論文

査読有り
2016年7月

Li+ Local Structure in Li-Tetraglyme Solvate Ionic Liquid Revealed by Neutron Total Scattering Experiments with the Li-6/7 Isotopic Substitution Technique

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
  • Soshi Saito
  • Hikari Watanabe
  • Yutaka Hayashi
  • Masaru Matsugami
  • Seiji Tsuzuki
  • Shiro Seki
  • Jose N. Canongia Lopes
  • Rob Atkin
  • Kazuhide Ueno
  • Kaoru Dokko
  • Masayoshi Watanabe
  • Yasuo Kameda
  • Yasuhiro Umebayashi
  • 全て表示

7
14
開始ページ
2832
終了ページ
2837
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1021/acs.jpclett.6b01266
出版者・発行元
AMER CHEMICAL SOC

Equimolar mixtures of lithium bis(trifluoromethanesulfonyl)amide (LiTFSA) and tetraglyme (G4: CH3O (CH2CH2O)(4)-CH3) yield the solvate (or chelate) ionic liquid [Li(G4)][TFSA], which is a homogeneous transparent solution at room temperature. Solvate ionic liquids (SILs) are currently attracting increasing research interest, especially as new electrolytes for Li sulfur batteries. Here, we performed neutron total scattering experiments with Li-6/7 isotopic substitution to reveal the Li+ solvation/local structure in [Li(G4)][TFSA] SILs. The experimental interference function and radial distribution function around Li+ agree well with predictions from ab initio calculations and MD simulations. The model solvation/local structure was optimized with,nonlinear least-squares analysis to yield structural parameters. The refined Li+ solvation/local structure in the [Li(G4)][TFSA] SIL shows that lithium cations are not coordinated to all five oxygen atoms of the G4 molecule (deficient five-coordination) but only to four of them (actual four-coordination). The solvate cation is thus considerably distorted, which can be ascribed to the limited phase space of the ethylene oxide chain and competition for coordination sites from the TFSA anion.

リンク情報
DOI
https://doi.org/10.1021/acs.jpclett.6b01266
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000380415400032&DestApp=WOS_CPL
ID情報
  • DOI : 10.1021/acs.jpclett.6b01266
  • ISSN : 1948-7185
  • Web of Science ID : WOS:000380415400032

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