Fluoride-Based Deep Eutectic Solvents with Amide Dual-Hydrogen-Bond Donors

被引:1
|
作者
Yamamoto, Hiroki [1 ]
Hattori, Mineyuki [2 ]
Ito, Kenji [2 ]
Shikano, Masahiro [1 ,3 ]
Yoshii, Kazuki [1 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Res Inst Electrochem Energy, Dept Energy & Environm, Ikeda, Osaka 5638577, Japan
[2] Res Inst Mat & Chem Measurement, Natl Metrol Inst Japan, Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058565, Japan
[3] Natl Inst Adv Ind Sci & Technol, Fukushima Renewable Energy Inst, Koriyama, Fukushima 9630298, Japan
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2024年 / 15卷 / 24期
基金
日本学术振兴会;
关键词
FLUORINATION; DERIVATIVES; SOLVATION; SPECTRA; UREA;
D O I
10.1021/acs.jpclett.4c01085
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Developing F--containing electrolytes is crucial for electrochemical and chemical fluorination. However, balancing the F- concentration and electrochemical stability of the electrolytes remains a challenge. In this study, fluoride-based deep eutectic solvents (F-DESs) were obtained by using amide hydrogen-bond donors (HBDs) containing dual N-H bonds. The obtained F-DES, [TMA]F center dot 3.5[1,3-DMU], was prepared by facilely mixing solid compounds of tetramethylammonium fluoride ([TMA]F) and 1,3-dimethylurea (1,3-DMU), resulting in a high F- concentration (2.6 mol dm(-3)) and a wide electrochemical window (3.1 V) at room temperature. The electrochemical window was much wider than that of [TMA]F center dot 3.5[EG] (EG, ethylene glycol) as another F-DES with an alcohol HBD (1.9 V). Moreover, [TMA]F center dot 3.5[1,3-DMU] exhibited an ionic conductivity that was 2 orders of magnitude higher than that of [TMA]F center dot 3.5[1,3-DMTU] (1,3-DMTU, 1,3-dimethylthiourea) around room temperature because of the bifurcated hydrogen bonds between the dual N-H bonds of 1,3-DMU and one F-. Thus, [TMA]F center dot 3.5[1,3-DMU] was demonstrated to be applicable to electrochemical fluorination.
引用
收藏
页码:6249 / 6255
页数:7
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