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Demonstrates enhanced capacity retention in manganese oxide cathodes, suggesting a novel engineering approach for aqueous batteries.
Manganese oxide cathodes are promising candidates for aqueous batteries owing to their high operating voltage and large capacity. However, they suffer from severe Mn3+ disproportionation and Mn2+ dissolution in acidic aqueous batteries, hindering their practical applications. Herein, we construct an in situ trifunctional (conductive, hydrophobic, self-adaptive) interphase using PDMS-DE@PANI (epoxypropoxypropyl-terminated polydimethylsiloxane@polyaniline) core–shell nanocapsules for encapsulating Mn2O3. The electrochemically driven release of the liquid PDMS-DE core, synergizing with the PANI shell, effectively suppresses Mn2+ dissolution while ensuring rapid electron/ion transfer. Consequently, the PD-Mn2O3 cathode delivers a record-high capacity of 340 mAh g–1 at 0.2 A g–1 and retains 201 mAh g–1 (92% capacity retention) after 800 cycles at 1 A g–1. Paired with a HATN anode, the full proton battery achieves an exceptional energy density of 140 Wh kg–1 with 80% capacity retention over 800 cycles. This dynamic interphase engineering provides a robust strategy for developing high-energy, ultrastable aqueous proton batteries.
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Zhou et al. (2026) studied this question.
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