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利用非线性光散射对水纳米液滴界面的自组装进行量化

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

作者信息

Smolentsev N, Roke S

机构信息

Laboratory for Fundamental BioPhotonics (LBP), Institute of Bioengineering (IBI), and Institute of Materials Science (IMX), School of Engineering (STI), and Lausanne Centre for Ultrafast Science (LACUS), École Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland.

出版信息

Langmuir. 2020 Aug 11;36(31):9317-9322. doi: 10.1021/acs.langmuir.0c01887. Epub 2020 Jul 27.

Abstract

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.

摘要

水的微滴和纳米滴界面驱动着环境、医学、催化、生物和化学双相过程。液滴界面结构和静电作用在很大程度上决定了这些过程的反应活性和效率。液滴的界面性质难以捉摸,通常是从体相测量中推断出来的,因此远非精确。在这里,我们使用角分辨偏振二次谐波散射来量化非极性液体中纳米级水滴的水界面有序性和静电表面电势。我们还提出了一种确定疏水相中自由电荷数量的方法,其灵敏度比电导率测量高3个数量级。通过研究AOT表面活性剂吸附引起的结构和表面静电变化,我们发现氢键和静电作用都强烈依赖于表面活性剂浓度。高于临界胶束浓度时,界面介导胶束自组装。

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