A time-of-flight secondary ion mass spectroscopy study of 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide RT-ionic liquid

被引:35
作者
Guenster, Jens [1 ]
Hoefft, Oliver [2 ]
Krischok, Stefan [3 ,4 ]
Souda, Ryutaro [5 ]
机构
[1] Natl Inst Mat Sci, Int Ctr Young Scientists, Tsukuba, Ibaraki 3050044, Japan
[2] Tech Univ Clausthal, Inst Met, D-38678 Clausthal Zellerfeld, Germany
[3] Tech Univ Ilmenau, Inst Phys, D-98684 Ilmenau, Germany
[4] Tech Univ Ilmenau, Inst Mikro & Nanotechnol, D-98684 Ilmenau, Germany
[5] Natl Inst Mat Sci, Nanoscale Mat Ctr, Tsukuba, Ibaraki 3050044, Japan
关键词
TOF-SIMS; Ionic liquids; Crystallization; Glass-liquid transition;
D O I
10.1016/j.susc.2008.09.018
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
Time-of-flight secondary ion mass spectroscopy (TOF-SIMS) has been used to investigate the surface structural transformation of room temperature ionic liquid, 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imid ([EMIM][Tf2N]), in the temperature range between 300 and 160 K. The intensity of the [EMIM](+) cation from the crystal surface becomes about twice as large as that from the glassy and liquid surfaces, whereas the fragment ions from the [Tf2N](-) moiety are almost unchanged upon crystallization. This phenomenon can be ascribed to the steric effect of the cation relative to the counter anion at the topmost surface layer rather than their surface compositions: a specific layered structure of the crystal surface, in which the imidazolium ring of [EMIM](+) is aligned parallel to the surface plane, is thought to be responsible for the enhancement of the [EMIM](+) ion emission. The smaller [EMIM](+) intensity from the glassy and liquid films evidences that the imidazolium ring is not parallel to the surface. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:3403 / 3407
页数:5
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