DFT calculation, a practical tool to predict the electrochemical behaviour of organic electrolytes in aqueous redox flow batteries

Herein, a computational predictive tool for redox flow batteries based on NBO and ADCH charge distribution studies is presented and supported by experimental evidence. Using highly water soluble (>2 M) non-planar 2,2′-bipyridinium salts as a case of study, this work presents a DFT protocol that successfully predicts the stability and forecasts their potential application as active materials for Aqueous Organic Redox Flow Batteries (AORFB). An initial theoretical-experimental characterization of selected bipyridines served to determine the effect of the ring size, geometry, and electron density on the physico-chemical properties of the materials. Nonetheless, the NBO and ADCH charge analyses were essential tools to understand the stability of the reduced species in terms of electronic delocalization and the importance of the molecular design on the stability of electrolyte for AORFB. Based on these results, the cell performance of seven-membered 2,2′-bypiridinium salt, (2), and m-Me substituted homologous, (4), were compared. The significantly lower capacity decay rendered by compound 4 based electrolyte, (0.35%/cycle) compared with compound 2 based electrolyte, (0.71%/cycle) was in good agreement with the predicted stability. The aim of this work is to highlight the powerful synergy between DFT calculations and organic chemistry in predicting the behaviour of different negolytes.