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Hydrophobic Deep Eutectic Solvent (DES) Design Enables Optimally Hydrated DES-in-Water Electrolytes for High-Performance Bromine Redox-Enhanced Energy Storage Systems

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Abstract
Supercapacitors are renowned for rapid charging, high power density, and long lifespan, yet their practical applications are limited by low energy densities. Redox-enhanced electrochemical capacitors (redox ECs) address this limitation by incorporating redox-active electrolytes, enabling Faradaic charge storage. Bromide is a promising catholyte due to its high reduction potential, excellent solubility, and low cost. However, the generation of corrosive Br2 and the cross-diffusion of soluble polybromides result in suboptimal cell efficiency including severe self-discharge and reduced cycle life. Although solid complexing agents have been used to suppress polybromides' cross-diffusion, this approach necessitates water, which inherently limits electrochemical and thermal stability. Here, a hydrated deep eutectic solvent (HDES) electrolyte is developed by combining tetrabutylammonium bromide (TBAB) with ethylene glycol. This HDES system effectively utilizes the multifunctional roles of TBAB: the bromide anion functions as a catholyte, while the TBA cation suppresses polybromides' cross-diffusion as a built-in solid complexing agent. Critically, unlike previous studies that focus on minimally hydrated DESs, this system leverages the hydrophobic effect of TBAB to accommodate higher water content, addressing challenges inherent to DESs while maintaining superior electrochemical and thermal stability. The optimized HDES-50 electrolyte, containing 50 wt.% water, provides a robust and efficient solution for advanced redox ECs. © 2025 The Author(s). Advanced Functional Materials published by Wiley-VCH GmbH.
Author(s)
Eom, Tae PyeongLee, GunwooCho, Young HunLim, YounjeeYoo, Seung Joon
Issued Date
2025-03
Type
Article
DOI
10.1002/adfm.202424243
URI
https://scholar.gist.ac.kr/handle/local/8996
Publisher
John Wiley and Sons Inc
Citation
Advanced Functional Materials
ISSN
1616-301X
Appears in Collections:
Department of Materials Science and Engineering > 1. Journal Articles
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