Elucidating the Iron-Based Ionic Liquid [C4py][FeCl4]: Structural Insights and Potential for Nonaqueous Redox Flow Batteries

Balischewski, Christian;Bhattacharyya, Biswajit;Bailey, Josh J.;Place, Scott D.;Taubert, Andreas;et.al.
(2024) Advanced Functional Materials — Vol. 34, n° 12, p. 2311571 (2024)

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Authors
  • Balischewski, Christian
    Author
  • Bhattacharyya, Biswajit
    Author
  • Bailey, Josh J.
    Author
  • Place, Scott D.
    Author
  • Li, WeiyangUCLouvain
    Author
  • Garcia, Yannorcid-logoUCLouvain
    Author
  • Taubert, Andreasorcid-logo
    Author
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Abstract
In this study, a low-melting organic-inorganic crystalline ionic liquid compound, N-butyl pyridinium tetrachlorido ferrate (III) is described. The material can easily be synthesized using a one-pot approach in an ionic liquid medium. Single-crystal X-ray diffraction confirms that the basic inorganic block is [FeCl4]−, which is counterbalanced by an N-butyl pyridinium cation. The compound exhibits a melting point of 37.6 °C by differential scanning calorimetry, which is among the lowest values for a pyridinium-based metal-containing ionic liquid. The material shows promising electrochemical behavior at room temperature in both aqueous and nonaqueous solvents, and at elevated temperatures in its pure liquid state. Given its appreciable solubility in both water and acetonitrile, the compound can act as a redox-active species in a supporting electrolyte for redox flow battery applications. These classes of low-melting ionic solids with long-range order and interesting electrochemical applications are potential candidates for a range of green energy storage and harvesting systems.
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Citations

Balischewski, C., Bhattacharyya, B., Bailey, J. J., Place, S. D., Nockemann, P., Kim, J., Wedel, A., Gahlaut, S., Bald, I., Li, W., Garcia, Y., Sperlich, E., Günter, C., Kelling, A., & Taubert, A. (2024). Elucidating the Iron-Based Ionic Liquid [C4py][FeCl4]: Structural Insights and Potential for Nonaqueous Redox Flow Batteries. Advanced Functional Materials, 34(12), 2311571. https://doi.org/10.1002/adfm.202311571 (Original work published 2024)