A1 Refereed original research article in a scientific journal

Electrochemical Performance of a New Triazole Functionalized Ferrocene in Aqueous Redox Flow Batteries




AuthorsEken, Taha Yasin; Gonzalez, Gabriel; Peljo, Pekka; Koz, Gamze

PublisherWILEY

Publishing placeHOBOKEN

Publication year2025

JournalApplied Organometallic Chemistry

Journal name in sourceAPPLIED ORGANOMETALLIC CHEMISTRY

Journal acronymAPPL ORGANOMET CHEM

Article numbere7820

Volume39

Issue2

Number of pages7

ISSN0268-2605

eISSN1099-0739

DOIhttps://doi.org/10.1002/aoc.7820

Web address https://doi.org/10.1002/aoc.7820

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/458589461


Abstract
A new 1,2,3-triazole functionalized ferrocene (1,2,3-TAFc) produced by Cu(I)-catalyzed click reaction was investigated as positive electrolyte for aqueous organic flow batteries (AOFBs). The molecule is highly soluble in 1 M hydrochloric acid and displays high electrochemical reversibility. 1,2,3-TAFc demonstrated good stability during cycling with a low capacity decay (0.011%/cyc, 3.0%/day) and high Coulombic efficiency (99.4%) over 280 cycles when tested in a flow battery at low concentration. This low capacity decay was attributed to the instability of ferrocene. These findings indicate that a stable and water-soluble catholyte for AOFBs can be obtained with structural modifications of 1,2,3-TAFc.A new type of ferrocene catholyte for AOFBs based on a 1,2,3-triazole moiety was introduced. 1,2,3-TAFc was prepared easily via click chemistry with a one-pot, two steps reaction sequence with 73% overall yield. The CV and flow battery experiments demonstrated the reversible and stable nature of the material. The cycling battery tests show a high stability of 1,2,3-TAFc in acidic electrolyte with low capacity decay (0.011%/cyc) and high Coulombic efficiency (99.4%).image

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Funding information in the publication
We are grateful to the Bursa Technical University Scientific Research Fund (Project No. 231N002) for financial support. G. G. gratefully acknowledges the financial support from the University of Turku Graduate School. P. P. gratefully acknowledges the financial support from European Research Council Starting Grant (agreement no. 950038). This work partly utilized the Materials Research Infrastructure (MARI) at the University of Turku.


Last updated on 2025-27-03 at 13:10