Aqueous, Mixed Micelles as a Means of Delivering the Hydrophobic Ionic Liquid EMIM TFSI to Graphene Oxide Surfaces

被引:9
|
作者
Lashkari, Sima [1 ]
Chekini, Mahshid [1 ]
Pal, Rajinder [1 ]
Pope, Michael A. [1 ,2 ]
机构
[1] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[2] Univ Waterloo, Waterloo Inst Nanotechnol, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
TRITON X-100 MICELLES; NONIONIC AMPHIPHILE; HYDRATION; SOLVENT; NANOPARTICLES; AGGREGATION; SURFACTANTS; ADSORPTION; COPOLYMERS; SHAPE;
D O I
10.1021/acs.langmuir.1c02928
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Most ionic liquids (ILs) are not surface-active and cannot, alone, be directed to assemble at surfaces-despite their potential as nonvolatile structure-directing agents and use as advanced materials in a multitude of applications. In this work, we investigate aqueous systems of common nonionic surfactants (Triton X-100 and Tween 20), which we use to solubilize 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide. The resulting solution of mixed micelle leads to spontaneous adsorption of the IL/surfactant complex onto graphene oxide (GO) surfaces, forming a compact film. Adsorption isotherms generated by fluorescence labeling of the IL and surfactant phases are used to quantify the extent of adsorption. While sensitive to the GO dispersion concentration, upwards of 3 g IL/g GO adsorb under dilute conditions. Atomic force microscopy is used to show that the adsorbed layer uniformly distributes as an similar to 1 nm thick coating (per GO side) as the system reaches the first plateau of a Langmuir-type isotherm. Adsorption beyond this plateau is possible but leads to thicker (>30 nm), inhomogeneous adsorbed layers. Both micellar size in solution and adsorbed layer thickness reduce upon the addition of IL to the surfactant phase, suggesting significant interactions among the materials and nonideal mixing of the components.
引用
收藏
页码:531 / 540
页数:10
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