Yu Haiping, Li Rui, Wang Zhihui, Wang Bei, Li Mengxiao, Zhao Guoqing, Wang Xinyu, Yan Xiaorong, Hao Yuxin, Ma Huige, Liu Jingru, Hu Mingjun, Yang Jun
Beijing Institute of Nanoenergy & Nanosystems, Chinese Academy of Sciences Beijing 101400 China
School of Nanoscience and Engineering, University of Chinese Academy of Sciences Beijing 101408 China.
Chem Sci. 2025 Jun 3. doi: 10.1039/d5sc02677f.
Rechargeable aqueous batteries are regarded as promising candidates for large-scale energy storage with the advantages of cost-effectiveness, environmentally friendliness, and innate safety. However, to date, most of the aqueous ion batteries that have been reported are equipped with metal cation charge carriers and encounter either poor sustainability or low reaction activity. Here, we first reported an aqueous imidazolium-ion battery with MMZ-H/H as co-intercalated ions. In detail, we configured an almost neutral electrolyte with a wide electrochemical window of 2.66 V by adding an appropriate amount of alkaline 1-methylimidazole (MMZ) to 0.5 M HSO, and named it 50M-10S electrolyte. Due to the strong binding energy between MMZ and H, MMZ-H as an entire unit can be inserted into or extracted from the HATN-3CN (hexaazatrinaphthalene-2,8,14-tricarbonitrile) electrode. The MMZ-H and H co-insertion increases the capacity by 40% compared to pure H insertion in this proton battery (287.6 mAh g in 50M-10S electrolyte 206.8 mAh g in 0.5 M HSO electrolyte, 0.1 A g). Theoretical calculations illustrated that the insertion of MMZ-H can further activate the unreacted N active sites due to their enhanced nucleophilicity derived from stronger electron-donating ability of ionized nitrogen sites than the protonated one. Moreover, the assembled full batteries also exhibit ultra-high specific capacity (266.6 mAh g, 1 A g) and ultra-slow degradation (capacity retention of 97%, 1 A g, 1000 cycles). This research further enriches the library of inserted ions and will help to understand and enhance proton storage in near-neutral electrolytes and build new battery models.
可充电水系电池因其成本效益高、环境友好和本质安全等优点,被视为大规模储能的有前景的候选者。然而,迄今为止,已报道的大多数水系离子电池都配备有金属阳离子电荷载体,并且存在可持续性差或反应活性低的问题。在此,我们首次报道了一种以MMZ-H/H作为共嵌入离子的水系咪唑离子电池。具体而言,我们通过向0.5 M HSO中加入适量的碱性1-甲基咪唑(MMZ),配置了一种具有2.66 V宽电化学窗口的近中性电解质,并将其命名为50M-10S电解质。由于MMZ与H之间的强结合能,MMZ-H作为一个整体单元可以插入到HATN-3CN(六氮杂三萘-2,8,14-三腈)电极中或从其中脱出。与该质子电池中纯H嵌入相比,MMZ-H和H的共嵌入使容量提高了40%(在50M-10S电解质中为287.6 mAh g,在0.5 M HSO电解质中为206.8 mAh g,0.1 A g)。理论计算表明,MMZ-H的嵌入可以进一步激活未反应的N活性位点,这是由于其离子化氮位点比质子化氮位点具有更强的给电子能力,从而增强了亲核性。此外,组装的全电池还表现出超高的比容量(266.6 mAh g,1 A g)和极慢的降解(容量保持率为97%,1 A g,1000次循环)。这项研究进一步丰富了嵌入离子的库,并将有助于理解和增强近中性电解质中的质子存储以及构建新的电池模型。