High-Q plasmonic nanowire-on-mirror resonators by atomically smooth single-crystalline silver flakes.

Plasmonic nanoparticles in close vicinity to a metal surface confine light to nanoscale volumes within the insulating gap. With gap sizes in the range of a few nanometers or below, atomic-scale dynamical phenomena within the nanogap come into reach. However, at these tiny scales, an ultra-smooth material is a crucial requirement. Here, we demonstrate large-scale (50 µm) single-crystalline silver flakes with a truly atomically smooth surface, which are an ideal platform for vertically assembled silver plasmonic nanoresonators. We investigate crystalline silver nanowires in a sub-2 nm separation to the silver surface and observe narrow plasmonic resonances with a quality factor Q of about 20. We propose a concept toward the observation of the spectral diffusion of the lowest-frequency cavity plasmon resonance and present first measurements. Our study demonstrates the benefit of using purely crystalline silver for plasmonic nanoparticle-on-mirror resonators and further paves the way toward the observation of dynamic phenomena within a nanoscale gap.

Single Molecule Nonlinearity in a Plasmonic Waveguide.

Plasmonic waveguides offer the unique possibility to confine light far below the diffraction limit. Past room temperature experiments focused on efficient generation of single waveguide plasmons by a quantum emitter. However, only the simultaneous interaction of the emitter with multiple plasmonic fields would lead to functionality in a plasmonic circuit. Here, we demonstrate the nonlinear optical interaction of a single molecule and propagating plasmons. An individual terrylene diimide (TDI) molecule is placed in the nanogap between two single-crystalline silver nanowires. A visible wavelength pump pulse and a red-shifted depletion pulse travel along the waveguide, leading to stimulated emission depletion (STED) in the observed fluorescence. The efficiency increases by up to a factor of 50 compared to far-field excitation. Our study thus demonstrates remote nonlinear four-wave mixing at a single molecule with propagating plasmons. It paves the way toward functional quantum plasmonic circuits and improved nonlinear single-molecule spectroscopy.

A Single-Crystalline Silver Plasmonic Circuit for Visible Quantum Emitters.

Plasmonic waveguides are key elements in nanophotonic devices, serving as optical interconnects between nanoscale light sources and detectors. Multimode operation in plasmonic two-wire transmission lines promises important degrees of freedom for near-field manipulation and information encoding. However, highly confined plasmon propagation along gold nanostructures is typically limited to the near-infrared region due to ohmic losses, excluding all visible quantum emitters from plasmonic circuitry. We report on the top-down fabrication of complex plasmonic nanostructures in single-crystalline silver plates. We demonstrate the controlled remote excitation of a small ensemble of fluorophores by a set of waveguide modes and the emission of the visible luminescence into the waveguide with high efficiency. This approach opens up the study of a nanoscale light-matter interaction between complex plasmonic waveguides and a large variety of quantum emitters available in the visible spectral range.

Low loss optical waveguiding in large single crystals of a thiophene-based oligomer.

Active optical waveguides based on functional small organic molecules in micro/nano regime have attracted great interest for their potential applications in high speed miniaturized photonic integrations. Here, we report on the active waveguiding properties of millimeter sized single crystals of a newly synthesized thiophene-based oligomer. These large crystals exhibit low optical loss compared to other organic nanostructures, and optical losses depend on the emission energy. Moreover, we find that the coupling of photoluminescence to waveguide modes is very efficient, typically greater than 40%. These features indicate that such perfect single crystals with a low density of defects and extremely smooth surfaces exhibit low propagation loss, which makes them good candidates for the design and the fabrication of novel organic optical fibers and lasers.

Self-Interference of Exciton Emission in Organic Single Crystals Visualized by Energy-Momentum Spectroscopy.

We employ energy-momentum spectroscopy on isolated organic single crystals with micrometer-sized dimensions. The single crystals are grown from a thiophene-based oligomer and are excellent low-loss active waveguides that support multiple guided modes. Excitation of the crystals with a diffraction-limited laser spot results in emission into guided modes as well as into quasi-discrete radiation modes. These radiation modes are mapped in energy-momentum space and give rise to dispersive interference patterns. On the basis of the known geometry of the crystals, especially the height, the characteristics of the interference maxima allow one to determine the energy dependence of two components of the anisotropic complex refractive index. Moreover, the method is suited to identify the orientation of molecules within (and around) a crystalline structure.