No Arabic abstract
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 into 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.
Guided-wave plasmonic circuits are promising platforms for sensing, interconnection, and quantum applications in the sub-diffraction regime. Nonetheless, the loss-confinement trade-off remains a collective bottleneck for plasmonic-enhanced optical processes. Here, we report a unique plasmonic waveguide that can alleviate such trade-off and improve the efficiencies of plasmonic-based emission, light-matter-interaction, and detection simultaneously. Through different bias configurations, record experimental attributes such as normalized Purcell factor approaching 10^4, 10-dB amplitude modulation with <1 dB insertion loss and fJ-level switching energy, and photodetection sensitivity and internal quantum efficiency of -54 dBm and 6.4 % respectively can be realized within the same amorphous-based plasmonic structure. The ability to support multiple optoelectronic phenomena while providing performance gains over existing plasmonic and dielectric counterparts offers a clear path towards reconfigurable, monolithic plasmonic circuits.
Fabricating nanocavities in which optically-active single quantum emitters are precisely positioned, is crucial for building nanophotonic devices. Here we show that self-assembly based on robust DNA-origami constructs can precisely position single molecules laterally within sub-5nm gaps between plasmonic substrates that support intense optical confinement. By placing single-molecules at the center of a nanocavity, we show modification of the plasmon cavity resonance before and after bleaching the chromophore, and obtain enhancements of $geq4times10^3$ with high quantum yield ($geq50$%). By varying the lateral position of the molecule in the gap, we directly map the spatial profile of the local density of optical states with a resolution of $pm1.5$ nm. Our approach introduces a straightforward non-invasive way to measure and quantify confined optical modes on the nanoscale.
We propose a plasmonic ellipse resonator possessing hybrid modes based on metal-insulator-metal (MIM) waveguide system. Specially, this nanocavity has hybrid characteristic of rectangle and disk resonator, therefore supporting both Fabry-Perot modes (FPMs) and whispering-gallery modes (WGMs). Besides, by changing the length of major and minor radius of the ellipse, the resonant wavelengths of FPMs and WGMs can be independently tuned and close to each other, thus constructing a plasmon-induced transparency (PIT) - like spectrum profile. Benefitting from this, a dual-band slow light is achieved with one single resonator. Furthermore, this component can also act as a multi-band color filter and refractive index sensor. We believe such multi-mode resonator with ultra-small footprint will play an important role in more compact on-chip optical circuits in the future.
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.
In the quest to enhance light-matter interactions and miniaturize photonics devices, it is crucial to create a strong field enhancement with lower material losses. Here we combine a plasmonic Fano resonance supported by the silver cluster and anapole states realized by the silicon disk to create a larger field enhancement with less loss through a strong coupling effect. Besides, by varying the gap size we find that the resonances wavelength and the Rabi-splitting can be tuned over a wide range of wavelength, which can achieve a giant splitting energy over 300 meV. We further demonstrate that it is the interference of magnetic currents loops which induces the strong coupling. Due to the strong coupling, the hybrid antenna can provide both larger decay rate and radiative decay rate, which makes it promising for high-performance miniaturized optical devices.