{"title":"Ternary Potassium Single Cation Ionic Liquid Electrolyte for Potassium Secondary Batteries.","authors":"Hiroki Yamamoto, Keigo Kubota, Jinkwang Hwang, Kazuhiko Matsumoto, Rika Hagiwara","doi":"10.1021/acs.jpcb.4c08105","DOIUrl":null,"url":null,"abstract":"<p><p>Potassium single cation ionic liquids (K-SCILs), which solely contain K<sup>+</sup> as the cationic species, realize exceptionally high K<sup>+</sup> concentrations and exhibit unique physicochemical and electrochemical properties. However, K-SCILs tend to have high melting points due to the smaller size of K<sup>+</sup> than those of bulky organic cations, resulting in high operating temperatures for battery applications. In this study, a K-SCIL with a melting point below that of K metal (64 °C) was developed by evolving a binary system to a ternary one. The resulting K-SCIL, K[FSA]<sub>0.33</sub>[FTA]<sub>0.33</sub>[TfO]<sub>0.33</sub> (FSA<sup>-</sup>: bis(fluorosulfonyl)amide, FTA<sup>-</sup>: (fluorosulfonyl)(trifluoromethanesulfonyl)amide, and TfO<sup>-</sup>: trifluoromethanesulfonate), has a low melting point of 50 °C with a high K<sup>+</sup> concentration of 9.3 mol dm<sup>-3</sup> at 55 °C. It allows the safe handling of K metal and exhibits improved solid K metal deposition/dissolution compared to a conventional organic electrolyte. The K-SCIL does not involve the formation of a K<sup>+</sup> concentration gradient near the electrode surface, which is demonstrated by the applicability of large currents exceeding a limiting current density assumed by calculation. Furthermore, stable K<sup>+</sup> intercalation/deintercalation into/from graphite was successfully demonstrated at 55 °C, highlighting the potential of this K-SCIL for advanced potassium battery applications.</p>","PeriodicalId":60,"journal":{"name":"The Journal of Physical Chemistry B","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry B","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpcb.4c08105","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Potassium single cation ionic liquids (K-SCILs), which solely contain K+ as the cationic species, realize exceptionally high K+ concentrations and exhibit unique physicochemical and electrochemical properties. However, K-SCILs tend to have high melting points due to the smaller size of K+ than those of bulky organic cations, resulting in high operating temperatures for battery applications. In this study, a K-SCIL with a melting point below that of K metal (64 °C) was developed by evolving a binary system to a ternary one. The resulting K-SCIL, K[FSA]0.33[FTA]0.33[TfO]0.33 (FSA-: bis(fluorosulfonyl)amide, FTA-: (fluorosulfonyl)(trifluoromethanesulfonyl)amide, and TfO-: trifluoromethanesulfonate), has a low melting point of 50 °C with a high K+ concentration of 9.3 mol dm-3 at 55 °C. It allows the safe handling of K metal and exhibits improved solid K metal deposition/dissolution compared to a conventional organic electrolyte. The K-SCIL does not involve the formation of a K+ concentration gradient near the electrode surface, which is demonstrated by the applicability of large currents exceeding a limiting current density assumed by calculation. Furthermore, stable K+ intercalation/deintercalation into/from graphite was successfully demonstrated at 55 °C, highlighting the potential of this K-SCIL for advanced potassium battery applications.
期刊介绍:
An essential criterion for acceptance of research articles in the journal is that they provide new physical insight. Please refer to the New Physical Insights virtual issue on what constitutes new physical insight. Manuscripts that are essentially reporting data or applications of data are, in general, not suitable for publication in JPC B.