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Subdiffraction-limited far-field raman spectroscopy of single carbon nanotubes: An unenhanced approach

机译:单一碳纳米管的亚衍射极限远场拉曼光谱:未增强的方法

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摘要

We present a new approach for subdiffraction-limited far-field Raman spectroscopy of single carbon nanotubes using through-the-objective total internal reflection (TIR) excitation coupled to an atomic force microscope (AFM). By using this approach, we are able to detect spectroscopic signatures of structural changes along a single nanotube with nanometer resolution. A single multiwalled carbon nanotube is mounted on an AFM tip and imaged while tapping on the surface of a glass coverslip. As the angle of incidence of the excitation field is changed, we are able to tune the penetration depth of the evanescent field by steps as small as 2-10 nm. An increase in the ratio of the Raman D band (the disorder band) to G band (the in-plane graphitic band) of the carbon nanotube was demonstrated as the penetration depth decreased, indicating that most defects are concentrated at the end of the nanotube. We also observed frequency shifts of the G band as we changed the penetration depth. By changing the polarization of the incident beam, we are able detect the orientation and possible local curvature in the nanotubes. Coupling through-the-objective TIR with AFM is a powerful technique for studying structural and chemical properties of carbon nanotubes and can be easily extended to many other nanoscale/molecular systems.
机译:我们提出了一种新的方法,用于单碳纳米管的亚衍射极限远场拉曼光谱分析,该方法使用了通过目标全内反射(TIR)激发耦合到原子力显微镜(AFM)的方法。通过使用这种方法,我们能够检测到具有纳米分辨率的单个纳米管结构变化的光谱特征。将单个多壁碳纳米管安装在AFM尖端上,并在敲击玻璃盖玻片的表面时成像。当激发场的入射角改变时,我们能够以2-10 nm的步长来调整the逝场的穿透深度。随着穿透深度的减小,碳纳米管的拉曼D带(无序带)与G带(面内石墨带)之比增加,表明大部分缺陷集中在纳米管末端。当我们改变穿透深度时,我们还观察到了G波段的频移。通过改变入射光束的偏振,我们能够检测到纳米管的方向和可能的局部曲率。通过目标TIR与AFM耦合是研究碳纳米管结构和化学性质的一项强大技术,可以轻松扩展到许多其他纳米级/分子系统。

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