Laboratory for fundamental BioPhotonics (LBP), Institute of Bioengineering (IBI), School of Engineering, École Polytechnique Fédérale de Lausanne (EPFL) , 1015 Lausanne, Switzerland.
J Am Chem Soc. 2013 Dec 26;135(51):19330-5. doi: 10.1021/ja4102858. Epub 2013 Dec 13.
The molecular ionic surface structure and charge of the electric double layer around a nanodroplet and its structural change induced by hydrophobic effects are measured using vibrational coherent surface scattering spectroscopy, second harmonic scattering, and electrokinetic mobility measurements. Tetraalkylammonium chloride salts were added to negatively charged nanoscopic oil droplets in water. When we vary the alkyl chain length of the cation from CH3 to C4H10, both the size of the cation and its hydrophobic interaction are increased. We find that tetramethylammonium ions change the electrokinetic potential and the water structure but do not detectably adsorb to the interface. Tetrapropylammonium and tetrabutylammonium ions clearly adsorb to the interface. The corresponding (Stern) layer appears to be a mixed monolayer of anions and cations. An estimate of the amount of cations in the Stern layer is also made.
使用振动相干表面散射光谱、二次谐波散射和电动迁移率测量,测量了纳米液滴周围双电层的分子离子表面结构和电荷,以及疏水效应引起的结构变化。向带负电的纳米油滴在水中添加了四烷基氯化铵盐。当我们将阳离子的烷基链长度从 CH3 变为 C4H10 时,阳离子的大小及其疏水相互作用都增加了。我们发现四甲基铵离子会改变电动电势和水的结构,但不会明显吸附到界面上。四丙基铵和四丁基铵离子则明显吸附到界面上。相应的(斯特恩)层似乎是阴离子和阳离子的混合单层。还对斯特恩层中阳离子的数量进行了估计。