{"title":"利用高供体溶剂和醇阴离子受体的协同作用设计电解质,用于可逆氟离子电池","authors":"Guyue Li, Yifan Yu, Decheng Li, Chilin Li","doi":"10.1002/adfm.202406421","DOIUrl":null,"url":null,"abstract":"<p>Fluoride ion batteries (FIBs) are regarded as one of the most promising candidates for next-generation energy storage systems to achieve lower cost and higher energy density. However, the appropriate electrolyte design strategy is still lacking for FIBs to simultaneously settle the issues of fluoride salt dissolution and metal cation shuttle. Herein, a novel fluoride ion shuttle electrolyte with the synergistic high-donor solvent (N, N-dimethylacetamide, DMA) and alcohol anion acceptor (benzyl alcohol, BA) is developed. BA enables the promotion of solubility of inorganic fluoride salt (CsF). Meanwhile, benefiting from the re-configuration of hydrogen bonding network by DMA, the solvation structures of anions and cations are regulated with reduced hindrance to F<sup>−</sup> shuttle and mitigated dissolution of active material. This electrolyte formation achieves superior interfacial stability with cathode, high F<sup>−</sup> conductivity (2.05 mS cm<sup>−1</sup>), and transference number (0.53). After matching CuF<sub>2</sub> cathode and Pb anode, the full cell exhibits the highly reversible conversion reaction process with an initial discharge capacity of 300.8 mAh g<sup>−1</sup> and a reversible capacity of 245.5 mAh g<sup>−1</sup> after 43 cycles. This study proposes a solution to high-performance rechargeable FIBs at room temperature by synergistically manipulating the anionic and cationic solvation chemistry.</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"34 41","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2024-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrolyte Design by Synergistic High-Donor Solvent and Alcohol Anion Acceptor for Reversible Fluoride Ion Batteries\",\"authors\":\"Guyue Li, Yifan Yu, Decheng Li, Chilin Li\",\"doi\":\"10.1002/adfm.202406421\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Fluoride ion batteries (FIBs) are regarded as one of the most promising candidates for next-generation energy storage systems to achieve lower cost and higher energy density. However, the appropriate electrolyte design strategy is still lacking for FIBs to simultaneously settle the issues of fluoride salt dissolution and metal cation shuttle. Herein, a novel fluoride ion shuttle electrolyte with the synergistic high-donor solvent (N, N-dimethylacetamide, DMA) and alcohol anion acceptor (benzyl alcohol, BA) is developed. BA enables the promotion of solubility of inorganic fluoride salt (CsF). Meanwhile, benefiting from the re-configuration of hydrogen bonding network by DMA, the solvation structures of anions and cations are regulated with reduced hindrance to F<sup>−</sup> shuttle and mitigated dissolution of active material. This electrolyte formation achieves superior interfacial stability with cathode, high F<sup>−</sup> conductivity (2.05 mS cm<sup>−1</sup>), and transference number (0.53). After matching CuF<sub>2</sub> cathode and Pb anode, the full cell exhibits the highly reversible conversion reaction process with an initial discharge capacity of 300.8 mAh g<sup>−1</sup> and a reversible capacity of 245.5 mAh g<sup>−1</sup> after 43 cycles. This study proposes a solution to high-performance rechargeable FIBs at room temperature by synergistically manipulating the anionic and cationic solvation chemistry.</p>\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"34 41\",\"pages\":\"\"},\"PeriodicalIF\":19.0000,\"publicationDate\":\"2024-07-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/adfm.202406421\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/adfm.202406421","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
氟离子电池(FIBs)被认为是下一代储能系统中最有希望实现低成本和高能量密度的候选产品之一。然而,氟离子电池仍缺乏合适的电解质设计策略,以同时解决氟化盐溶解和金属阳离子穿梭的问题。本文开发了一种新型氟离子穿梭电解质,该电解质具有高供体溶剂(N, N-二甲基乙酰胺,DMA)和醇阴离子受体(苄醇,BA)的协同作用。BA 可提高无机氟化盐(CsF)的溶解度。同时,得益于 DMA 对氢键网络的重新配置,阴阳离子的溶解结构得到调节,减少了对 F- 穿梭的阻碍,并减轻了活性材料的溶解。这种电解质与阴极的界面稳定性极佳,具有很高的 F- 导电性(2.05 mS cm-1)和转移数(0.53)。将 CuF2 阴极和铅阳极配对后,整个电池呈现出高度可逆的转换反应过程,初始放电容量为 300.8 mAh g-1,43 个循环后的可逆容量为 245.5 mAh g-1。本研究提出了一种通过协同操纵阴离子和阳离子溶解化学作用在室温下实现高性能可充电 FIB 的解决方案。
Electrolyte Design by Synergistic High-Donor Solvent and Alcohol Anion Acceptor for Reversible Fluoride Ion Batteries
Fluoride ion batteries (FIBs) are regarded as one of the most promising candidates for next-generation energy storage systems to achieve lower cost and higher energy density. However, the appropriate electrolyte design strategy is still lacking for FIBs to simultaneously settle the issues of fluoride salt dissolution and metal cation shuttle. Herein, a novel fluoride ion shuttle electrolyte with the synergistic high-donor solvent (N, N-dimethylacetamide, DMA) and alcohol anion acceptor (benzyl alcohol, BA) is developed. BA enables the promotion of solubility of inorganic fluoride salt (CsF). Meanwhile, benefiting from the re-configuration of hydrogen bonding network by DMA, the solvation structures of anions and cations are regulated with reduced hindrance to F− shuttle and mitigated dissolution of active material. This electrolyte formation achieves superior interfacial stability with cathode, high F− conductivity (2.05 mS cm−1), and transference number (0.53). After matching CuF2 cathode and Pb anode, the full cell exhibits the highly reversible conversion reaction process with an initial discharge capacity of 300.8 mAh g−1 and a reversible capacity of 245.5 mAh g−1 after 43 cycles. This study proposes a solution to high-performance rechargeable FIBs at room temperature by synergistically manipulating the anionic and cationic solvation chemistry.
期刊介绍:
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