Vitrimer with dynamic imine bonds as a solid-state electrolyte for lithium metal batteries
- Authors
- Yang, Seonghyeon; Park, Seungjin; Kim, Seongseop; Kim, Sung-Kon
- Issue Date
- Oct-2024
- Publisher
- Elsevier
- Keywords
- Lithium metal battery; Solid polymer electrolyte; Dynamic bond; Covalent adaptable networks; Interface
- Citation
- Materials Today Energy, v.45, pp 1 - 8
- Pages
- 8
- Indexed
- SCIE
SCOPUS
- Journal Title
- Materials Today Energy
- Volume
- 45
- Start Page
- 1
- End Page
- 8
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/26385
- DOI
- 10.1016/j.mtener.2024.101690
- ISSN
- 2468-6069
2468-6069
- Abstract
- In this study, vitrimer solid polymer electrolytes (V-SPEs) with dynamic imine bonds are synthesized for use in lithium metal batteries (LMBs). The optimal composition of V-SPEs is investigated by changing the ratio of ethylene oxide (EO) to lithium-ion and the length of the EO units. V-SPEs with longer EO segments exhibit high ionic conductivity of up to 3.25 x 10(-4) S/cm at 60 degrees C. The stress relaxation behavior of the V-SPE demonstrates a gradual decrease in viscosity following the Arrhenius law and an activation energy of 52 kJ/mol, attributed to the dynamic exchange reaction. Furthermore, the imine exchange reaction endows self-healing capability to V-SPEs at ambient temperature. Note that the reduction in initial interfacial resistance over 40 charge-discharge cycles indicates enhanced compatibility between the electrode and electrolyte due to the dynamic exchange reaction. The LMB full cell having V-SPE shows a large initial discharge capacity of 154.7 mAh/g, good C-rate capability, and long cycle lives for at least 100 charge-discharge cycles at 60 degrees C and 0.1 C. This suggests that V-SPEs hold a great potential as solid electrolytes for LMBs. (c) 2024 Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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Collections - College of Engineering > Department of Chemical and Biochemical Engineering > 1. Journal Articles

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