Advancing lithium metal electrode beyond 99.9% coulombic efficiency via super-saturated electrolyte with compressed solvation structure

Lithium metal negative electrode is pivotal for advancing high-energy-density lithium batteries. Despite their promise, the inherent poor interfacial stability of electrolytes on lithium metal and the repeated reconstruction of the solid electrolyte interphase lead to continuous consumption of active Li and electrolyte, causing rapid failure of Li metal batteries under practical conditions. Here, we propose compressing the spacing between Li ions and anions to recruit more anions around Li ions, forming tighter solvation clusters, and then achieving the super-saturated electrolyte with a 16 M Li salt concentration in the solvent phase. This compressed solvation structure electrolyte demonstrates enhanced stability towards Li metal negative electrode, attaining more than 99.9% coulombic efficiency in Li||Cu cells and enabling long cycling life in lean-Li Li metal full cells. Designed with a positive electrode material proportion of 68%, our Li metal pouch cell achieves a specific energy of 510.3 Wh kg<sup>-1</sup> (based on the total mass of the cell) and maintains stable cycling over 100 cycles.

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Publication Details

Journal
Nature Communications
Published
2025-05-07
DOI
https://doi.org/10.1038/s41467-025-59563-y
Citations
33
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
24.10

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article

Advancing lithium metal electrode beyond 99.9% coulombic efficiency via super-saturated electrolyte with compressed solvation structure

Aoyuan Chen, Haoshen Zhou, Ping He, Wujie Yang
33 citations
Nature Communications
Advanced Battery Materials and Technologies
24.10
article

Advancing lithium metal electrode beyond 99.9% coulombic efficiency via super-saturated electrolyte with compressed solvation structure

Aoyuan Chen, Haoshen Zhou, Ping He, Wujie Yang
article en
33 citations

Abstract

Lithium metal negative electrode is pivotal for advancing high-energy-density lithium batteries. Despite their promise, the inherent poor interfacial stability of electrolytes on lithium metal and the repeated reconstruction of the solid electrolyte interphase lead to continuous consumption of active Li and electrolyte, causing rapid failure of Li metal batteries under practical conditions. Here, we propose compressing the spacing between Li ions and anions to recruit more anions around Li ions, forming tighter solvation clusters, and then achieving the super-saturated electrolyte with a 16 M Li salt concentration in the solvent phase. This compressed solvation structure electrolyte demonstrates enhanced stability towards Li metal negative electrode, attaining more than 99.9% coulombic efficiency in Li||Cu cells and enabling long cycling life in lean-Li Li metal full cells. Designed with a positive electrode material proportion of 68%, our Li metal pouch cell achieves a specific energy of 510.3 Wh kg<sup>-1</sup> (based on the total mass of the cell) and maintains stable cycling over 100 cycles.

Nature CommunicationsVol. 16(1)
Nanjing Tech University (CN), Collaborative Innovation Center of Advanced Microstructures (CN), Nanjing University (CN)
National Natural Science Foundation of China
Affordable and clean energy
Openalex Percentile: Top 0%
Advanced Battery Materials and Technologies
24.10
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