Department of Physics and Astronomy, University College London , Gower Street, London WC1E 6BT, United Kingdom.
ACS Nano. 2014 May 27;8(5):5339-51. doi: 10.1021/nn501785q. Epub 2014 May 12.
We demonstrate that using metallic tips for noncontact atomic force microscopy (NC-AFM) imaging at relatively large (>0.5 nm) tip-surface separations provides a reliable method for studying molecules on insulating surfaces with chemical resolution and greatly reduces the complexity of interpreting experimental data. The experimental NC-AFM imaging and theoretical simulations were carried out for the NiO(001) surface as well as adsorbed CO and Co-Salen molecules using Cr-coated Si tips. The experimental results and density functional theory calculations confirm that metallic tips possess a permanent electric dipole moment with its positive end oriented toward the sample. By analyzing the experimental data, we could directly determine the dipole moment of the Cr-coated tip. A model representing the metallic tip as a point dipole is described and shown to produce NC-AFM images of individual CO molecules adsorbed onto NiO(001) in good quantitative agreement with experimental results. Finally, we discuss methods for characterizing the structure of metal-coated tips and the application of these tips to imaging dipoles of large adsorbed molecules.
我们证明,在相对较大的(>0.5nm)针尖-表面分离距离下使用金属针尖进行非接触原子力显微镜(NC-AFM)成像,为在具有化学分辨率的绝缘表面上研究分子提供了一种可靠的方法,并大大降低了解释实验数据的复杂性。使用 Cr 涂层的 Si 针尖进行了实验性 NC-AFM 成像和理论模拟,用于 NiO(001)表面以及吸附的 CO 和 Co-Salen 分子。实验结果和密度泛函理论计算证实,金属针尖具有永久电偶极矩,其正端指向样品。通过分析实验数据,我们可以直接确定 Cr 涂层尖端的偶极矩。描述了一个将金属尖端表示为点偶极子的模型,并显示出与实验结果非常吻合的吸附在 NiO(001)上的单个 CO 分子的 NC-AFM 图像。最后,我们讨论了表征金属涂层尖端结构的方法以及这些尖端在成像大吸附分子偶极子中的应用。