化学
锰
插层(化学)
电化学
阴极
无机化学
锌
水溶液
兴奋剂
化学工程
双金属片
电极
材料科学
催化作用
有机化学
光电子学
物理化学
工程类
作者
Jing Zeng,Zhihao Zhang,Yong Chen,Xiaobin Chen,Hanbing He,Jiexi Wang
标识
DOI:10.1016/j.jelechem.2023.117306
摘要
Manganese dioxide with high operating voltage and satisfactory energy density have been identified as the promising cathode materials for aqueous zinc-ion batteries (AZIBs). However, the structural instability of manganese-based materials during the (dis)charging process limits their further development. Herein, sodium-potassium co-doped layered K0.37Na0.18MnO2·xH2O (KNMOH) are synthesized by a liquid-phase synthesis method at room temperature. The co-doping of Na+ and K+ stabilizes the layered structure, widens the layer spacing and has the effect of electrostatic shielding to facilitate the (de)intercalation of Zn2+. Benefiting from the stable structure and nanoscale size, the flower-like KNMOH cathode maintained a high specific capacity of 239.1 mAh·g−1 after 700 cycles at 500 mA·g−1. Simultaneously, this work firstly reveals that the presence of K8(SO4)(SO3OH)6 suppressed the generation of Zn4SO4(OH)6·0.5H2O, resulting in more free Zn2+ and high reversibility. This co-doped design of bimetallic ions insertion enhances the electrochemical performance and provides a new idea for the improvement of the manganese-based cathode materials for AZIBs.
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