Aqueous organic redox flowb atteries (AORFBs) are ap romising electrochemical technology for large-scale energy storage.W er eport ab iomimetic,u ltra-stable AORFB utilizing an amino acid functionalizedp henazine (AFP). A series of AFPs with various commercial amino acids at different substituted positions were synthesized and studied. 1,6-AFPs displaym uchh igher stability during cycling when compared to 2,7-and 1,8-AFPs.M echanism investigations reveal that the reduced 2,7-and 1,8-AFPs tend to tautomerize and lose their reversible redox activities,w hile 1,6-AFPs possess ultra-high stability both in their oxidized and reduced states.B yp airing 3,3'-(phenazine-1,6-diylbis(azanediyl))dipropionic acid (1,6-DPAP)w ith ferrocyanide at pH 8w ith 1.0 Melectron concentration, this flowbattery exhibits an OCV of 1.15 Vand an extremely lowcapacity fade rate of 0.5 %per year.These results show the importance of molecular engineering of redox-active organics for robust redox-flowb atteries.