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, Ecorr, and current densities, jcorr, 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 jcorr, as shown in Figure 1, whereas additives that increased DFPH generation had no apparent effect.
References:
[1] Myung, Hitoshi, and Sun. J. Mater. Chem., 2011, 21, 9891-9911.
[2] Ma et al. J. Phys. Chem. Lett. 2017, 8, 5, 1072–1077
[3] Wiemers-Meyer, Winter, and Nowak. Phys. Chem. Chem. Phys., 2016, 18, 26595-26601.
Figure 1: Bar graph of corrosion current, jcorr, measured for a LiPF6/EC/DMC (15/25/60 wt%) control electrolyte with 2500 ppm of water contamination, as well as with ~2 wt% of an additive that formed more DFPH than the control, an additive that formed more DFPH and HF than the control, and an additive that scavenged HF. Inset: Optical image of the inside of a mild steel can disassembled after 14 days of 60°C storage at top of charge illustrating dark regions indicative of steel corrosion.