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Atomically Resolved Graphitic Surfaces in Air by Atomic Force Microscopy

机译:原子力显微镜在空气中原子分解的石墨表面

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Imaging at the atomic scale using atomic force microscopy in biocompatible environments is an ongoing challenge. We demonstrate atomic resolution of graphite and hydrogen-intercalated graphene on SiC in air. The main challenges arise from the overall surface cleanliness and the water layers which form on almost all surfaces. To further investigate the influence of the water layers, we compare data taken with a hydrophilic bulk-silicon tip to a hydrophobic bulk-sapphire tip. While atomic resolution can be achieved with both tip materials at moderate interaction forces, there are strong differences in force versus distance spectra which relate to the water layers on the tips and samples. Imaging at very low tip-sample interaction forces results in the observation of large terraces of a naturally occurring stripe structure on the hydrogen-intercalated graphene. This structure has been previously reported on graphitic surfaces that are not covered with disordered adsorbates in ambient conditions (i.e., on graphite and bilayer graphene on SiC, but not on monolayer graphene on SiC). Both these observations indicate that hydrogenintercalated graphene is close to an ideal graphene sample in ambient environments.
机译:在生物相容性环境中使用原子力显微镜在原子尺度上成像是一项持续的挑战。我们证明了空气中SiC上的石墨和氢嵌入石墨烯的原子分辨率。主要挑战来自总体表面清洁度和几乎所有表面上形成的水层。为了进一步研究水层的影响,我们将亲水性块状硅石尖端与疏水性块状蓝宝石尖端的数据进行了比较。尽管两种尖端材料在中等相互作用力下都可以实现原子分辨率,但力与距离光谱之间存在很大差异,这与尖端和样品上的水层有关。在极低的尖端样品相互作用力下成像可观察到氢嵌入石墨烯上天然条纹结构的大台阶。先前已经报道了这种结构在环境条件下未被无序吸附物覆盖的石墨表面上(即,在SiC上的石墨和双层石墨烯上,但是在SiC上的单层石墨烯上)。这两个观察结果表明,氢嵌入的石墨烯在周围环境中接近于理想的石墨烯样品。

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