普鲁士蓝
材料科学
阴极
电解质
溶解
钠
电池(电)
无机化学
钠离子电池
离子
氧化还原
容量损失
动力学
化学稳定性
快离子导体
锰
高分子
纳米技术
化学工程
电极
电化学
作者
Lina Ge,Yongpeng Cui,Yijun Song,Xiuli Gao,Xuejin Li,Pengyun Liu,Qingzhong Xue,Wei Xing
标识
DOI:10.1002/aenm.202500544
摘要
Abstract Mn‐based Prussian blue analogue (MnPBA) with high reaction potential and high reversible capacity is regarded as one of the most promising cathode materials for sodium ion batteries (SIBs). However, the catastrophic Mn dissolution leads to the collapse of the MnPBA structure and the rapid capacity decay. In this study, the Mn dissolution is effectively inhibited through a strong cross‐linking network between sodium alginate (SA) macromolecules and the Mn ions on the surface of MnPBA. The formed strong coordination bonding [Mn(SA) n ] firmly anchors Mn ions to avoid electrolyte attack, resulting in a nearly sixfold reduction in Mn dissolution. Moreover, this [Mn(SA) n ] cross‐linking network can accelerate the charge transfer, thereby improving the electrochemical reaction kinetics of sodium ions. Owing to this unique coordination model, the enhanced Mn‐SA electrodes exhibit a high discharge capacity (143.7 mAh g −1 ) and dramatic improvement in stability (over 1000 cycles). This study opens up a promising avenue for improving the structural stability of a wide range of Mn‐based cathode materials in practical battery systems.
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