Bao Zhuoheng, Lu Chengjie, Liu Qiang, Ye Fei, Li Weihuan, Zhou Yang, Pan Long, Duan Lunbo, Tang Hongjian, Wu Yuping, Hu Linfeng, Sun ZhengMing
School of Materials Science and Engineering, Southeast University, Nanjing, 211189, P. R. China.
School of Energy and Environment, Southeast University, Nanjing, 211189, P. R. China.
Nat Commun. 2024 Mar 2;15(1):1934. doi: 10.1038/s41467-024-46317-5.
Ammonium ion batteries are promising for energy storage with the merits of low cost, inherent security, environmental friendliness, and excellent electrochemical properties. Unfortunately, the lack of anode materials restricts their development. Herein, we utilized density functional theory calculations to explore the VCT MXene as a promising anode with a low working potential. VCT MXene demonstrates pseudocapacitive behavior for ammonium ion storage, delivering a high specific capacity of 115.9 mAh g at 1 A g and excellent capacity retention of 100% after 5000 cycles at 5 A g. In-situ electrochemical quartz crystal microbalance measurement verifies a two-step electrochemical process of this unique pseudocapacitive storage behavior in the ammonium acetate electrolyte. Theoretical simulation reveals reversible electron transfer reactions with [NH(HAc)]···O coordination bonds, resulting in a superior ammonium ion storage capacity. The generality of this acetate ion enhancement effect is also confirmed in the MoS-based ammonium-ion battery system. These findings open a new door to realizing high capacity on ammonium ion storage through acetate ion enhancement, breaking the capacity limitations of both Faradaic and non-Faradaic energy storage.
铵离子电池因其低成本、固有安全性、环境友好性和优异的电化学性能等优点,在能量存储方面具有广阔前景。不幸的是,阳极材料的缺乏限制了它们的发展。在此,我们利用密度泛函理论计算来探索VCT MXene作为一种具有低工作电位的有前景的阳极材料。VCT MXene在铵离子存储方面表现出赝电容行为,在1 A g电流密度下具有115.9 mAh g的高比容量,在5 A g电流密度下循环5000次后容量保持率达100%。原位电化学石英晶体微天平测量验证了在醋酸铵电解质中这种独特的赝电容存储行为的两步电化学过程。理论模拟揭示了与[NH(HAc)]···O配位键的可逆电子转移反应,从而实现了优异的铵离子存储容量。在基于MoS的铵离子电池系统中也证实了这种醋酸根离子增强效应的普遍性。这些发现为通过醋酸根离子增强实现高容量铵离子存储打开了一扇新的大门,突破了法拉第和非法拉第能量存储的容量限制。