Spectroscopic study of ionic liquid adsorption from solution onto gold

被引:30
作者
Beattie, David A. [1 ]
Harmer-Bassell, Sarah L. [2 ]
Ho, Tracey T. M. [1 ]
Krasowska, Marta [1 ]
Ralston, John [1 ]
Sellapperumage, Pasindu M. F. [1 ]
Wasik, Patryk [1 ]
机构
[1] Univ S Australia, Ian Wark Res Inst, Adelaide, SA 5095, Australia
[2] Flinders Univ South Australia, Sch Chem & Phys Sci, Bedford Pk, SA 5042, Australia
基金
澳大利亚研究理事会; 瑞士国家科学基金会;
关键词
RAY PHOTOELECTRON-SPECTROSCOPY; SELF-ASSEMBLED MONOLAYERS; DIFFERENTIAL CAPACITANCE; ANTIWEAR PERFORMANCE; ALLOY SURFACES; DOUBLE-LAYER; FILMS; INTERFACE; AU(111); TEMPERATURE;
D O I
10.1039/c4cp05558f
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
Gold was exposed to ethanol solutions containing 0.1 wt% 1-hexyl-3-methyl-imidazolium bis(trifluoromethanesulfonyl) imide (HMIM NTf2), an ionic liquid (IL). The resulting adsorbed layers were interrogated using X-ray photoelectron spectroscopy (XPS - both conventional and synchrotron-based) and spectroscopic ellipsometry. Ellipsometry indicated that the adsorbed layer thickness was smaller than the size of an IL ion pair, with an average determined layer thickness of 0.15 nm. This value indicates that the adsorbed layer on gold is most likely patchy. Conventional XPS revealed that the IL adsorbs irreversibly to gold, with equal amounts of anion and cation in the adsorbed layer. High signal-to- noise synchrotron XPS spectra permitted detailed deconvolution of the S 2p and N 1s peaks for the IL-treated gold, providing more information on adsorbed layer composition and structure. Spectra acquired as a function of X-ray exposure time indicate that non-interacting physisorbed IL components are preferentially removed at the expense of surface bound components, and that anion and cation are both present in the surface bound layer, and also in the layer above. A model structure for the IL adsorbed on gold is proposed.
引用
收藏
页码:4199 / 4209
页数:11
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