Zhao Yi, Zhou Rongkun, Song Zhihang, Zhang Xiaodong, Zhang Tao, Zhou Anbin, Wu Feng, Chen Renjie, Li Li
Beijing Key Laboratory of Environmental Science and Engineering, School of Materials Science and Engineering, Beijing Institute of Technology, Beijing, 100081, China.
Advanced Technology Research Institute, Beijing Institute of Technology, Jinan, 250300, China.
Angew Chem Int Ed Engl. 2022 Dec 5;61(49):e202212231. doi: 10.1002/anie.202212231. Epub 2022 Nov 10.
Due to the excellent specific capacity and high working voltage, manganese oxide (MnO ) has attracted considerable attention for aqueous zinc-ion batteries (AZIBs). However, the irreversible structural collapse and sluggish ionic diffusion lead to poor rate capability and inferior lifespan. Herein, we proposed a novel organic/inorganic hybrid cathode of carbon-based poly(4,4'-oxybisbenzenamine)/MnO (denoted as C@PODA/MnO ) for AZIBs. Various in/ex situ analyses and theoretical calculations prove that PODA chains with C=N groups can provide a more active surface/interface for ion/electron mobility and zinc ion storage in the hybrid cathode. More importantly, newly formed Mn-N interfacial bonds can effectively promote ion diffusion and prevent Mn atoms dissolution, enhancing redox kinetics and structural integrity of MnO . Accordingly, C@PODA/MnO cathode exhibits high capacity (321 mAh g or 1.7 mAh cm at 0.1 A g ), superior rate performance (88 mAh g at 10 A g ) and excellent cycling stability over 2000 cycles. Hence, rational interfacial designs shed light on the development of organic/inorganic cathodes for advanced AZIBs.
由于具有出色的比容量和高工作电压,氧化锰(MnO )在水系锌离子电池(AZIBs)领域引起了广泛关注。然而,不可逆的结构坍塌和缓慢的离子扩散导致其倍率性能较差且寿命较短。在此,我们提出了一种用于AZIBs的新型有机/无机混合正极——碳基聚(4,4'-氧联二苯胺)/MnO (记作C@PODA/MnO )。各种原位/非原位分析和理论计算表明,带有C=N基团的PODA链可为混合正极中的离子/电子迁移以及锌离子存储提供更活跃的表面/界面。更重要的是,新形成的Mn-N界面键可有效促进离子扩散并防止Mn原子溶解,增强MnO 的氧化还原动力学和结构完整性。因此,C@PODA/MnO 正极在0.1 A g 时展现出高容量(321 mAh g 或1.7 mAh cm )、优异的倍率性能(在10 A g 时为88 mAh g )以及超过2000次循环的出色循环稳定性。因此,合理的界面设计为先进AZIBs的有机/无机正极开发提供了思路。