Super SEI‐Forming Anion for Enhanced Interfacial Stability in Solid‐State Lithium Metal Batteries

The extremely high chemical reactivity of lithium metal (Li°) electrodes and its enormous volume change during repetitive cycles cause continuous interfacial degradations in prevailing organic electrolytes, thus deteriorating the cycling performances of rechargeable lithium metal batteries (LMBs). Herein, departing from traditional wisdom on the design of electrolyte components, a super SEI-forming anion (SSA), as an efficient percussor for building stable interphases on Li° electrode, is proposed. Comprehensive investigations related to the unique anion chemistry of SSA reveal that the sulfonate and polyfluoroalkyl functionalities synergistically contribute to uniform spatial distributions of designer interfacial species, greatly improving the surface coverage property and conformal ability of the resulting interphases. Consequently, the incorporation of SSA leads to significant improvements in the cyclability of Li° electrode (exceeding 575 mAh cm<sup>-2</sup> before failure) and the corresponding rechargeable Li°||LiFePO<sub>4</sub> cells [a five-time increase in lifespan as compared to the benchmark cell with the popular SEI-forming anion bis(fluorosulfonyl)imide (FSI)]. The present work offers a paradigm shift to tame the notorious interfacial issues via upgraded anion chemistry, which can promote the practical development of rechargeable LMBs and other kinds of metal batteries.

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Publication Details

Journal
Advanced Materials
Published
2024-10-09
DOI
https://doi.org/10.1002/adma.202410954
Citations
19
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
3.96

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article

Super SEI‐Forming Anion for Enhanced Interfacial Stability in Solid‐State Lithium Metal Batteries

Zhibin Zhou, Heng Zhang, Xuejie Huang, Hailong Yu et al.
19 citations
Advanced Materials
Advanced Battery Materials and Technologies
3.96
article

Super SEI‐Forming Anion for Enhanced Interfacial Stability in Solid‐State Lithium Metal Batteries

Zhibin Zhou, Heng Zhang, Xuejie Huang, Hailong Yu, Liubin Ben, Michel B. Armand, Ziyu Song, Jing Zhu, Mengyu Tian, Wenfang Feng, Jiayi Chen
article en
19 citations

Abstract

The extremely high chemical reactivity of lithium metal (Li°) electrodes and its enormous volume change during repetitive cycles cause continuous interfacial degradations in prevailing organic electrolytes, thus deteriorating the cycling performances of rechargeable lithium metal batteries (LMBs). Herein, departing from traditional wisdom on the design of electrolyte components, a super SEI-forming anion (SSA), as an efficient percussor for building stable interphases on Li° electrode, is proposed. Comprehensive investigations related to the unique anion chemistry of SSA reveal that the sulfonate and polyfluoroalkyl functionalities synergistically contribute to uniform spatial distributions of designer interfacial species, greatly improving the surface coverage property and conformal ability of the resulting interphases. Consequently, the incorporation of SSA leads to significant improvements in the cyclability of Li° electrode (exceeding 575 mAh cm<sup>-2</sup> before failure) and the corresponding rechargeable Li°||LiFePO<sub>4</sub> cells [a five-time increase in lifespan as compared to the benchmark cell with the popular SEI-forming anion bis(fluorosulfonyl)imide (FSI)]. The present work offers a paradigm shift to tame the notorious interfacial issues via upgraded anion chemistry, which can promote the practical development of rechargeable LMBs and other kinds of metal batteries.

Advanced MaterialsVol. 36(47)
Songshan Lake Materials Laboratory (CN), CIC energiGUNE (ES), Institute of Physics (CN), University of Chinese Academy of Sciences (CN), Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Responsible consumption and production
Openalex Percentile: Top 6%
Advanced Battery Materials and Technologies
3.96
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