Simultaneously Enhancing the Redox Potential and Stability of Multi-Redox Organic Catholytes by Incorporating Cyclopropenium Substituents

High redox potential, two-electron organic catholytes for nonaqueous redox flow batteries were developed by appending diaminocyclopropenium (DAC) substituents to phenazine and phenothiazine cores. The parent heterocycles exhibit two partially reversible oxidations at moderate potentials [both at lower than 0.7 V vs ferrocene/ferrocenium (Fc/Fc(+))]. The incorporation of DAC substituents has a dual effect on these systems. The DAC groups increase the redox potential of both couples by similar to 300 mV while simultaneously rendering the second oxidation (which occurs at 1.20 V vs Fc/Fc(+) in the phenothiazine derivative) reversible. The electron-withdrawing nature of the DAC unit is responsible for the increase in redox potential, while the DAC substituents stabilize oxidized forms of the molecules through resonance delocalization of charge and unpaired spin density. These new catholytes were deployed in two-electron redox flow batteries that exhibit voltages of up to 2.0 V and no detectable crossover over 250 cycles.

Automated summary

High redox potential, two-electron organic catholytes for nonaqueous redox flow batteries were developed by incorporating diaminocyclopropenium (DAC) substituents into phenazine and phenothiazine cores. The DAC groups increase the redox potential and render the second oxidation reversible, stabilizing the oxidized forms of the molecules through resonance delocalization of charge and unpaired spin density.