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Shows improved energy storage in aqueous redox flow batteries, suggesting enhanced capacity and stability.
A growing share of variable renewable generation requires low‐cost, long‐duration grid‐level energy storage. Aqueous organic redox flow batteries (AORFBs) offer tunable molecular chemistry and scalable flow architecture; acidic systems enable high power and leverage mature vanadium‐flow hardware. A central challenge is designing posolytes that combine high redox potential, solubility, capacity density, and stability. Here, we report a two‐electron azo‐based zwitterionic molecule 4,4′‐azo‐bis(1‐pyridinium‐3‐propane‐sulfonate) (ABPS) that addresses these constraints through intrinsic structural features. The zwitterionic character dramatically enhances water solubility (1.30 M in 2.0 M H 2 SO 4 ) while maintaining overall electroneutrality, thereby intrinsically reducing molecule crossover and suppressing capacity decay during cycling. Symmetric cell testing confirms outstanding stability over 3800 cycles (∼100 days) with an average coulombic efficiency (CE) of 99.98% and nearly zero capacity loss (0.198% year −1 ). In the full cell demonstration, ABPS delivers a high voltage of 1.14 V (paired with V 2+/3+ ). A capacity density of 48.5 Ah L −1 and the corresponding posolyte energy density of 55.3 Wh L −1 are achieved (1.0 M molecule concentration), and an ultralow capacity decay rate of 0.084% year −1 over 1100 h of operation. The rational design of azo‐based zwitterionic structure thus offers a promising universal route to durable, high‐power acidic AORFB posolytes.
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Wang et al. (2026) studied this question.
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