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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Sulfolane-Based Highly Concentrated Electrolytes of Lithium Bis(trifluoromethanesulfonyl)amide: Ionic Transport, Li-Ion Coordination, and Li-S Battery Performance
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Sulfolane-Based Highly Concentrated Electrolytes of Lithium Bis(trifluoromethanesulfonyl)amide: Ionic Transport, Li-Ion Coordination, and Li-S Battery Performance

机译:基于磺胺的基于锂双(三氟甲磺酰基)酰胺的高浓缩电解质:离子转运,锂离子配位和Li-S电池性能

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摘要

Following our recent study demonstrating predominant Li-ion hopping conduction in sulfolane (SL)-based highly concentrated electrolytes with LiBF4, LiClO4, and lithium bis(fluorosulfonyl)amide, herein a systematic study on transport properties and Li-ion coordination of SL-based electrolytes with lithium bis(trifluoromethanesulfonyl)amide was performed. In the highly concentrated region, Li ions clearly diffuse faster than SL and TFSA anions. The two oxygen atoms of the SL sulfonyl group tend to coordinate to two different neighboring Li ions and TFSA anions form ionic clusters with Li ions, verifying the previous observation of the unusual Li-ion conduction and its relevance to the SL-and anion-bridged, chainlike Li-ion coordination structure for the SL-based concentrated systems with other Li salts. Moreover, addition of hydrofluoroether (HFE) to the SL-based concentrated electrolytes greatly enhances diffusion coefficients but fragments the chainlike Li-ion coordination to smaller clusters, leading to a reduced contribution of Li-ion hopping to the overall Li-ion conduction. The SL-based concentrated electrolyte and its mixtures with HFE showed lower lithium polysulfide solubility and higher rate capability for lithium-sulfur (Li-S) cells compared with previously reported tetraglyme-based electrolytes. The SL-based electrolytes were found to manifest a significant improvement in Li-ion mass transfer as a sparingly solvating electrolyte, enabling the solid-state sulfur redox reactions in high-performance Li-S batteries.
机译:在我们最近的研究之后,在磺胺(SL)中,基于Libf4,LiClO4和双(氟磺酰基)酰胺的高度浓缩电解质,在本文中,在亚磺甲酰胺(SL)中的主要浓度电解质中,本文是对SL的转运性能和锂离子配位的系统研究用锂双(三氟甲磺酰基)酰胺的电解质进行。在高度浓缩区域中,Li离子明显弥漫于SL和TFSA阴离子。 SL磺酰基的两个氧原子倾向于与两个不同相邻的Li离子和TFSA阴离子与Li离子形成离子簇,验证了对不寻常的锂离子传导的先前观察及其与SL和阴离子桥接的相关性,与其他Li盐的SL基浓缩系统的链条状锂离子配位结构。此外,向基于SL的浓缩电解质中加入氢氟醚(HFE)极大地增强了扩散系数,但将链状的锂离子配件片段分离为较小的簇,导致锂离子跳跃到整个锂离子传导的贡献。与先前报道的四平均电解质相比,SL基浓缩电解质及其HFE的混合物显示出较低的多硫化锂溶解度和锂 - 硫(Li-S)细胞的较高速率能力。发现SL基电解质表现出锂离子质量转移的显着改善,作为静脉溶剂电解质,使高性能Li-S电池中的固态硫氧化还原反应能够。

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    Yokohama Natl Univ Dept Chem &

    Biotechnol Hodogaya Ku 79-5 Tokiwadai Yokohama Kanagawa 2408501 Japan;

    Yokohama Natl Univ Dept Chem &

    Biotechnol Hodogaya Ku 79-5 Tokiwadai Yokohama Kanagawa 2408501 Japan;

    Yokohama Natl Univ Dept Chem &

    Biotechnol Hodogaya Ku 79-5 Tokiwadai Yokohama Kanagawa 2408501 Japan;

    Yokohama Natl Univ Dept Chem &

    Biotechnol Hodogaya Ku 79-5 Tokiwadai Yokohama Kanagawa 2408501 Japan;

    Yokohama Natl Univ Dept Chem &

    Biotechnol Hodogaya Ku 79-5 Tokiwadai Yokohama Kanagawa 2408501 Japan;

    Yokohama Natl Univ Dept Chem &

    Biotechnol Hodogaya Ku 79-5 Tokiwadai Yokohama Kanagawa 2408501 Japan;

    Yokohama Natl Univ Dept Chem &

    Biotechnol Hodogaya Ku 79-5 Tokiwadai Yokohama Kanagawa 2408501 Japan;

    Yokohama Natl Univ Dept Chem &

    Biotechnol Hodogaya Ku 79-5 Tokiwadai Yokohama Kanagawa 2408501 Japan;

    Yokohama Natl Univ Dept Chem &

    Biotechnol Hodogaya Ku 79-5 Tokiwadai Yokohama Kanagawa 2408501 Japan;

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  • 正文语种 eng
  • 中图分类 物理化学(理论化学)、化学物理学;
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