Flow Battery Molecular Reactant Stability Determined by Symmetric Cell Cycling Methods
By M. Goulet, M. Aziz. 2018
175 citations recorded by the source corpus.
We present an unbalanced compositionally-symmetric flow cell method for revealing and quantifying different mechanisms for capacity fade in redox flow batteries that are based on molecular energy storage. We utilize it, accompanied in some cases by a corresponding static-cell cycling method, to study capacity fade in cells comprising anthraquinone di-sulfonate, di-hydroxy anthraquinone, iron hexacyanide, methyl viologen, and bis-trimethylammoniopropyl viologen. In all cases the cycling capacity decay is reasonably consistent with exponential in time and is independent of the number of charge-discharge cycles imposed. By introducing pauses at various states of charge of the capacity-limiting side during cycling, we show that in some cases the temporal fade time constant is dependent on the state of charge. These observations suggest that molecular lifetime is dominated by chemical rather than electrochemical mechanisms. These mechanisms include irrecoverable chemical decomposition and recoverable interactions with cell materials. We conclude with recommendations for cell cycling protocols for evaluating stability of single electrolytes.
Subfields: Automotive Engineering, Electrical and Electronic Engineering
View Paper: https://www.semanticscholar.org/paper/ebe9b8d5a2e8adb9f7b19c304864cc473d2a0d5d
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In Electrical and Electronic Engineering
Citations in the corpus
- Alkaline Quinone Flow Battery with Long Lifetime at pH 12 (2018, background): “The symmetric cell configuration, in which the two sides have the same electrolyte composition, is a simple and direct probe of chemical and electrochemical stability of RFB reactants and is described in full in a separate report.(16) Any observed capacity fade is directly related to deactivation of”