Abstract
The corrosion/passivation phenomenon of Al and stainless steel with 1.25 M LiFSI in ethylene carbonate / ethyl methyl carbonate 30/70 wt% electrolyte was studied in coin cell and pouch cell settings. Our results showed that the LiFSI electrolyte can passivate Al foil in the normal cell operation voltage window 2.8 to 4.3 V. In contrast, no passivation behavior was observed for stainless steel with ever growing current response in cyclic voltammetry test. Corrosion produced Fe/Cr ions were detected on the anode side, which accelerated the electrolyte decomposition reaction. The LiFSI electrolyte was tested in 1.5 Ah pouch cell for long term cycling performance and fast charging capabilities. The capacity retentions after 1000 cycles were 88.5% and 80% for ± 1C and extreme fast charging rates, which demonstrated the suitability of using LiFSI in Li-ion cells without stainless steel components.
Original language | English |
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Article number | 107088 |
Journal | Electrochemistry Communications |
Volume | 129 |
DOIs | |
State | Published - Aug 2021 |
Funding
This research at Oak Ridge National Laboratory , managed by UT Battelle, LLC, for the U.S. Department of Energy (DOE) under contract DE-AC05-00OR22725, was sponsored by the Office of Energy Efficiency and Renewable Energy (EERE) Vehicle Technologies Office (VTO) (Technology Manager: Brian Cunningham).
Funders | Funder number |
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U.S. Department of Energy | DE-AC05-00OR22725 |
Office of Energy Efficiency and Renewable Energy | |
Oak Ridge National Laboratory | |
UT-Battelle |
Keywords
- Corrosion
- Extreme fast charing
- LiFSI
- Stainless steel