Redox flow batteries (RFBs) have emerged as significant energy storage systems amid the growing adoption of renewable energy. However, the advancement of all-organic RFBs is hindered by material crossover, limited energy density, and the time-consuming selection of suitable electrolyte partners. To address these challenges, bipolar redox-active organic molecules (BRMs) show promise for charge storage in symmetric organic redox flow batteries (SORFBs), although their development can be complex and tedious. In this study, we report an approach aimed at streamlining the identification of suitable compounds through an examination of the organophotocatalyst literature, illustrated through six acridinium compounds exhibiting stable redox states. These compounds were thoroughly characterized in electrochemical cells and subjected to cycling tests in fully symmetric flow batteries. Notably, a trisubstituted electron-rich acridinium compound emerged as a potential candidate, demonstrating over 20 days of cycling stability. Given the extensive library of organic catalysts and the advantages of SORFB designs, this approach will prove to be essential for developing an innovative electrochemical storage system.
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Too Much of a Good Thing? Assessing Performance Tradeoffs of Two-Electron Compounds for Redox Flow Batteries
Engineering redox-active compounds to support stable multi-electron transfer is an emerging strategy for enhancing the energy density and reducing the cost of redox flow batteries (RFBs). However, when sequential electron transfers occur at disparate redox potentials, increases in electrolyte capacity are accompanied by decreases in voltaic efficiency, restricting the viable design space. To understand these performance tradeoffs for two-electron compounds specifically, we apply theoretical models to investigate the influence of the electron transfer mechanism and redox-active species properties on galvanostatic processes. First, we model chronopotentiometry at a planar electrode to understand how the electrochemical response and associated concentration distributions depend on thermodynamic and mass transport factors. Second, using a zero-dimensional galvanostatic charge/discharge model, we assess the effects of these key descriptors on performance (i.e., electrode polarization and voltaic efficiency) for a single half-cell. Finally, we extend the galvanostatic model to include two-electron compounds in both half-cells, demonstrating compounding voltage losses for a full cell. These results fundamentally show why multi-electron compounds with disparate redox potentials are less attractive than those with concerted electron transfer. As such, we suggest new directions for molecular and systems engineering to improve the prospects of these materials for RFBs.
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- Award ID(s):
- 1805566
- PAR ID:
- 10336178
- Date Published:
- Journal Name:
- Journal of The Electrochemical Society
- Volume:
- 168
- Issue:
- 5
- ISSN:
- 0013-4651
- Page Range / eLocation ID:
- 050501
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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