance for different aging conditions. We show that the LiPF 6 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, LiPF 6 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 LiPF 6 loss change the cyclable lithium inventory of a lithium-ion cell.
科研通智能强力驱动
Strongly Powered by AbleSci AI