Abstract

Radical anions of electrochemically reduced compounds (anolytes) have been suggested for storage of negative charge in nonaqueous redox flow batteries. The lower the redox potential of the anolyte molecule, the higher is the stored energy density. However, the stability of the radical ions frequently suffers as their redox potentials become extreme, and there is a compromise between the energy density and the chemical stability in the active form. In this study, we scrutinize this trade-off using one such “extreme,” the heterocyclic anolyte 2,1,3-benzothiadiazole, BzNSN, by adjusting the redox potential of BzNSN via installed electron-donating and electron-withdrawing groups. We show that the stability of the radical anion strongly depends on the degree of ion pairing in solution, with the worst being for the contact lithium ion pairs. For BzNSN derivatives, there is a strong correlation between the lifetime of the radical anion and the redox potential. The root cause appears to be the proton transfer fro...

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