AMPEL, ‡Department of Chemistry, University of British Columbia , Vancouver, British Columbia V6T 1Z1, Canada.
J Am Chem Soc. 2015 Jan 14;137(1):276-88. doi: 10.1021/ja5104475. Epub 2014 Dec 24.
The use of a single crystal gold bead electrode is demonstrated for characterization of self-assembled monolayers (SAM)s formed on the bead surface expressing a complete set of face centered cubic (fcc) surface structures represented by a stereographic projection. Simultaneous analysis of many crystallographic orientations was accomplished through the use of an in situ fluorescence microscopic imaging technique coupled with electrochemical measurements. SAMs were prepared from different classes of molecules, which were modified with a fluorescent tag enabling characterization of the influence of electrical potential and a direct comparison of the influence of surface structure on SAMs adsorbed onto low index, vicinal and chiral surfaces. The assembly of alkylthiol, Aib peptide and DNA SAMs are studied as a function of the electrical potential of the interface revealing how the organization of these SAMs depend on the surface crystallographic orientation, all in one measurement. This approach allows for a simultaneous determination of SAMs assembled onto an electrode surface onto which the whole fcc stereographic triangle can be mapped, revealing the influence of intermolecular interactions as well as the atomic arrangement of the substrate. Moreover, this method enables study of the influence of the Au surface atom arrangement on SAMs that were created and analyzed, both under identical conditions, something that can be challenging for the typical studies of this kind using individual gold single crystal electrodes. Also demonstrated is the analysis of a SAM containing two components prepared using thiol exchange. The two component SAM shows remarkable differences in the surface coverage, which strongly depends on the surface crystallography enabling estimates of the thiol exchange energetics. In addition, these electrode surfaces enable studies of molecular adsorption onto the symmetry related chiral surfaces since more than one stereographic triangle can be imaged at the same time. The ability to observe a SAM modified surface that contains many complete fcc stereographic triangles will facilitate the study of the single and multicomponent SAMs, identifying interesting surfaces for further analysis.
本文展示了如何使用单晶金珠电极来表征在金珠表面形成的自组装单层(SAM),这些 SAM 表面表达了由立体投影表示的完整面心立方(fcc)表面结构。通过使用原位荧光显微镜成像技术与电化学测量相结合,实现了对许多晶体取向的同时分析。SAM 是由不同类别的分子制备的,这些分子用荧光标记进行了修饰,从而能够对电势能的影响进行表征,并对吸附在低指数、近晶和手性表面上的 SAM 的表面结构的影响进行直接比较。研究了烷基硫醇、Aib 肽和 DNA SAM 的组装作为界面电势能的函数,揭示了这些 SAM 的组织如何依赖于表面晶体取向,所有这些都在一次测量中完成。这种方法允许同时确定组装到电极表面上的 SAM,该电极表面可以映射整个 fcc 立体三角,从而揭示分子间相互作用以及基底原子排列对 SAM 的影响。此外,这种方法还可以研究在相同条件下创建和分析的 SAM 中 Au 表面原子排列的影响,这对于使用单个金单晶电极进行的典型此类研究来说是具有挑战性的。本文还展示了使用硫醇交换制备的含有两种成分的 SAM 的分析。该双组分 SAM 显示出在表面覆盖率上的显著差异,这强烈依赖于表面晶体学,从而能够估计硫醇交换的能量学。此外,这些电极表面还能够研究分子吸附到对称相关的手性表面上,因为可以同时对多个立体三角进行成像。观察包含许多完整 fcc 立体三角的 SAM 修饰表面的能力将有助于对单组分和多组分 SAM 的研究,从而确定用于进一步分析的有趣表面。