Electrode potential influences the reversibility of lithium-metal anodes
Seongjae Ko,
Tomohiro Obukata,
Tatau Shimada,
Norio Takenaka,
Masanobu Nakayama,
Atsuo Yamada () and
Yuki Yamada ()
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Seongjae Ko: The University of Tokyo
Tomohiro Obukata: The University of Tokyo
Tatau Shimada: The University of Tokyo
Norio Takenaka: The University of Tokyo
Masanobu Nakayama: Nagoya Institute of Technology
Atsuo Yamada: The University of Tokyo
Yuki Yamada: The University of Tokyo
Nature Energy, 2022, vol. 7, issue 12, 1217-1224
Abstract:
Abstract Lithium-metal batteries are a promising technology to address the emerging demand for high-energy-density storage systems. However, their cycling encounters a low Coulombic efficiency (CE) due to the unceasing electrolyte decomposition. Improving the stability of solid electrolyte interphase (SEI) suppresses the decomposition and increases CE. However, SEI morphology and chemistry alone cannot account for CE, and a full explanation is still lacking. Here we report that in diverse electrolytes, the large shift (>0.6 V) in the Li electrode potential and its association with the Li+ coordination structure influence the CE. Machine learning regression analysis and vibrational spectroscopy revealed that the formation of ion pairs is essential for upshifting the Li electrode potential, that is, for weakening the reducing ability of Li, which would lead to a high CE with diminished electrolyte decomposition. Various electrolytes with enhanced ion-pairing solution structure are designed to enable a significantly improved CE (>99%).
Date: 2022
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natene:v:7:y:2022:i:12:d:10.1038_s41560-022-01144-0
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DOI: 10.1038/s41560-022-01144-0
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