Aqueous reversible zinc batteries using near-neutral aqueous electrolytes like ZnSO₄/H₂O are the cheaper, safer and more durable alternatives to typical nonaqueous Li-ion batteries, and seem more suited for renewable and large-scale energy storage. Yet their advancement is hindered by a limited choice of positive host materials due to sluggish solid-state diffusion of divalent zinc ions inside most inorganic structures. Much work has focused on layered and tunneled transition metal oxides with large interstitial sites or open interlayer galleries for high capacity and high rate Zn²⁺ storage. While these oxides deliver attractive electrochemical performance, formation/disappearance of an insulating side product - Zn₄SO₄(OH)₆·nH₂O – during battery discharge/charge has been noted for many of them. The insulating byproduct may not only be detrimental to power capability and extended cycling, its origin has been linked to parasitic side reactions involving metal dissolution and consequent increase of the electrolyte pH. An unequivocal understanding of its reversible appearance is missing, however. This presentation will delve into this topic, conveying a comprehensive mechanism that leads to the hydroxysulfate (Zn₄SO₄(OH)₆·nH₂O) formation/decomposition during zinc battery cycling, and demonstrate strategies to inhibit it. In addition, this presentation will cover our work on novel organic hosts, which owing to their malleable crystal structure provide facile and reversible Zn²⁺ storage. Operando X-ray diffraction, electron microscopy, and impedance analysis have been applied together with theoretical calculations to elucidate the Zn²⁺ storage mechanism. The deeper understanding gained has been channeled to tune the cathode design towards stable electrochemical cycling