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在固-液界面处,氰基官能化阴离子的咪唑鎓基离子液体的和频发生光谱。

Sum frequency generation spectroscopy of imidazolium-based ionic liquids with cyano-functionalized anions at the solid salt-liquid interface.

机构信息

Department of Chemistry, University of Houston, Houston, Texas 77204-5003, USA.

出版信息

J Phys Chem B. 2013 May 16;117(19):5939-49. doi: 10.1021/jp4019074. Epub 2013 May 7.

DOI:10.1021/jp4019074
PMID:23650965
Abstract

A surface-sensitive nonlinear vibrational spectroscopic technique, sum frequency generation (SFG), has been used to study cyano-containing ionic liquids in contact with two different solid salt surfaces. Specifically, the interfacial chemistry of BaF2(111) single-crystal and solid NaCl{100} surfaces in contact with ionic liquids such as [BMIM][SCN], [BMIM][DCA], [BMIM][TCM], and [EMIM][TCB] has been investigated. Spectral features in both C-H and C-N stretching regions were assigned, with a detailed discussion of the nature of surface interactions and ordering of the ionic liquid ions at the interface of the different crystals. Results showed that BMIM cations adhered closely via Coulombic interactions to the negatively charged NaCl{100} surface, while SCN, TCM, and DCA anions revealed a strong electrostatic affinity to the positively charged BaF2(111) surface. Ions of the ionic liquid adsorbed to the solid salt surface to form a Helmholtz-like electric double layer. The linear SCN anion has a particularly strong affinity to the BaF2(111) surface, resulting in a first layer of anions directly in contact with BaF2(111) containing an effective negative surface excess charge. This promoted ordering of the cations in the second layer to counter the charge excess. At the BaF2(111)-[EMIM][TCB] interface, however, a strongly bound layer of anions populating the first layer resulted in a much larger counterion charge delivered near the crystal salt surface than required to effectively neutralize the initial surface charge from the crystal. As a result, strong resonances from the cation were observed at the BaF2(111) surface, suggesting a more complicated structure of the double layer at the interface than a simple Helmholtz-type model.

摘要

一种对表面敏感的非线性振动光谱技术,和频产生(SFG),已被用于研究与两种不同固体盐表面接触的含氰离子液体。具体来说,研究了 BaF2(111)单晶和 NaCl{100}固体表面与离子液体如 [BMIM][SCN]、[BMIM][DCA]、[BMIM][TCM] 和 [EMIM][TCB] 接触时的界面化学。在 C-H 和 C-N 伸缩区域分配了光谱特征,并详细讨论了不同晶体界面处离子液体离子的表面相互作用和有序性的本质。结果表明,BMIM阳离子通过库仑相互作用紧密地附着在带负电荷的 NaCl{100}表面上,而 SCN、TCM 和 DCA阴离子则显示出与带正电荷的 BaF2(111)表面强烈的静电亲和力。离子液体离子吸附在固体盐表面上形成亥姆霍兹型双电层。线性 SCN阴离子对 BaF2(111)表面具有特别强的亲和力,导致第一层阴离子直接与 BaF2(111)接触,含有有效的负表面过剩电荷。这促进了第二层中阳离子的有序排列以抵消电荷过剩。然而,在 BaF2(111)-[EMIM][TCB]界面上,填充第一层的强结合阴离子层导致靠近晶体盐表面传递的反离子电荷远远超过有效中和晶体初始表面电荷所需的电荷。因此,在 BaF2(111)表面观察到阳离子的强共振,表明界面双层的结构比简单的亥姆霍兹型模型更为复杂。

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