Haiping Yu, Zhihui Wang, Mengxiao Li, Mingjun Hu, Jun Yang, Rui Li, Bei Wang, Guoqing Zhao, Xinyu Wang, Xiaorong Yan, Yuxin Hao, Huige Ma, Jingru Liu
{"title":"High-capacity aqueous imidazolium-ion battery enabled by MMZ-H+/H+ co-intercalation in a near neutral electrolyte","authors":"Haiping Yu, Zhihui Wang, Mengxiao Li, Mingjun Hu, Jun Yang, Rui Li, Bei Wang, Guoqing Zhao, Xinyu Wang, Xiaorong Yan, Yuxin Hao, Huige Ma, Jingru Liu","doi":"10.1039/d5sc02677f","DOIUrl":null,"url":null,"abstract":"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 H2SO4, named as 50M-10S electrolyte. Due to the strong binding energy between MMZ and H+, the MMZ-H+ as an entire unit can insert into or extract from 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-1 in 50M-10S electrolyte vs. 206.8 mAh g-1 in 0.5 M H2SO4 electrolyte, 0.1 A g-1). 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, 1 A g-1) and ultra-slow degradation (capacity retention of 97 %, 1 A g-1, 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 model.","PeriodicalId":9909,"journal":{"name":"Chemical Science","volume":"169 1","pages":""},"PeriodicalIF":7.6000,"publicationDate":"2025-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Science","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5sc02677f","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
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 H2SO4, named as 50M-10S electrolyte. Due to the strong binding energy between MMZ and H+, the MMZ-H+ as an entire unit can insert into or extract from 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-1 in 50M-10S electrolyte vs. 206.8 mAh g-1 in 0.5 M H2SO4 electrolyte, 0.1 A g-1). 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, 1 A g-1) and ultra-slow degradation (capacity retention of 97 %, 1 A g-1, 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 model.
可充电水电池具有成本效益高、环境友好、固有安全等优点,被认为是大规模储能的理想选择。然而,迄今为止,大多数已报道的水性离子电池都配备了金属阳离子载流子,并且存在可持续性差或反应活性低的问题。在这里,我们首次报道了一种以MMZ-H+/H+为共插层离子的水相咪唑离子电池。我们在0.5 M H2SO4中加入适量的碱性1-甲基咪唑(MMZ),配置了一种电化学窗口宽为2.66 V的几乎中性的电解质,命名为50M-10S电解质。由于MMZ与H+之间的强结合能,MMZ-H+作为一个整体可以插入或从HATN-3CN(六氮杂萘-2,8,14-三碳腈)电极中提取。与纯氢离子插入相比,MMZ-H+和H+的共插入可增加40%的容量(50M-10S电解液中287.6 mAh g-1, 0.5 M H2SO4电解液中206.8 mAh g-1, 0.1 A g-1)。理论计算表明,MMZ-H+的插入可以进一步激活未反应的N活性位点,这是由于电离态氮的给电子能力比质子化态氮的给电子能力强,从而增强了N活性位点的亲核性。此外,组装的完整电池还具有超高的比容量(266.6 mAh g-1, 1 A g-1)和超慢的退化(容量保持97%,1 A g-1, 1000次循环)。该研究进一步丰富了插入离子库,有助于理解和增强近中性电解质中的质子存储,并建立新的电池模型。
期刊介绍:
Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.