Beneficial vs. Inhibiting Passivation by the Native Lithium Solid Electrolyte Interphase Revealed by Electrochemical Li+ Exchange

10 May 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.


Despite being a leading candidate to meet stringent energy targets of Li-ion batteries, the lithium (Li) metal anode has yet to achieve Coulombic efficiency (CE) requirements for long cycle life (>99.9%), particularly at high rates (>1 C). These limitations derive from the native solid electrolyte interphase (SEI) which, among multiple functions, stabilizes and protects deposited Li. The SEI also plays a critical role in regulating Li+ exchange between the electrolyte and the electrode, but quantification of this effect has been non-straightforward, and a general relationship between Li+ exchange and CE has not been clearly elucidated to date. Using electrochemical impedance and voltammetry, we report self-consistent Li+ exchange values of native SEIs over a range of relevant electrolytes with CE spanning 78.0% to >99%. CE and its retention at high rates are found to be positively correlated with the rate of SEI Li+ exchange. Additionally, Li+ exchange rates increased during cycling in high-CE electrolytes, in some cases by an order of magnitude to exceed 10 mA/cm2, whereas for low-CE electrolytes they remained low (<1 mA/cm2), revealing a chemistry-dependent picture of SEI evolution with often-complex dynamics. The evolution in Li+ exchange unique to high-CE electrolytes also provides insights into the role and effectiveness of the formation cycle on Cu current collectors upon the first plating step. Altogether, these findings indicate that Li+ exchange governs several key processes related to Li deposition and cycling efficiency. Consequently, its quantification can help to guide future high-CE electrolyte design, particularly targeting high rates (>1 mA/cm2). 


solid electrolyte interphase
exchange current
lithium anode

Supplementary materials

Electronic Supplementary Information
Supplementary methods, figures (S1-20), notes (1-4) and references accompanying the main text.


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