(Digital Presentation) Evaluating the Corrosivity of Liquid LiPF6 Electrolytes with Nickel-Coated Mild Steel Used in the Manufacturing of Li-Ion Cells for Energy Storage

Abstract

Effects of electrolyte degradation on cell performance and corrosion of cell components, e.g. current collectors, are topics that have been reported in the literature.1,2 Recently, it has been reported that water contamination of LiPF6 liquid electrolytes can lead to salt degradation, generating difluorophosphoric acid (DFPH) and hydrofluoric acid (HF).3 With strict quality control of the moisture content in individual components and the use of dryroom conditions for cell assembly the risk of moisture contamination can be practically eliminated. When moisture is allowed to enter the cell in controlled research samples, dark stains indicative of pitting type corrosion have been observed on the inside of mild steel cans that are used to house cylindrically wound electrodes (see Figure 1 inset). Motivation to understand the underlying corrosion mechanism and the influential factors is important to help lower the risk of occurrence in manufacturing further.The use of a simple corrosion plate cell to study the susceptibility of a mild steel sample immersed in a LiPF6/EC/DMC (15/25/60 wt%) electrolyte will be discussed, with a focus on measured corrosion potentials, E corr, and current densities, j corr, extracted from the Tafel region of a potentiodynamic scan. Observations on the influence of acid degradation products in the electrolyte on the corrosion susceptibility of the mild steel will be discussed and applied to study select electrolyte additives previously reported in literature. Early results have shown that additives that scavenge HF and/or water directly can effectively suppress j corr, as shown in Figure 1, whereas additives that increased DFPH generation had no apparent effect.