Lu Wenqiang, Zheng Tianfang, Zhang Xinyuan, He Tianmin, Sun Yuxin, Li Shuyang, Guan Buyuan, Zhang Dong, Wei Zhixuan, Jiang Heng, Fan Hong Jin, Du Fei
Key Laboratory of Physics and Technology for Advanced Batteries (Ministry of Education), State Key Laboratory of Superhard Materials, College of Physics, Jilin University, Changchun, 130012, P. R. China.
School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore, 637371, Singapore.
Angew Chem Int Ed Engl. 2025 Jan 27;64(5):e202417171. doi: 10.1002/anie.202417171. Epub 2024 Nov 14.
Aqueous manganese ion batteries hold potential for stationary storage applications owing to their merits in cost, energy density, and environmental sustainability. However, the formidable challenge is the instability of metallic manganese (Mn) anodes in aqueous electrolytes due to severe hydrogen evolution reaction (HER), which is more serious than the commonly studied Zn metal anodes. Moreover, the mechanism of HER side reactions has remained unclear. Herein, we design a series of Mn-P alloying anodes by precisely regulating their energy band structures to mitigate the HER issue. It is found that the serious HER primarily originates from the spontaneous Mn-HO reaction driven by the excessively high HOMO energy level of Mn, rather than electrocatalytic water splitting. Owing to a reduced HOMO energy level and enhanced electron escape work function, the MnP anode achieves an evidently enhanced cycle durability (over 1000 hours at a high current density of 5 mA cm). The MnP||AgVO full cell with an N/P ratio of 4 exhibits better rate capability and extended cycle life (7000 cycles) with minimal capacity degradation than the cell using metallic Mn anode (less than 100 cycles). This study provides a practical approach for developing highly durable aqueous Mn ion batteries.
水系锰离子电池因其在成本、能量密度和环境可持续性方面的优点,在固定式储能应用中具有潜力。然而,巨大的挑战是金属锰(Mn)负极在水系电解质中由于严重的析氢反应(HER)而不稳定,这比通常研究的锌金属负极更为严重。此外,HER副反应的机理仍不清楚。在此,我们通过精确调节其能带结构设计了一系列Mn-P合金负极,以缓解HER问题。研究发现,严重的HER主要源于Mn过高的最高占据分子轨道(HOMO)能级驱动的自发Mn-HO反应,而非电催化水分解。由于HOMO能级降低和电子逸出功函数增强,MnP负极实现了显著增强的循环耐久性(在5 mA cm的高电流密度下超过1000小时)。与使用金属Mn负极的电池(少于100次循环)相比,N/P比为4的MnP||AgVO全电池表现出更好的倍率性能和更长的循环寿命(7000次循环),容量衰减最小。本研究为开发高度耐用的水系锰离子电池提供了一种实用方法。