Electrolyte Li <sup>+</sup> Chemical Potential Correlates with Graphite Negative Electrode Reactions in Lithium‐Ion Batteries
Abstract
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 + intercalation into graphite negative electrodes. In commercial LIBs, this reaction is reversible in ethylene carbonate (EC) electrolytes, whereas unfavorable Li + –solvent cointercalation occurs in many other electrolytes. Recently, EC‐free Li + 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 + intercalation or Li + –solvent cointercalation occurs has yet to be identified. Herein, the electrolyte Li + chemical potential is reported as a quantitative descriptor of the Li + intercalation behavior. Solvent cointercalation is generally inhibited above a certain threshold of the electrolyte Li + chemical potential. This work provides a novel guideline for designing advanced LIB electrolytes.
Article Details
Authors (8)
Yasuyuki Kondo
Haruna Nakajima
SANKEN The University of Osaka Ibaraki Osaka 567‐0047 Japan
Yu Katayama
SANKEN, Osaka University, Mihogaoka, Ibaraki 5670047, Japan
Nao Kobayashi
Shinya Otani
Chemicals Division Daikin Industries, Ltd. Settsu Osaka 566‐8585 Japan
Akinori Tani
Chemicals Division Daikin Industries, Ltd. Settsu Osaka 566‐8585 Japan
Shigeaki Yamazaki
Chemicals Division Daikin Industries, Ltd. Settsu Osaka 566‐8585 Japan
Yuki Yamada
SANKEN The University of Osaka Ibaraki Osaka 567‐0047 Japan