Manganese oxides are promising host materials in rechargeable aqueous batteries due to their low cost and high capacity; however, their practical applications have long been restricted by their sluggish reaction kinetics and poor cycling stability. Herein, the layered KHMnO·0.28HO (K36) with a proton and Zn cointercalation mechanism leads to a progressive phase evolution from layer-type K36 to hybrid layer-type KHZnMnO·HO and spinel-type ZnMnO nanocrystal after a long-term cycle. Accordingly, K36 shows a high specific capacity (∼329.8 mAh g at 0.1C), a superior rate performance (∼100.1 mAh g at 10C), and a remarkable cycling stability (capacity retention of ∼93.4% over 3000 cycles at 4C). This work provides a new viewpoint of enhancing electrode performance via generating hybrid phases under electrochemical driving and will be a benefit to developing the next-generation aqueous batteries.
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http://dx.doi.org/10.1021/acsami.1c03671 | DOI Listing |
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