Abstract
We test the stability of pre-lithiated graphite anodes for Li-ion batteries in a dry room battery processing room. The reaction between LiCx and laboratory air was followed using operando NMR and x-ray diffraction, as these methods are sensitive to change in Li stoichiometry in graphite. There is minimal reactivity between LiC6 and N2, CO2 or O2; however, LiC6 reacts with moisture to form lithium (hydr)oxide. The reaction rate follows zero-order kinetics with respects to intercalated lithium suggesting that lithium transport through the graphite is fast. The reaction occurs by sequential formation of higher stages-LiC12, then LiC18, and then LiC24-as the hydrolysis proceeds to the formation of LixOHy and graphite end products. Slowing down the formation rate of the LixOHy passivation layer stabilizes of the higher stages.
Original language | English |
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Pages (from-to) | 253-260 |
Number of pages | 8 |
Journal | Journal of Power Sources |
Volume | 287 |
DOIs | |
State | Published - Aug 1 2015 |
Funding
Research was supported by the Fluid Interface Reactions, Structures, and Transport (FIRST) Center, an Energy Frontier Research Center funded by the U.S. Department of Energy , Office of Science, Office of Basic Energy Sciences (RLS, NJD, EH). We thank Michael A. McGuire (ORNL) for assistance in performing the XRD measurements and analysis. We also thank Pred Materials International for the MGP-A.
Funders | Funder number |
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U.S. Department of Energy | |
Office of Science | |
Basic Energy Sciences |
Keywords
- Battery processing
- Li NMR
- Lithium intercalation
- Solid electrolyte interphase
- Solid-state synthesis