Abstract Iron-ion batteries represent a compelling energy storage solution due to the cost-effectiveness, suitable redox potential, and high capacity of Fe negative electrodes. Polyaniline positive electrodes for iron-ion batteries have demonstrated promising electrochemical redox properties, but face limited redox-accessible groups and unstable −NH− sites. Here we show phosphorus redox activity in a carboxyl small molecule electrode. 4,4′,4″-phosphanetriyltribenzoic acid and 4,4′,4″-nitrilotribenzoic acid are designed via modulating the electron-donating P and tert-N motifs, showing tuned charge distributions and energy levels. With the decrease of the electronegativity and energy barrier (N > P), 4,4′,4″-phosphanetriyltribenzoic acid exhibits stronger Fe 2+ coordination with carboxyl sites, and brings closed CF 3 SO 3 − proximity to P centers. This feature ensures high activity of carboxyl/phosphorus sites with low activation energy (0.24 vs . 0.29 eV for 4,4′,4″-nitrilotribenzoic acid). 4,4′,4″-phosphanetriyltribenzoic acid with P-extended conjugated structure achieves low energy gap (2.28 eV) compared to its individual carboxyl or P-containing counterparts (2.71/3.16 eV), thereby enabling high utilization of carboxyl/P motifs (98.5%) and enhanced redox voltage (0.8 V). A stable 4 e − Fe 2+ /CF 3 SO 3 − storage of 4,4′,4″-phosphanetriyltribenzoic acid positive electrode endows Fe battery with high specific capacity (276 mAh g −1 ) and cycling stability (60,000 cycles). This work highlights the potential of phosphorus-active organic materials toward iron-ion batteries.
Zhang et al. (Sun,) studied this question.