اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدChiroptical response of a single plasmonic nanohelix
134
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We investigate the chiroptical response of a single plasmonic nanohelix interacting with a weakly-focused circularly-polarized Gaussian beam. The optical scattering at the fundamental resonance is characterized experimentally, and the chiral behavior of the nanohelix is explained based on a multipole analysis. The angularly resolved emission of the excited nanohelix is verified experimentally and it validates the theoretical results. Further, we study the first higher-order resonance and explain the formation of chiral dipoles in both cases.
قيم البحث
اقرأ أيضاً
Nanophotonic chiral antennas exhibit orders of magnitude higher circular dichroism (CD) compared to molecular systems. Merging magnetism and structural chirality at the nanometric level allows for the efficient magnetic control of the dichroic respon
se, bringing exciting new prospects to active nanophotonic devices and magnetochirality. Here we devise macroscale enantiomeric magnetophotonic metasurfaces of plasmon and ferromagnetic spiral antennas. Mixed 2D- and 3D- chiral nanoantennas induce large CD response, where we identify reciprocal and non-reciprocal contributions. The simultaneous chiroptical and magneto-optical response in a wide spectral range with these metasurfaces delivers an attractive platform for the study of magnetochirality at the nanoscale. Exploring further this type of magnetophotonic metasurfaces allows the realization of high-sensitivity chiral sensors and prompts the design of novel macroscopic optical devices operating with polarized light.
We report a measurement on the temporal response of a plasmonic antenna at the femtosecond time scale. The antenna consists of a square array of nanometer-size gold rods. We find that the far-field dispersion of light reflected from the plasmonic ant
enna is less than that of a 1.2 mm thick glass slide. Assuming a simple oscillating dipole model this implies that the near-field of the antenna may be used as an electron switch that responds faster than 20 fs. Alternatively, ultrafast electron diffraction may be used to investigate the near-field dynamics of the plasmonic antenna.
The nonlinear optical response of materials to exciting light is enhanced by resonances between the incident laser frequencies and the energy levels of the excited material. Traditionally, in molecular nonlinear spectroscopy one tunes the input laser
frequencies to the molecular energy levels for highly enhanced doubly or triply resonant interactions. With metasurfaces the situation is different, and by proper design of the nanostructures, one may tune the material energy levels to match the incoming laser frequencies. Here we use multi-parameter genetic algorithm methodologies to optimize the nonlinear Four Wave Mixing response, and show that the intuitive conventional approach of trying to match the transmission spectrum to the relevant laser frequencies indeed leads to strong enhancement, but not necessarily to the optimal design. We demonstrate, experimentally and by direct nonlinear field calculations, that the near field mode distribution and spatial modes overlap are the dominant factor for optimized design.
Plasmonic nanoantennas allow for enhancing the spontaneous emission, altering the emission polarization, and shaping the radiation pattern of quantum emitters. A critical challenge for the experimental realizations is positioning a single emitter int
o the hotspot of a plasmonic antenna with nanoscale accuracy. We demonstrate a dynamic light-matter interaction nanosystem enabled by the DNA origami technique. A single fluorophore molecule can autonomously and unidirectionally walk into the hotspot of a plasmonic nanoantenna along a designated origami track. Successive fluorescence intensity increase and lifetime reduction are in situ monitored using single-molecule fluorescence spectroscopy, while the fluorophore walker gradually approaches and eventually enters the plasmonic hotspot. Our scheme offers a dynamic platform, which can be used to develop functional materials, investigate intriguing light-matter interaction phenomena, and serve as prototype system for examining theoretical models.
Nanofabrication of photonic components based on dielectric-loaded surface plasmon-polariton waveguides (DLSPPWs) excited by single nitrogen vacancy (NV) centers in nanodiamonds is demonstrated. DLSPPW circuits are built around NV containing nanodiamo
nds, which are certified to be single-photon emitters, using electron-beam lithography of hydrogen silsesquioxane (HSQ) resist on silver-coated silicon substrates. A propagation length of ~20 {mu}m for the NV single-photon emission is measured with DLSPPWs. A 5-fold enhancement in the total decay rate and up to 63% coupling efficiency to the DLSPPW mode is achieved, indicating significant mode confinement. Finally, we demonstrate routing of single plasmons with DLSPPW-based directional cou-plers, revealing the potential of our approach for on-chip realization of quantum-optical networks.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
