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超薄离子液体膜的液/固界面:在 Au(111)上的 [C1C1Im][Tf2N] 和 [C8C1Im][Tf2N]。

Liquid/solid interface of ultrathin ionic liquid films: [C1C1Im][Tf2N] and [C8C1Im][Tf2N] on Au(111).

机构信息

Lehrstuhl für Physikalische Chemie II and Erlangen Catalysis Resource Center, Friedrich-Alexander-Universität, Erlangen-Nürnberg Egerlandstrasse 3, 91058 Erlangen, Germany.

出版信息

Langmuir. 2011 Apr 5;27(7):3662-71. doi: 10.1021/la105007c. Epub 2011 Mar 1.

Abstract

Ultrathin films of two imidazolium-based ionic liquids (IL), [C(1)C(1)Im][Tf(2)N] (= 1,3-dimethylimidazolium bis(trifluoromethyl)imide) and [C(8)C(1)Im][Tf(2)N] (= 1-methyl-3-octylimidazolium bis(trifluoromethyl)imide) were prepared on a Au(111) single-crystal surface by physical vapor deposition in ultrahigh vacuum. The adsorption behavior, orientation, and growth were monitored via angle-resolved X-ray photoelectron spectroscopy (ARXPS). Coverage-dependent chemical shifts of the IL-derived core levels indicate that for both ILs the first layer is formed from anions and cations directly in contact with the Au surface in a checkerboard arrangement and that for [C(8)C(1)Im][Tf(2)N] a reorientation of the alkyl chain with increasing coverage is found. For both ILs, geometry models of the first adsorption layer are proposed. For higher coverages, both ILs grow in a layer-by-layer fashion up to thicknesses of at least 9 nm (>10 ML). Moreover, beam damage effects are discussed, which are mainly related to the decomposition of Tf(2)N anions directly adsorbed at the gold surface.

摘要

通过在超高真空条件下的物理气相沉积,在 Au(111)单晶表面制备了两种咪唑鎓基离子液体(IL)的超薄膜,[C(1)C(1)Im][Tf(2)N](= 1,3-二甲基咪唑双(三氟甲基)亚胺)和[C(8)C(1)Im][Tf(2)N](= 1-甲基-3-辛基咪唑双(三氟甲基)亚胺)。通过角度分辨 X 射线光电子能谱(ARXPS)监测吸附行为、取向和生长。IL 衍生的芯层的覆盖度依赖性化学位移表明,对于两种 IL,第一层是由与 Au 表面直接接触的阴离子和阳离子以棋盘格排列形成的,并且对于[C(8)C(1)Im][Tf(2)N],随着覆盖度的增加,烷基链发生重排。对于这两种 IL,都提出了第一层吸附的几何模型。对于更高的覆盖度,两种 IL 都以逐层方式生长,厚度至少为 9nm(>10 ML)。此外,还讨论了束流损伤效应,这主要与直接吸附在金表面上的Tf(2)N阴离子的分解有关。

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