Imaging and steering an optical wireless nanoantenna link.

Optical nanoantennas tailor the transmission and reception of optical signals. Owing to their capacity to control the direction and angular distribution of optical radiation over a broad spectral range, nanoantennas are promising components for optical communication in nanocircuits. Here we measure wireless optical power transfer between plasmonic nanoantennas in the far-field and demonstrate changeable signal routing to different nanoscopic receivers via beamsteering. We image the radiation pattern of single-optical nanoantennas using a photoluminescence technique, which allows mapping of the unperturbed intensity distribution around plasmonic structures. We quantify the distance dependence of the power transmission between transmitter and receiver by deterministically positioning nanoscopic fluorescent receivers around the transmitting nanoantenna. By adjusting the wavefront of the optical field incident on the transmitter, we achieve directional control of the transmitted radiation over a broad range of 29°. This enables wireless power transfer from one transmitter to different receivers.

Vibrational near-field mapping of planar and buried three-dimensional plasmonic nanostructures.

Nanoantennas confine electromagnetic fields at visible and infrared wavelengths to volumes of only a few cubic nanometres. Assessing their near-field distribution offers fundamental insight into light-matter coupling and is of special interest for applications such as radiation engineering, attomolar sensing and nonlinear optics. Most experimental approaches to measure near-fields employ either diffraction-limited far-field methods or intricate near-field scanning techniques. Here, using diffraction-unlimited far-field spectroscopy in the infrared, we directly map the intensity of the electric field close to plasmonic nanoantennas. We place a patch of probe molecules with 10 nm accuracy at different locations in the near-field of a resonant antenna and extract the molecular vibrational excitation. We map the field intensity along a dipole antenna and gap-type antennas. Moreover, this method is able to assess the near-field intensity of complex buried plasmonic structures. We demonstrate this by measuring for the first time the near-field intensity of a three-dimensional plasmonic electromagnetically induced transparency structure.

Nonreciprocal plasmonics enables giant enhancement of thin-film Faraday rotation.

Light propagation is usually reciprocal. However, a static magnetic field along the propagation direction can break the time-reversal symmetry in the presence of magneto-optical materials. The Faraday effect in magneto-optical materials rotates the polarization plane of light, and when light travels backward the polarization is further rotated. This is applied in optical isolators, which are of crucial importance in optical systems. Faraday isolators are typically bulky due to the weak Faraday effect of available magneto-optical materials. The growing research endeavour in integrated optics demands thin-film Faraday rotators and enhancement of the Faraday effect. Here, we report significant enhancement of Faraday rotation by hybridizing plasmonics with magneto-optics. By fabricating plasmonic nanostructures on laser-deposited magneto-optical thin films, Faraday rotation is enhanced by one order of magnitude in our experiment, while high transparency is maintained. We elucidate the enhanced Faraday effect by the interplay between plasmons and different photonic waveguide modes in our system.

Octave-wide photonic band gap in three-dimensional plasmonic Bragg structures and limitations of radiative coupling.

Radiative coupling between oscillators is one of the most fundamental subjects of research in optics, where particularly a Bragg-type arrangement is of interest and has already been applied to atoms and excitons in quantum wells. Here we explore this arrangement in a plasmonic structure. We observe the emergence of an octave-wide photonic band gap in the optical regime. Compared with atomic or excitonic systems, the coupling efficiency of the particle plasmons utilized here is several orders of magnitude larger and widely tunable by changing the size and geometry of the plasmonic nanowires. We are thus able to explore the regime where the coupling distance is even limited by the large radiative decay rate of the oscillators. This Bragg-stacked coupling scheme will open a new route for future plasmonic applications such as far-field coupling to quantum emitters without quenching, plasmonic cavity structures and plasmonic distributed gain schemes for spasers.

Diamond nanophotonics.

We demonstrate the coupling of single color centers in diamond to plasmonic and dielectric photonic structures to realize novel nanophotonic devices. Nanometer spatial control in the creation of single color centers in diamond is achieved by implantation of nitrogen atoms through high-aspect-ratio channels in a mica mask. Enhanced broadband single-photon emission is demonstrated by coupling nitrogen-vacancy centers to plasmonic resonators, such as metallic nanoantennas. Improved photon-collection efficiency and directed emission is demonstrated by solid immersion lenses and micropillar cavities. Thereafter, the coupling of diamond nanocrystals to the guided modes of micropillar resonators is discussed along with experimental results. Finally, we present a gas-phase-doping approach to incorporate color centers based on nickel and tungsten, in situ into diamond using microwave-plasma-enhanced chemical vapor deposition. The fabrication of silicon-vacancy centers in nanodiamonds by microwave-plasma-enhanced chemical vapor deposition is discussed in addition.

Palladium-based plasmonic perfect absorber in the visible wavelength range and its application to hydrogen sensing.

We report on the experimental realization of a palladium-based plasmonic perfect absorber at visible wavelengths and its application to hydrogen sensing. Our design exhibits a reflectance <0.5% and zero transmittance at 650 nm and the operation wavelength of the absorber can be tuned by varying its structural parameters. Exposure to hydrogen gas causes a rapid and reversible increase in reflectance on a time scale of seconds. This pronounced response introduces a novel optical hydrogen detection scheme with very high values of the relative intensity response.

Excitation and tuning of higher-order Fano resonances in plasmonic oligomer clusters.

Plasmonic oligomer clusters are assemblies of closely packed metallic nanoparticles. They provide a rich set of spectral features such as Fano lineshapes and a simultaneous tunability of the supported resonances in the optical wavelength regime. In this study, we investigate numerically and experimentally clusters of plasmonic nanoparticles that exhibit multiple Fano resonances due to the interference of one broad superradiant mode and multiple narrow subradiant modes. In particular we investigate oligomers with multiple ring modes and elongated chains of nanoparticles surrounded by one ring of nanoparticles. We show that the number of nanoparticles and their respective arrangement in the cluster strongly influence the spectral position and modulation depth of the spectral signature of the supported modes. Our study opens up the pathway to "plasmonic super molecules" that show unprecedented tunability, which renders them highly suitable for applications such as multiwavelength surface-enhanced Raman scattering.

Strong coupling of localized and surface plasmons to microcavity modes.

We strongly couple surface plasmon modes on a thin metal layer via localized plasmons of nanowires to photonic microcavity modes. In particular, we place an array of nanowires close to a mirror and position a second mirror at Bragg distance. The coupling becomes evident from an anticrossing of the resonances in the dispersion diagram. We experimentally determine the dispersion by applying external pressure to the microcavity and find excellent agreement with simulations.

Near-field dynamics of optical Yagi-Uda nanoantennas.

We present near-field measurements of optical Yagi-Uda nanoantennas that are used in receiving mode. The eigenmode imaging of amplitude and phase by apertureless scanning near-field optical microscopy allows us to investigate the dynamics of the local out-of-plane electric field components and to visualize the temporal evolution of this time-harmonic reception process. The antenna directionality manifests itself by the dependence of the local field enhancement at the feed element on the illumination direction. Simulations taking into account the substrate confirm our observation of the directionality. Our work demonstrates the possibility to characterize multielement nanoantennas by electromagnetic antenna near-field scanners.

3D optical Yagi-Uda nanoantenna array.

Future photonic circuits with the capability of high-speed data processing at optical frequencies will rely on the implementation of efficient emitters and detectors on the nanoscale. Towards this goal, bridging the size mismatch between optical radiation and subwavelength emitters or detectors by optical nanoantennas is a subject of current research in the field of plasmonics. Here we introduce an array of three-dimensional optical Yagi-Uda antennas, fabricated using top-down fabrication techniques combined with layer-by-layer processing. We show that the concepts of radiofrequency antenna arrays can be applied to the optical regime proving superior directional properties compared with a single planar optical antenna, particularly for emission and reception into the third dimension. Measuring the optical properties of the structure reveals that impinging light on the array is efficiently absorbed on the subwavelength scale because of the high directivity. Moreover, we show in simulations that combining the array with suitable feeding circuits gives rise to the prospect of beam steering at optical wavelengths.

Plasmonic oligomers: the role of individual particles in collective behavior.

We present a comprehensive experimental study of the optical properties of plasmonic oligomers. We show that both the constitution and configuration of plasmonic oligomers have a large influence on their resonant behavior, which draws a compelling analogy to molecular theory in chemistry. To elucidate the constitution influence, we vary the size of individual nanoparticles and identify the role of the target nanoparticle from the spectral change. To illustrate the configuration influence, we vary the positions and numbers of nanoparticles in a plasmonic oligomer. Additionally, we demonstrate experimentally a large spectral redshift at the transition from displaced nanoparticles to touching ones. The oligomeric design strategy opens up a rich pathway for the implementation of optimized optical properties into complex plasmonic nanostructures for specific applications.