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通过化学交联的环氧乙烷途径增强聚(乙二醇)二丙烯酸酯支撑溶剂化离子凝胶电解质中的锂离子传输。

Enhanced Lithium Ion Transport in Poly(ethylene glycol) Diacrylate-Supported Solvate Ionogel Electrolytes via Chemically Cross-linked Ethylene Oxide Pathways.

机构信息

Department of Chemical & Biological Engineering Tufts University , 4 Colby Street, Medford, Massachusetts 02155, United States.

出版信息

J Phys Chem B. 2017 Feb 2;121(4):890-895. doi: 10.1021/acs.jpcb.6b10125. Epub 2017 Jan 24.

Abstract

Lithium-ion solvate ionic liquids (SILs), consisting of complexed Li cations and a weakly basic anion, represent an emergent class of nonvolatile liquid electrolytes suitable for lithium-based electrochemical energy storage. In this report, solid-state, flexible solvate ionogel electrolytes are synthesized via UV-initiated free radical polymerization/cross-linking of poly(ethylene glycol) diacrylate (PEGDA) in situ within the [Li(G4)][TFSI] electrolyte, which is formed by an equimolar mixture of lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) and tetraglyme (G4). Ion diffusivity measurements reveal enhanced Li diffusion in PEGDA-supported solvate ionogels, as compared to poly(methyl methacrylate)-supported gels that lack ethylene oxide chains. At 21 vol% PEGDA, a maximum Li transport number of 0.58 and a room temperature ionic conductivity of 0.43 mS/cm have been achieved in a solvate ionogel electrolyte that exhibits an elastic modulus of 0.47 MPa. These results demonstrate the importance of polymer scaffold selection on solvate ionogel electrolyte performance for advanced lithium-based batteries.

摘要

锂离子溶剂化离子液体(SILs)由配位的 Li 阳离子和弱碱性阴离子组成,代表了一类新兴的非挥发性液体电解质,适用于基于锂的电化学储能。在本报告中,通过在 [Li(G4)][TFSI] 电解质中进行原位的聚乙二醇二丙烯酸酯(PEGDA)的 UV 引发自由基聚合/交联,合成了固态、柔性溶剂化离子凝胶电解质,[Li(G4)][TFSI] 电解质由等摩尔比的双(三氟甲基磺酰基)亚胺锂(LiTFSI)和四甘醇(G4)形成。与缺乏环氧乙烷链的聚甲基丙烯酸甲酯(PMMA)支撑凝胶相比,离子扩散测量表明,PEGDA 支撑的溶剂化离子凝胶中的 Li 扩散得到了增强。在 21vol%PEGDA 下,在具有 0.47MPa 弹性模量的溶剂化离子凝胶电解质中,实现了 0.58 的最大 Li 迁移数和 0.43mS/cm 的室温离子电导率。这些结果表明,对于先进的基于锂的电池,聚合物支架选择对溶剂化离子凝胶电解质性能的重要性。

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