Yan Lei, Zhang Yu, Ni Zhigang, Zhang Yong, Xu Jie, Kong Taoyi, Huang Jianhang, Li Wei, Ma Jing, Wang Yonggang
Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Institute of New Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Fudan University, Shanghai 200433, China.
Key Laboratory of Mesoscopic Chemistry of MOE School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, Jiangsu 210023, China.
J Am Chem Soc. 2021 Sep 22;143(37):15369-15377. doi: 10.1021/jacs.1c06936. Epub 2021 Sep 7.
Zn-organic batteries are attracting extensive attention, but their energy density is limited by the low capacity (<400 mAh g) and potential (<1 V vs Zn/Zn) of organic cathodes. Herein, we propose a long-life and high-rate Zn-organic battery that includes a poly(1,5-naphthalenediamine) cathode and a Zn anode in an alkaline electrolyte, where the cathode reaction is based on the coordination reaction between K and the C═N group (i.e., C═N/C-N-K conversion). Interestingly, we find that the discharged Zn-organic battery can recover to its initial state quickly with the presence of O, and the theoretical calculation demonstrates that the K-N bond in the discharged cathode can be easily broken by O via redox reaction. Accordingly, we design a chemically self-charging aqueous Zn-organic battery. Benefiting from the excellent self-rechargeability, the organic cathode exhibits an accumulated capacity of 16264 mAh g, which enables the Zn-organic battery to show a record high energy density of 625.5 Wh kg.
锌有机电池正吸引着广泛关注,但其能量密度受到有机阴极低容量(<400 mAh g)和低电位(相对于Zn/Zn<1 V)的限制。在此,我们提出一种长寿命、高倍率的锌有机电池,其在碱性电解质中包含聚(1,5-萘二胺)阴极和锌阳极,其中阴极反应基于K与C═N基团之间的配位反应(即C═N/C-N-K转化)。有趣的是,我们发现放电后的锌有机电池在有O存在的情况下能迅速恢复到初始状态,理论计算表明放电阴极中的K-N键可被O通过氧化还原反应轻易破坏。因此,我们设计了一种化学自充电水系锌有机电池。受益于优异的自充电能力,有机阴极展现出16264 mAh g的累积容量,这使得锌有机电池能够展现出创纪录的625.5 Wh kg的高能量密度。