4.6 Article

Electrochemical Quantification of Lithium Plating: Challenges and Considerations

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 166, Issue 12, Pages A2689-A2696

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/2.1581912jes

Keywords

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Funding

  1. Vehicle Technologies Office of the U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy under the Advanced Battery Cell Research Program (eXtreme Fast Charge Cell Evaluation of Lithium-ion Batteries, XCEL)
  2. U.S. Department of Energy [AC07-05ID14517]

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Low-level overlithiation (1.5 to 5.5% based on the theoretical capacity of graphite, 372 mAh(-1)) behavior of graphite electrode is reported to illustrate the challenges of detecting Li plating via electrochemical methods such as voltage, incremental capacity (dQ.dV(-1)), and coulombic efficiency. Low-level overlithiation is closely tied to multiple in-vehicle mild-abuse and aging-related conditions such as overcharge and fast-charge where early detection of plating is highly desirable. Analysis following overlithiation includes the interplay between reversibly and irreversibly plated Li with and without rest after overlithiation, impacts on the electrode, and the feasibility of using reversible Li stripping as a detection method. Following overlithiation the capacity for graphite readily approaches theoretical values. Inspection of the lithiation voltage profile suggests that a portion of this capacity is associated with the chemical lithiation of graphite and effectively suppresses the dQ.dV(-1) signal related to Li stripping. Analysis of coulombic efficiency and the lithiation and delithiation profiles are used to quantify the capacity of graphite, irreversibly and reversibly plated lithium. It has been found that the extent of reversibility of lithium plating is distinctly impacted by rest with periods as short as one hour reducing the extent of reversibility and hence electrochemical detection. (C) The Author(s) 2019. Published by ECS.

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