Self-Assembly at Water Nanodroplet Interfaces Quantified with Nonlinear Light Scattering

被引:13
|
作者
Smolentsev, N. [1 ,2 ,3 ]
Roke, S. [1 ,2 ,3 ]
机构
[1] Ecole Polytech Fed Lausanne EPFL, Inst Bioengn IBI, Lab Fundamental BioPhoton LBP, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne EPFL, Inst Mat Sci IMX, Sch Engn STI, CH-1015 Lausanne, Switzerland
[3] Ecole Polytech Fed Lausanne EPFL, Lausanne Ctr Ultrafast Sci LACUS, CH-1015 Lausanne, Switzerland
基金
欧洲研究理事会;
关键词
2ND-HARMONIC GENERATION; CONFINED WATER; SURFACE; AOT; DROPLETS; PARTICLES; HYDRATION; DYNAMICS;
D O I
10.1021/acs.langmuir.0c01887
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interfaces of water micro- and nanodroplets drive environmental, medical, catalytic, biological, and chemical biphasic processes. The interfacial droplet structure and electrostatics greatly determine the reactivity and efficiency of these processes. Droplet interfacial properties are elusive and generally inferred from bulk measurements and are therefore anything but exact. Here, we quantify the interfacial ordering of water and the electrostatic surface potential of nanoscale water droplets in an apolar liquid using angle-resolved polarimetric second-harmonic scattering. We also present a method to determine the amount of free charges in the hydrophobic phase, reaching a sensitivity that is 3 orders of magnitude better than conductivity measurements. Investigating the structural and surface electrostatic changes induced by AOT surfactant adsorption, we find that both the hydrogen bonding as well as the electrostatics strongly depend on the surfactant concentration. Above the critical micelle concentration, the interface mediates micelle self-assembly.
引用
收藏
页码:9317 / 9322
页数:6
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