阳极
阴极
材料科学
沸石咪唑盐骨架
纳米孔
电解质
化学工程
电化学
双金属片
水溶液
法拉第效率
储能
复合数
纳米技术
电化学窗口
钾离子电池
兴奋剂
电池(电)
咪唑酯
纳米棒
容量损失
枝晶(数学)
碳纤维
离子电导率
无机化学
导电体
作者
Rui Zhang,X W Zhang,Jialiang Li,Wenhua Li,Huan Pang
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2026-04-26
卷期号:31 (9): 1429-1429
标识
DOI:10.3390/molecules31091429
摘要
Manganese-based cathodes offer high capacity, low cost, and safety for aqueous zinc-ion batteries (AZIBs), yet suffer from Mn dissolution, Jahn–Teller distortion, and sluggish Zn2+ kinetics. Herein, a Zn/Co co-doped MnO nanoporous carbon composite (denoted as ZnCo-MnO@NPC) derived from a bimetallic ZnCoMn metal–organic framework (ZnCoMn-MOF-74) is successfully synthesized and proposed as a high-performance cathode to address these challenges. The introduction of Zn2+ increases the initial specific capacity of MnO, while Co doping effectively suppresses the Jahn–Teller distortion and improves the integrity of the structure. Furthermore, the nanoporous carbon matrix facilitates electrolyte infiltration and accelerates ionic transport. To further suppress dendrite growth and enhance cycling stability, a zeolitic imidazolate framework (ZIF-8) protective layer is engineered on the zinc anode (denoted as ZIF-8@Zn), effectively mitigating dendrite formation. The ZnCo-MnO@NPC//ZIF-8@Zn full cell demonstrates superior electrochemical performance, delivering 281.3 mAh g−1 at 0.1 A g−1 and retaining 98.7% of this value after 3500 long-term cycles at 2.0 A g−1, a remarkable finding that underscores its potential for high-performance energy storage. Collectively, this work highlights that transition metal ion doping represents an effective way to design efficient high-performance MOF-derived cathodes of AZIBs.
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