Chaal Lila, Pillier Françoise, Saidani Boualem, Joiret Suzanne, Pailleret Alain, Deslouis Claude
UPR 15 CNRS Interfaces et Systèmes Electrochimiques, University P et M. Curie, 4 Place Jussieu, 75252 Paris Cédex 05, France.
J Phys Chem B. 2006 Nov 2;110(43):21710-8. doi: 10.1021/jp061607q.
Cylindrical micelles prepared in aqueous solutions from cationic surfactants octadecyl trimethylammonium (OTA+) or cetyltrimethylammonium (CTA+) and parachlorobenzoate (PCB) counterion were successfully imaged after evaporation of water using tapping mode atomic force microscopy (TM-AFM) onto very smooth gold and glass substrates. With the help of the obtained topography AFM images, it was shown that the micellar structures are preserved on gold substrates after evaporation of the solvent despite the new set of stresses due mainly to capillary forces and dehydration. The influence of the substrate on the resulting micellar morphology observed in air was investigated for these two materials: cylindrical micelles were evidenced as loosely adherent on gold surface in the presence of parachlorobenzoate (PCB) and identical, geometrically speaking, to those known to exist in aqueous solutions. In this situation, topographic AFM images allowed us to determine accurately their geometrical characteristics such as diameter and length in the nanometer range. On the other hand, AFM images obtained in air on glass surfaces revealed micellar structures that are different from those existing in the bulk of the solution. Indeed, bilayer-type micelles with a thickness close to twice the surfactant monomer expected length were observed, indicating that the well-established and strong influence of glass on micelle geometry at the glass/solution interface is maintained after evaporation of water. These results have been analyzed on the basis of positive charge of gold deduced from electrochemical impedance spectroscopy (EIS) and Raman spectroscopy measurements on one hand and of the negative charge of glass on the other hand. Although these results appeal to new theoretical considerations dealing with dynamics of evaporation of micellar solution drops and/or with counterion contributions to macromolecular interactions in aqueous solutions and in air, this new AFM imaging method appears to be the more adequate one to image and measure the micelles formed in the presence of water.
由阳离子表面活性剂十八烷基三甲基铵(OTA+)或十六烷基三甲基铵(CTA+)与对氯苯甲酸根(PCB)抗衡离子在水溶液中制备的圆柱形胶束,在水蒸发后,通过敲击模式原子力显微镜(TM-AFM)成功成像在非常光滑的金和玻璃基板上。借助获得的形貌原子力显微镜图像表明,尽管由于主要是毛细作用力和脱水产生了一组新的应力,但溶剂蒸发后胶束结构仍保留在金基板上。针对这两种材料,研究了基板对在空气中观察到的所得胶束形态的影响:在对氯苯甲酸根(PCB)存在的情况下,圆柱形胶束被证明松散地附着在金表面,并且从几何角度而言与已知存在于水溶液中的那些胶束相同。在这种情况下,形貌原子力显微镜图像使我们能够准确确定它们在纳米范围内的几何特征,例如直径和长度。另一方面,在空气中玻璃表面获得的原子力显微镜图像显示出与溶液本体中存在的胶束结构不同的胶束结构。实际上,观察到厚度接近表面活性剂单体预期长度两倍的双层型胶束,这表明在水蒸发后,玻璃在玻璃/溶液界面处对胶束几何形状已确立的强烈影响得以保持。一方面根据电化学阻抗谱(EIS)和拉曼光谱测量推断出的金的正电荷,另一方面根据玻璃的负电荷,对这些结果进行了分析。尽管这些结果引发了关于胶束溶液滴蒸发动力学和/或抗衡离子对水溶液和空气中大分子相互作用贡献的新理论思考,但这种新的原子力显微镜成像方法似乎是对存在水时形成的胶束进行成像和测量的更合适方法。