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Organic small-molecules with redox activity are promising cathode candidates for aqueous zinc-ion batteries (AZIBs) due to their low cost, high safety and high theoretical capacity. However, their severe dissolution leads to unsatisfactory electrochemical performance. Here, a dihydro-octaaza-pentacene (DOP) compound is synthesized as a cathode for AZIBs by extending its N heterocyclic molecular structure. The extended N heterocyclic structure provides dual active sites of n-type (C═N) and p-type (−NH−) redox reactions while reducing dissolution through enhanced π-conjugation. Hence, the Zn//DOP battery demonstrates improved performance, e.g., an enhanced capacity of 360 mAh g –1 at 0.05 A g –1 . Even under extended temperature conditions of – 50 and 50 °C, the batteries still maintain the capacities of 172 and 312 mAh g –1, respectively. In/ ex-situ spectroscopy provide a thorough understanding of the storage mechanisms of cations and anions (Zn 2+ /H + and ClO 4 – ) through multielectron transfer process occurring at dual electroactive sites. This strategy offers a promising approach to designing high-performance zinc-organic batteries for sustainable energy storage.
Kang et al. (Thu,) studied this question.