“…The development of Na-ion alluaudite cathodes has been hindered by the limited number of electrochemically active M species in this structure type. Barring just a few compositions, ,, only Fe 2+ /Fe 3+ redox has been harnessed, even in compounds containing multiple M species. ,,− For instance, Na 2 Fe 3– x Mn x (PO 4 ) 3 alluaudites can reach up to 140 mAh/g of reversible capacity for the x = 0 end-member, and a steady decrease in capacity is observed as x increases. ,,, These cathodes operate at 2.7 V vs Na/Na + , and no capacity can be attributed to the higher potential Mn 2+ /Mn 3+ couple, leading to rather low energy densities. In contrast, sulfate alluaudites exhibit unprecedently high operating voltages, so much so that the potentials of Ni- and Co-based systems fall outside of the electrochemical stability window of typical electrolytes. , The combination of a highly unstable structure on Na extraction (due to strong repulsion between edge-sharing MO 6 octahedra in the oxidized state) and a less negative “–2” charge on the sulfate group compared to the phosphate group results in low capacities for sulfate alluaudites. ,, Overall, a better understanding of the origin of the electrochemical inertness of Mn, with a redox potential well below the decomposition potential of organic electrolytes even in a sulfate alluaudite, is warranted, and the design of “beyond Fe” alluaudite cathodes is desirable.…”