Tailoring MnO₂ Cathode Interface via Organic–Inorganic Hybridization Engineering for Ultra‐Stable Aqueous Zinc‐Ion Batteries

Abstract

Abstract Manganese (Mn)‐based aqueous zinc ion batteries show great promise for large‐scale energy storage due to their high capacity, environmental friendliness, and low cost. However, they suffer from the severe capacity decay associated with the dissolution of Mn from the cathode/electrolyte interface. In this study, theoretical modeling inspires that the amino acid molecule, isoleucine (Ile), can be an ideal surface coating material for α‐MnO 2 to stabilize the surface Mn lattice and mitigate Mn dissolution, thereby enhancing cycling stability. Furthermore, the coated Ile molecular layers can accumulate Zn 2+ ions from the electrolyte and promote those ions’ transport to the α‐MnO 2 cathode while prohibiting H 2 O from accessing the α‐MnO 2 surface, reducing the surface erosion. The compact organic–inorganic interface is experimentally synthesized for α‐MnO 2 utilizing Ile that shows homogeneous distribution on the well‐defined Ile‐α‐MnO 2 nanorod electrodes. The fabricated aqueous zinc‐ion battery exhibits a high specific capacity (332.8 mAh g −1 at 0.1 A g −1 ) and excellent cycling stability (85% after 2000 cycles at 1 A g −1 ) as well as good inhibition toward Mn 2+ dissolution, surpassing most reported cathode materials. This organic–inorganic hybrid interface design provides a new, simple avenue for developing high‐performance and low‐cost Mn‐based aqueous zinc ion batteries (AZIBs).