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利用基于音叉的非接触原子力显微镜对 C60 分子进行高分辨率成像。

High-resolution imaging of C60 molecules using tuning-fork-based non-contact atomic force microscopy.

机构信息

Department of Physics, University of Basel, Basel, Switzerland.

出版信息

J Phys Condens Matter. 2012 Feb 29;24(8):084005. doi: 10.1088/0953-8984/24/8/084005. Epub 2012 Feb 7.

DOI:10.1088/0953-8984/24/8/084005
PMID:22310075
Abstract

Recent advances in non-contact atomic force microscopy (nc-AFM) have led to the possibility of achieving unprecedented resolution within molecular structures, accomplished by probing short-range repulsive interaction forces. Here we investigate C(60) molecules adsorbed on KBr(111) and Cu(111) by tuning-fork-based nc-AFM. First, measurements of C(60) deposited on KBr(001) were conducted in cryogenic conditions revealing highly resolved nc-AFM images of the self-assembly. Using constant-frequency shift mode as well as three-dimensional spectroscopic measurements, we observe that the relatively weak molecule-substrate interaction generally leads to the disruption of molecular assembled structures when the tip is probing the short-range force regime. This particular issue hindered us in resolving the chemical structure of this molecule on the KBr surface. To obtain a better anchoring of C(60) molecules, nc-AFM measurements were performed on Cu(111). Sub-molecular resolutions within the molecules was achieved which allowed a direct and unambiguous visualization of their orientations on the supporting substrate. Furthermore, three-dimensional spectroscopic measurements of simultaneous force and current have been performed above the single molecules giving information of the C(60) molecular orientation as well as its local conductivity. We further discuss the different imaging modes in nc-AFM such as constant-frequency shift nc-AFM, constant-height nc-AFM and constant-current nc-AFM as well as three-dimensional spectroscopic measurement (3D-DFS) employed to achieve such resolution at the sub-molecular scale.

摘要

近年来,非接触原子力显微镜(nc-AFM)技术的发展使得在分子结构中实现前所未有的分辨率成为可能,这是通过探测短程排斥相互作用力来实现的。在这里,我们通过基于音叉的 nc-AFM 研究了吸附在 KBr(111)和 Cu(111)上的 C(60)分子。首先,我们在低温条件下对沉积在 KBr(001)上的 C(60)进行了测量,揭示了自组装的高分辨率 nc-AFM 图像。通过使用恒频移模式和三维光谱测量,我们观察到相对较弱的分子-基底相互作用通常会导致当针尖探测短程力范围时分子组装结构的破坏。这个特殊的问题阻碍了我们在 KBr 表面上解析这个分子的化学结构。为了获得更好的 C(60)分子固定,我们在 Cu(111)上进行了 nc-AFM 测量。在分子内实现了亚分子分辨率,这允许直接和明确地可视化它们在支撑基底上的取向。此外,在单个分子上方进行了同时测量力和电流的三维光谱测量,提供了 C(60)分子取向及其局部电导率的信息。我们进一步讨论了 nc-AFM 中的不同成像模式,如恒频移 nc-AFM、恒高 nc-AFM 和恒流 nc-AFM 以及用于在亚分子尺度实现这种分辨率的三维光谱测量(3D-DFS)。

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