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Understanding the near-field electromagnetic interactions that produce optical orbital angular momentum (OAM) is crucial for integrating twisted light into nanotechnology. Here, we examine the cathodoluminescence (CL) of plasmonic vortices carrying OAM generated in spiral nanostructures. The nanospiral geometry defines a photonic local density of states that is sampled by the electron probe in a scanning transmission electron microscope (STEM), thus accessing the optical response of the plasmonic vortex with high spatial and spectral resolution. We map the full spectral dispersion of the plasmonic vortex in spiral structures designed to yield increasing topological charge. Additionally, we fabricate nested nanospirals and demonstrate that OAM from one nanospiral can be coupled to the nested nanospiral, resulting in enhanced luminescence in concentric spirals of like handedness with respect to concentric spirals of opposite handedness. The results illustrate the potential for generating and coupling plasmonic vortices in chiral nanostructures for sensitive detection and manipulation of optical OAM.

Hybrid material systems are a promising approach for extending the capabilities of silicon photonics. Given the weak electro‐optic and thermo‐optic effects in silicon, there is intense interest in integrating an ultrafast‐switching phase‐change material with a large refractive index contrast into the waveguide, such as vanadium dioxide (VO₂). It is well established that the phase transition in VO₂thin films can be triggered by ultrafast, 800 nm laser pulses, and that pump‐laser fluence is a critical determinant of the recovery time of thin films irradiated by femtosecond pulses. However, thin‐film experiments are not reliable guides to a VO₂:Si system for all‐optical, on‐chip switching because of the differences in VO₂optical constants in the telecommunication band, and the complex sample geometry and alignment issues in a waveguide geometry. This paper reports the first demonstration that the reversible, ultrafast photoinduced phase transition in VO₂can achieve sub‐picosecond response when small VO₂volumes are integrated into a silicon waveguide as the active element. The result suggests that VO₂can be pursued as a strong candidate for waveguide switching with sub‐picosecond on‐off times.

Zinc oxide (ZnO) nanowires are widely studied for use in ultraviolet optoelectronic devices, such as nanolasers and sensors. Nanowires (NWs) with an MgO shell exhibit enhanced band‐edge photoluminescence (PL), a result previously attributed to passivation of ZnO defects. However, we find that processing the ZnO NWs under low oxygen partial pressure leads to an MgO‐thickness‐dependent PL enhancement owing to the formation of optical cavity modes. Conversely, processing under higher oxygen partial pressure leads to NWs that support neither mode formation nor band‐edge PL enhancement. High‐resolution electron microscopy and density‐functional calculations implicate the ZnOm‐plane surface morphology as the key determinant of core‐shell structure and cavity‐mode optics. A ZnO surface with atomic steps along them‐plane in thec‐axis direction stimulates the growth of a smooth MgO shell that supports guided‐wave optical modes and enhanced UV PL. On the other hand, a smoother ZnO surface leads to nucleation of a rough cladding layer which supports neither enhanced UV PL nor optical cavity modes. Finite‐element analysis shows a clear correlation between allowed Fabry‐Perot and whispering gallery modes and enhanced UV‐PL. These results point the way to fabricating ZnO/MgO core‐shell nanowires for more efficient UV nanolasers, scintillators, and sensors.