Structures of Ionic Liquids Having Both Anionic and Cationic Octyl Tails: Lamellar Vacuum Interface vs Sponge-Like Bulk Order

被引:45
作者
Amith, Weththasinghage Don [1 ]
Hettige, Jeevapani J. [1 ]
Castner, Edward W., Jr. [2 ]
Margulis, Claudio J. [1 ]
机构
[1] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
[2] Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ 08854 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2016年 / 7卷 / 19期
基金
美国国家科学基金会;
关键词
MOLECULAR-DYNAMICS METHOD; SUM-FREQUENCY GENERATION; PARTICLE MESH EWALD; ALKYL CHAIN-LENGTH; X-RAY-SCATTERING; ROOM-TEMPERATURE; PHOTOELECTRON-SPECTROSCOPY; ELECTRODE INTERFACE; SURFACE-COMPOSITION; FORCE-FIELD;
D O I
10.1021/acs.jpclett.6b01763
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
Numerous experimental and computational studies have shown that the structure of ionic liquids is significantly influenced by confinement and by interactions with interfaces. The nature of the interface can affect the immediate ordering of cations and anions, changing important rheological characteristics relevant to lubrication. Most studies suggest that such changes are local or short-ranged and that bulk properties are reestablished on a length scale of a few nanometers. The current study focuses on the 1-methyl-3-octylimidazolium octylsulfate ionic liquid for which both the cation and anion have moderate length linear alkyl tails. For this system, we find that the bulk phase is dominated by the very common sponge-like morphology characteristic of many ionic liquids. However, at the vacuum interface, a lamellar structure is observed that is not restricted to the vicinity of the surface but instead extends across the full 9 nm slab of our simulation. We suspect that in reality it could extend significantly beyond this.
引用
收藏
页码:3785 / 3790
页数:6
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