Enhancing Efficiency, Stability, and Cycle Life of Lithium Metal Electrodeposition in Dry Solid-State Polymer Electrolytes

Dry solid polymer electrolytes (SPEs), particularly those based on poly(ethylene oxide) (PEO), hold significant potential for advancing solid-state Li-metal battery (LMB) technology. Despite extensive research over the years, a comprehensive evaluation of Coulombic efficiency (CE), deposit stability, and cycle life for reversible Li metal electrodeposition in SPE-based cells is still lacking. In this study, we systematically assess the effect of cycling conditions on the CE of Li|SPE|Cu half cells and provide a thorough examination of different electrolyte chemistries, highlighting and explaining their performance across various parameters. While the efficiency of the PEO-based SPEs still falls short of the efficiency benchmark set by liquid and gel electrolytes, we demonstrated >95% CE with Lithium bis(fluorosulfonyl)imide (LiFSI)-based SPEs, surpassing previous reports for dry SPEs in a Li|SPE|Cu cells, this result marks a significant breakthrough. Furthermore, our findings highlight the critical impact of the Li-SPE interphase on these performance metrics. The LiFSI-based SPE forms a Li-rich, high-conductivity interphase, which not only enhances efficiency but also improves cycle life and Li deposit stability. These results underscore the importance of selecting the right polymer electrolyte chemistry and concentration to enhance SPE performance.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2024-11-20
DOI
https://doi.org/10.1021/acsami.4c15287
Citations
4
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.83

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article

Enhancing Efficiency, Stability, and Cycle Life of Lithium Metal Electrodeposition in Dry Solid-State Polymer Electrolytes

Netanel Shpigel, Daniel Sharon, Keren Shwartsman, Emily Ryan et al.
4 citations
ACS Applied Materials & Interfaces
Advanced Battery Materials and Technologies
0.83
article

Enhancing Efficiency, Stability, and Cycle Life of Lithium Metal Electrodeposition in Dry Solid-State Polymer Electrolytes

Netanel Shpigel, Daniel Sharon, Keren Shwartsman, Emily Ryan, Netta Bruchiel‐Spanier, Idan Bar-lev, Vivek Kumar Singh
article en
4 citations

Abstract

Dry solid polymer electrolytes (SPEs), particularly those based on poly(ethylene oxide) (PEO), hold significant potential for advancing solid-state Li-metal battery (LMB) technology. Despite extensive research over the years, a comprehensive evaluation of Coulombic efficiency (CE), deposit stability, and cycle life for reversible Li metal electrodeposition in SPE-based cells is still lacking. In this study, we systematically assess the effect of cycling conditions on the CE of Li|SPE|Cu half cells and provide a thorough examination of different electrolyte chemistries, highlighting and explaining their performance across various parameters. While the efficiency of the PEO-based SPEs still falls short of the efficiency benchmark set by liquid and gel electrolytes, we demonstrated >95% CE with Lithium bis(fluorosulfonyl)imide (LiFSI)-based SPEs, surpassing previous reports for dry SPEs in a Li|SPE|Cu cells, this result marks a significant breakthrough. Furthermore, our findings highlight the critical impact of the Li-SPE interphase on these performance metrics. The LiFSI-based SPE forms a Li-rich, high-conductivity interphase, which not only enhances efficiency but also improves cycle life and Li deposit stability. These results underscore the importance of selecting the right polymer electrolyte chemistry and concentration to enhance SPE performance.

ACS Applied Materials & InterfacesVol. 16(48)
Boston University (US), Hebrew University of Jerusalem (IL), Division of Materials Science and Engineering (AU), Ariel University (IL)
Division of Chemical, Bioengineering, Environmental, and Transport Systems, HORIZON EUROPE European Innovation Council
Responsible consumption and production
Openalex Percentile: Top 26%
Advanced Battery Materials and Technologies
0.83
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