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Structure and composition of binary monolayers self-assembled from sodium 2-mercaptoetanosulfonate and mercaptoundecanol mixed solutions on silver and gold supports

机译:由2-巯基乙磺酸钠和巯基十一烷醇混合溶液在银和金载体上自组装的二元单层的结构和组成

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摘要

Voltammetric reductive desorption, scanning tunneling microscopy (STM) and surface-enhanced Raman scattering (SERS) were used to determine the composition and structure of mixed, two-component monolayers of sodium 2-mercaptoetanosulfonate (MES) and mercaptoundecanol (MUL) on silver and gold supports. Monolayers were prepared by self assembling from ethanolic solutions of varying composition. Preferred adsorption of MUL was found in the electrochemical experiments on Au(111). The presence of two well-separated reductive desorption peaks in the voltammograms of the mixed monolayers on Au(111) indicated the existence of MES-rich and MUL-rich phases in a wide range of solution compositions. STM imaging confirmed formation of a few-nanometer-wide thiol domains for x_(MES) greater than 0.5 in the solution used for SAMs preparation. On the contrary, SERS experiments pointed at dominant adsorption of MES on rough Ag and Au substrates. Nearly exclusive adsorption of the MES for x_(MES) greater than 0.5 was observed on the rough Ag surface.
机译:伏安还原解吸,扫描隧道显微镜(STM)和表面增强拉曼散射(SERS)用于测定银和银上的2-巯基乙磺酸钠(MES)和巯基癸醇(MUL)的混合,两组分单层混合膜的组成和结构。黄金支持。通过自组装从不同组成的乙醇溶液中制备单分子膜。在Au(111)的电化学实验中发现了MUL的优选吸附。在Au(111)上的混合单分子层的伏安图中,两个完全分离的还原性解吸峰的存在表明,在各种溶液组成中都存在MES富相和MUL富相。 STM成像证实用于SAMs制备的溶液中x_(MES)大于0.5的几纳米宽的巯基结构域的形成。相反,SERS实验指出MES在粗糙的Ag和Au基底上的主要吸附。在粗糙的Ag表面上观察到几乎大于0.5的x_(MES)对MES的吸附。

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