Electrolyte Li<sup>+</sup> Chemical Potential Correlates with Graphite Negative Electrode Reactions in Lithium-Ion Batteries.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41137642.
- Also identified by DOI 10.1002/adma.202514060 and PMC identifier 12822524.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Novel electrolytes for advanced lithium-ion batteries (LIBs) with higher energy density and safety are being extensively explored. A major challenge in developing new electrolytes is achieving reversible Li<sup>+</sup> intercalation into graphite negative electrodes. In commercial LIBs, this reaction is reversible in ethylene carbonate (EC) electrolytes, whereas unfavorable Li<sup>+</sup>-solvent cointercalation occurs in many other electrolytes. Recently, EC-free Li<sup>+</sup> intercalation has been achieved in some types of advanced electrolytes, including (localized) highly concentrated electrolytes and weakly coordinating electrolytes. However, an essential factor that dominates whether Li<sup>+</sup> intercalation or Li<sup>+</sup>-solvent cointercalation occurs has yet to be identified. Herein, the electrolyte Li<sup>+</sup> chemical potential is reported as a quantitative descriptor of the Li<sup>+</sup> intercalation behavior. Solvent cointercalation is generally inhibited above a certain threshold of the electrolyte Li<sup>+</sup> chemical potential. This work provides a novel guideline for designing advanced LIB electrolytes.