Chutora Taras, de la Torre Bruno, Mutombo Pingo, Hellerstedt Jack, Kopeček Jaromír, Jelínek Pavel, Švec Martin
Regional Centre of Advanced Technologies and Materials, Department of Physical Chemistry, Faculty of Science, Palacký University, Šlechtitelů 27, 78371 Olomouc, Czech Republic.
Institute of Physics of the Czech Academy of Sciences, Cukrovarnická 10, 162 00 Prague, Czech Republic.
Beilstein J Nanotechnol. 2019 Jan 30;10:315-321. doi: 10.3762/bjnano.10.30. eCollection 2019.
We investigate the possibility of functionalizing Au tips by NO molecules deposited on a Au(111) surface and their further use for imaging with submolecular resolution. First, we characterize the adsorption of the NO species on Au(111) by means of atomic force microscopy with CO-functionalized tips and density functional theory (DFT) simulations. Subsequently we devise a method of attaching a single NO to a metal tip apex and benchmark its high-resolution imaging and spectroscopic capabilities using FePc molecules. Our results demonstrate the feasibility of high-resolution imaging. However, we find an inherent asymmetry of the NO probe-particle adsorption on the tip apex, in contrast to a CO tip reference. These findings are consistent with DFT calculations of the NO- and CO tip apexes.
我们研究了通过沉积在Au(111)表面的NO分子对金尖端进行功能化的可能性,以及它们进一步用于亚分子分辨率成像的用途。首先,我们借助具有CO功能化尖端的原子力显微镜和密度泛函理论(DFT)模拟来表征NO物种在Au(111)上的吸附。随后,我们设计了一种将单个NO附着到金属尖端顶点的方法,并使用FePc分子对其高分辨率成像和光谱能力进行了基准测试。我们的结果证明了高分辨率成像的可行性。然而,与CO尖端参考相比,我们发现NO探针-粒子在尖端顶点的吸附存在固有的不对称性。这些发现与NO和CO尖端顶点的DFT计算结果一致。