Skip to main navigation Skip to search Skip to main content

Lithium Ferrocyanide Catholyte for High-Energy and Low-cost Aqueous Redox Flow Batteries**

  • School of Chemistry and Chemical Engineering, Harbin Institute of Technology
  • Harbin Institute of Technology
  • National University of Singapore

Research output: Contribution to journalArticlepeer-review

Abstract

Aqueous redox flow batteries (ARFBs) are a promising technology for grid-scale energy storage, however, their commercial success relies on redox-active materials (RAM) with high electron storage capacity and cost competitiveness. Herein, a redox-active material lithium ferrocyanide (Li4[Fe(CN)6]) is designed. Li+ ions not only greatly boost the solubility of [Fe(CN)6]4− to 2.32 M at room temperature due to weak intermolecular interactions, but also improves the electrochemical performance of [Fe(CN)6]4−/3−. By coupling with Zn, ZIRFBs were built, and the capacity of the batteries was as high as 61.64 Ah L−1 (pH-neutral) and 56.28 Ah L−1 (alkaline) at a [Fe(CN)6]4− concentration of 2.30 M and 2.10 M. These represent unprecedentedly high [Fe(CN)6]4− concentrations and battery energy densities reported to date. Moreover, benefiting from the low cost of Li4[Fe(CN)6], the overall chemical cost of alkaline ZIRFB is as low as $11 per kWh, which is one-twentieth that of the state-of-the-art VFB ($211.54 per kWh). This work breaks through the limitations of traditional electrolyte composition optimization and will strongly promote the development of economical [Fe(CN)6]4−/3−-based RFBs in the future.

Original languageEnglish
Article numbere202304667
JournalAngewandte Chemie - International Edition
Volume62
Issue number25
DOIs
StatePublished - 19 Jun 2023
Externally publishedYes

Keywords

  • Aqueous Redox Flow Battery
  • Capacity
  • Li[Fe(CN)]
  • Low-Cost
  • Solubility

Fingerprint

Dive into the research topics of 'Lithium Ferrocyanide Catholyte for High-Energy and Low-cost Aqueous Redox Flow Batteries**'. Together they form a unique fingerprint.

Cite this