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Transport number determination and relevance for lithium metal batteries using localized highly concentrated electrolytes
ID Ishfaq, Hafiz Ahmad (Author), ID Cruz Cardona, Carolina (Author), ID Tchernychova, Elena (Author), ID Johansson, Patrik (Author), ID Gaberšček, Miran (Author), ID Dominko, Robert (Author), ID Drvarič Talian, Sara (Author)

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Abstract
The lithium transport number (t$_{Li^+}$) determination of fluorinated ether (1,2-(1,1,2,2-tetrafluoroethoxy) ethane, TFEE)-based localized highly concentrated electrolytes (LHCEs) with 1,2-dioxolane (DOL) and dimethoxyethane (DME) as solvents has been explored using molecular dynamics simulations, nuclear magnetic resonance spectroscopy, Bruce-Vincent’s method, and low-frequency electrochemical impedance spectroscopy (EIS). We showcase that the TFEE-DOL LHCE has a t$_{Li^+}$ as high as 0.65 but, on the other hand, exhibits low Coulombic efficiency (<90%) and poor stability vs Li metal anodes, i.e., in a lithium metal battery (LMB) setting. In contrast, the TFEE-DME LHCE shows high Coulombic efficiency (98.9%) and stability, despite a much lower t$_{Li^+}$ (0.25). A significant migration resistance through the porous solid electrolyte interphase (SEI) for the former is the likely explanation, as revealed by EIS and assisted by scanning electron microscopy and X-ray photoelectron spectroscopy experiments. We thus find the interfacial properties at the Li metal anode to be more crucial than the ionic transport through the bulk of the electrolyte for LMB performance. We therefore propose that the focus should be put on the full (operando) impedance spectra of Li metal anodes in contact with electrolytes, since it enables the characterization of the interphase layer(s), rather than solely determining the (bulk) t$_{Li^+}$ of the electrolytes.

Language:English
Keywords:electrodes, electrolytes, ions, metals, surface chemistry
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Publication status:Published
Publication version:Version of Record
Year:2025
Number of pages:Str. 2485–2495
Numbering:Vol. 37, iss. 7
PID:20.500.12556/RUL-168456 This link opens in a new window
UDC:544.5/.6
ISSN on article:1520-5002
DOI:10.1021/acs.chemmater.4c03067 This link opens in a new window
COBISS.SI-ID:231531523 This link opens in a new window
Publication date in RUL:14.04.2025
Views:755
Downloads:284
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Record is a part of a journal

Title:Chemistry of materials
Shortened title:Chem. mater.
Publisher:American Chemical Society
ISSN:1520-5002
COBISS.SI-ID:17044263 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:elektrokemija, litij, NMR, spektroskopija, elektroliti, SEI

Projects

Funder:EC - European Commission
Funding programme:H2020
Project number:945357
Name:Doctorate Programme on Emerging Battery Storage Technologies INspiring Young scientists
Acronym:DESTINY

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P2-0423
Name:Sodobni akumulatorji kot podpora zelenemu prehodu in elektromobilnosti

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:Z2-4465
Name:Raziskava reakcijskih in transportnih mehanizmov za kovinsko magnezijevo akumulatorsko anodo

Funder:VINNOVA
Project number:2019-00064

Funder:BASE - Batteries Sweden

Funder:Swedish Research Council
Project number:2021-00613

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