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Monitoring Morphological Changes in 2D Mono layer Semiconductors Using Atom-Thick Plasmonic Nanocavities

机译:使用原子厚的等离子体纳米腔监测二维单层半导体的形态变化

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Nanometer-sized gaps between plasmonically coupled adjacent metal nanoparticles enclose extremely localized optical fields, which are strongly enhanced. This enables the dynamic investigation of nanoscopic amounts of material in the gap using optical interrogation. Here we use impinging light to directly tune the optical resonances inside the plasmonic nanocavity formed between single gold nanoparticles and a gold surface, filled with only yoctograms of semiconductor. The gold faces are separated by either monolayers of molybdenum disulfide (MoS2) or two-unit-cell thick cadmium selenide (CdSe) nanoplatelets. This extreme confinement produces modes with 100-fold compressed wavelength, which are exquisitely sensitive to morphology. Infrared scattering spectroscopy reveals how such nanoparticle-on-mirror modes directly trace atomic-scale changes in real time. Instabilities observed in the facets are crucial for applications such as heat-assisted magnetic recording that demand long-lifetime nanoscale plasmonic structures, but the spectral sensitivity also allows directly tracking photochemical reactions in these 2-dimensional solids.
机译:等离子体耦合的相邻金属纳米粒子之间的纳米级间隙围住了极强的局部电场。这使得能够使用光学询问来动态研究间隙中材料的纳米量。在这里,我们使用入射光直接调整在单个金纳米粒子和仅填充了八边形半导体图的金表面之间形成的等离子纳米腔内部的光学共振。金面被二硫化钼(MoS2)的单层或两单元厚的硒化镉(CdSe)纳米片分开。这种极端的限制产生了具有100倍压缩波长的模式,这些模式对形态非常敏感。红外散射光谱揭示了这种纳米镜面上的模式如何直接实时实时跟踪原子尺度的变化。刻面中观察到的不稳定性对于诸如热辅助磁记录之类的应用至关重要,例如需要长寿命的纳米级等离激元结构的热辅助磁记录,但是光谱灵敏度还可以直接跟踪这些二维固体中的光化学反应。

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