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铜(111)表面上通过氢键连接的均苯三酸网络揭示了基本化学性质是如何在高分辨率原子力显微镜(HR-AFM)图像中得以体现的。

Hydrogen bonded trimesic acid networks on Cu(111) reveal how basic chemical properties are imprinted in HR-AFM images.

作者信息

Zahl Percy, Yakutovich Aliaksandr V, Ventura-Macías Emiliano, Carracedo-Cosme Jaime, Romero-Muñiz Carlos, Pou Pablo, Sadowski Jerzy T, Hybertsen Mark S, Pérez Rubén

机构信息

Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, NY 11973-5000, USA.

Swiss Federal Laboratories for Materials Science and Technology (Empa), nanotech@surfaces laboratory, CH-8600 Dübendorf, Switzerland.

出版信息

Nanoscale. 2021 Nov 18;13(44):18473-18482. doi: 10.1039/d1nr04471k.

Abstract

High resolution non-contact atomic force microscopy measurements characterize assemblies of trimesic acid molecules on Cu(111) and the link group interactions, providing the first fingerprints utilizing CO-based probes for this widely studied paradigm for hydrogen bond driven molecular self assembly. The enhanced submolecular resolution offered by this technique uniquely reveals key aspects of the competing interactions. Accurate comparison between full-density-based modeled images and experiment allows to identify key structural elements in the assembly in terms of the electron-withdrawing character of the carboxylic groups, interactions of those groups with Cu atoms in the surface, and the valence electron density in the intermolecular region of the hydrogen bonds. This study of trimesic acid assemblies on Cu(111) combining high resolution atomic force microscopy measurements with theory and simulation forges clear connections between fundamental chemical properties of molecules and key features imprinted in force images with submolecular resolution.

摘要

高分辨率非接触原子力显微镜测量表征了均苯三甲酸分子在Cu(111)上的组装以及连接基团相互作用,利用基于CO的探针为这种广泛研究的氢键驱动分子自组装范例提供了首个指纹图谱。该技术提供的增强的亚分子分辨率独特地揭示了竞争相互作用的关键方面。基于全密度的建模图像与实验之间的准确比较,使得能够根据羧基的吸电子特性、这些基团与表面Cu原子的相互作用以及氢键分子间区域的价电子密度,识别组装体中的关键结构元素。这项关于均苯三甲酸在Cu(111)上组装的研究,将高分辨率原子力显微镜测量与理论和模拟相结合,在分子的基本化学性质与具有亚分子分辨率的力图像中印记的关键特征之间建立了清晰的联系。

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