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Molecular resolution in dynamic force microscopy: topography and dissipation for weakly interacting systems

机译:动态力显微镜中的分子分辨率:弱相互作用系统的形貌和耗散

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Dynamic force microscopy can be used to study the growth of organic molecules on insulating substrates. The organic molecule 3,4,9,10- perylenetetracarboxylic- dianhydride ( PTCDA) exhibits Volmer - Weber growth on KBr( 001). While large areas are uncovered, some PTCDA crystallites of different heights, from two monolayers ( ML) up to 20 - 30 ML, can be seen, even at low coverages. On the topmost layer of the crystallites, single molecules can be resolved. Such a molecular contrast does not only show in topography but also in the dissipation signal. Here, the signal strongly depends on the frequency shift, i.e., the minimum distance between tip and sample. At large frequency shifts, the dissipation is enhanced between the molecules, if the frequency shift is lower, a shift of 0.2 nm between the peaks in topography and dissipation channel occurs. We propose a model that takes the crystalline growth of PTCDA into account, the shift between both signals being an effect of the two topmost layers of molecules.
机译:动态力显微镜可用于研究绝缘基板上有机分子的生长。有机分子3,4,9,10- per四羧酸二酐(PTCDA)在KBr(001)上表现出Volmer-Weber生长。当发现大面积区域时,即使在低覆盖率下,也可以看到一些高度不同的PTCDA微晶,从两个单层(ML)到20-30 ML。在微晶的最顶层,可以解析单个分子。这种分子对比不仅在形貌上显示,而且在耗散信号上也显示。在此,信号在很大程度上取决于频移,即尖端与样本之间的最小距离。在大的频移下,分子之间的耗散会增强,如果频移较低,则会在形貌的峰值和耗散通道之间​​发生0.2 nm的偏移。我们提出了一个模型,该模型考虑了PTCDA的晶体生长,两个信号之间的偏移是两个最顶层分子的作用。

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