Alberto G. Curto

Unidirectional Emission of a Quantum Dot Coupled to a Nanoantenna

Directed Emission The atomlike features of quantum dots—the discrete energy levels and subsequent emission of light at discrete wavelengths—make them key building blocks in optoelectronic circuits and optical communication. However, the emitted light tends to be omnidirectional, which limits applications that require accurate transmission between sender and receiver. Curto et al. (p. 930; see the Perspective by Giessen and Lippitz) have designed an optical antenna, a shrunk-down version of the Yagi-Uda design used in microwave and radio communication, and show that coupling the quantum dot to the antenna provides control over the direction of the emitted light. An antenna designed for optical wavelengths is used to control the direction of the light emitted from a quantum dot. Nanoscale quantum emitters are key elements in quantum optics and sensing. However, efficient optical excitation and detection of such emitters involves large solid angles because their interaction with freely propagating light is omnidirectional. Here, we present unidirectional emission of a single emitter by coupling to a nanofabricated Yagi-Uda antenna. A quantum dot is placed in the near field of the antenna so that it drives the resonant feed element of the antenna. The resulting quantum-dot luminescence is strongly polarized and highly directed into a narrow forward angular cone. The directionality of the quantum dot can be controlled by tuning the antenna dimensions. Our results show the potential of optical antennas to communicate energy to, from, and between nano-emitters.

Polarization-sensitive broadband photodetector using a black phosphorus vertical p–n junction

The ability to detect light over a broad spectral range is central for practical optoelectronic applications, and has been successfully demonstrated with photodetectors of two-dimensional layered crystals such as graphene and MoS2. However, polarization sensitivity within such a photodetector remains elusive. Here we demonstrate a linear-dichroic broadband photodetector with layered black phosphorus transistors, using the strong intrinsic linear dichroism arising from the in-plane optical anisotropy with respect to the atom-buckled direction, which is polarization sensitive over a broad bandwidth from 400 nm to 3750 nm. Especially, a perpendicular build-in electric field induced by gating in black phosphorus transistors can spatially separate the photo-generated electrons and holes in the channel, effectively reducing their recombination rate, and thus enhancing the efficiency and performance for linear dichroism photodetection. This provides new functionality using anisotropic layered black phosphorus, thereby enabling novel optical and optoelectronic device applications.The ability to detect light over a broad spectral range is central to practical optoelectronic applications and has been successfully demonstrated with photodetectors of two-dimensional layered crystals such as graphene and MoS2. However, polarization sensitivity within such a photodetector remains elusive. Here, we demonstrate a broadband photodetector using a layered black phosphorus transistor that is polarization-sensitive over a bandwidth from ∼400 nm to 3,750 nm. The polarization sensitivity is due to the strong intrinsic linear dichroism, which arises from the in-plane optical anisotropy of this material. In this transistor geometry, a perpendicular built-in electric field induced by gating can spatially separate the photogenerated electrons and holes in the channel, effectively reducing their recombination rate and thus enhancing the performance for linear dichroism photodetection. The use of anisotropic layered black phosphorus in polarization-sensitive photodetection might provide new functionalities in novel optical and optoelectronic device applications.

Multipolar Interference for Directed Light Emission

By directing light, optical antennas can enhance light-matter interaction and improve the efficiency of nanophotonic devices. Here we exploit the interference among the electric dipole, quadrupole, and magnetic dipole moments of a split-ring resonator to experimentally realize a compact directional optical antenna. This single-element antenna design robustly directs emission even when covered with nanometric emitters at random positions, outperforming previously demonstrated nanoantennas with a bandwidth of 200 nm and a directivity of 10.1 dB from a subwavelength structure. The advantages of this approach bring directional optical antennas closer to practical applications.

Multipolar radiation of quantum emitters with nanowire optical antennas

Multipolar transitions other than electric dipoles are generally too weak to be observed at optical frequencies in single quantum emitters. For example, fluorescent molecules and quantum dots have dimensions much smaller than the wavelength of light and therefore emit predominantly as electric dipoles. Here we demonstrate controlled emission of a quantum dot into multipolar radiation through selective coupling to a linear nanowire antenna. The antenna resonance tailors the interaction of the quantum dot with light, effectively creating a hybrid nanoscale source beyond the simple Hertz dipole. Our findings establish a basis for the controlled driving of fundamental modes in nanoantennas and metamaterials, for the understanding of the coupling of quantum emitters to nanophotonic devices such as waveguides and nanolasers, and for the development of innovative quantum nano-optics components with properties not found in nature.

Strong antenna-enhanced fluorescence of a single light-harvesting complex shows photon antibunching

The nature of the highly efficient energy transfer in photosynthetic light-harvesting complexes is a subject of intense research. Unfortunately, the low fluorescence efficiency and limited photostability hampers the study of individual light-harvesting complexes at ambient conditions. Here we demonstrate an over 500-fold fluorescence enhancement of light-harvesting complex 2 (LH2) at the single-molecule level by coupling to a gold nanoantenna. The resonant antenna produces an excitation enhancement of circa 100 times and a fluorescence lifetime shortening to ~\n20 ps. The radiative rate enhancement results in a 5.5-fold-improved fluorescence quantum efficiency. Exploiting the unique brightness, we have recorded the first photon antibunching of a single light-harvesting complex under ambient conditions, showing that the 27 bacteriochlorophylls coordinated by LH2 act as a non-classical single-photon emitter. The presented bright antenna-enhanced LH2 emission is a highly promising system to study energy transfer and the role of quantum coherence at the level of single complexes.

Transparent Metallic Fractal Electrodes for Semiconductor Devices

Nanostructured metallic films have the potential to replace metal oxide films as transparent electrodes in optoelectronic devices. An ideal transparent electrode should possess a high, broadband, and polarization-independent transmittance. Conventional metallic gratings and grids with wavelength-scale periodicities, however, do not have all of these qualities. Furthermore, the transmission properties of a nanostructured electrode need to be assessed in the actual dielectric environment provided by a device, where a high-index semiconductor layer can reflect a substantial fraction of the incident light. Here we propose nanostructured aluminum electrodes with space-filling fractal geometries as alternatives to gratings and grids and experimentally demonstrate their superior optoelectronic performance through integration with Si photodetectors. As shown by polarization and spectrally resolved photocurrent measurements, devices with fractal electrodes exhibit both a broadband transmission and a flat polarization response that outperforms both square grids and linear gratings. Finally, we show the benefits of adding a thin silicon nitride film to the nanostructured electrodes to further reduce reflection.

Near-field focusing with optical phase antennas

We investigate the near-field focusing properties of three-dimensional phase antennas consisting of concentric rings designed to have source and image spots separated by several microns from the lens. Tight focal spots are obtained for silicon or gold rings patterned in a silica matrix. We analyze in detail the dependence of the performance of these lenses on geometrical parameters such as the number of rings, the ring thickness, and the focal distance. Subwavelength focal spots are found to form at distances of tens of wavelengths from the lens, thus suggesting applications to remote sensing and penlight microscopy and lithography.

Near-Field Optical Phase Antennas for Long-Range Plasmon Coupling

Plasmon-mediated long-range coupling of optical excitations is shown to be attainable using near-field phase antennas involving nanoparticles situated at focal spots. The antennas rely on metal-surface features that are geometrically arranged to produce constructive interference of plasmons emanating from a source spot over a designated image position. Large image-field intensities and focal spots as narrow as one-third of the wavelength are obtained for source-image separations of tens of micrometers. The ability to strongly couple distant focal spots through phase accumulation produced by engineered plasmon scatterers opens up a vast range of possibilities in contactless plasmon sensing, optical interconnects, and microscopy.

Silicon Mie resonators for highly directional light emission from monolayer MoS 2

Controlling light emission from quantum emitters has important applications, ranging from solid-state lighting and displays to nanoscale single-photon sources. Optical antennas have emerged as promising tools to achieve such control right at the location of the emitter, without the need for bulky, external optics. Semiconductor nanoantennas are particularly practical for this purpose because simple geometries such as wires and spheres support multiple, degenerate optical resonances. Here, we start by modifying Mie scattering theory developed for plane wave illumination to describe scattering of dipole emission. We then use this theory and experiments to demonstrate several pathways to achieve control over the directionality, polarization state and spectral emission that rely on a coherent coupling of an emitting dipole to optical resonances of a silicon nanowire. A forward-to-backward ratio of 20 was demonstrated for the electric dipole emission at 680 nm from a monolayer MoS2 by optically coupling it to a silicon nanowire.Based on a modified Mie scattering theory, several pathways to achieve control over the directionality, polarization state and spectral emission that rely on a coherent coupling of an emitting dipole in monolayer MoS2 to optical resonances of a silicon nanowire are reported.

Nanoantenna enhanced emission of light-harvesting complex 2: the role of resonance, polarization, and radiative and non-radiative rates

Nanoantennae show potential for photosynthesis research for two reasons; first by spatially confining light for experiments which require high spatial resolution, and second by enhancing the photon emission of single light-harvesting complexes. For effective use of nanoantennae a detailed understanding of the interaction between the nanoantenna and the light-harvesting complex is required. Here we report how the excitation and emission of multiple purple bacterial LH2s (light-harvesting complex 2) are controlled by single gold nanorod antennae. LH2 complexes were chemically attached to such antennae, and the antenna length was systematically varied to tune the resonance with respect to the LH2 absorption and emission. There are three main findings. (i) The polarization of the LH2 emission is fully controlled by the resonant nanoantenna. (ii) The largest fluorescence enhancement, of 23 times, is reached for excitation with light at λ = 850 nm, polarized along the long antenna-axis of the resonant antenna. The excitation enhancement is found to be 6 times, while the emission efficiency is increased 3.6 times. (iii) The fluorescence lifetime of LH2 depends strongly on the antenna length, with shortest lifetimes of ∼40 ps for the resonant antenna. The lifetime shortening arises from an 11 times resonant enhancement of the radiative rate, together with a 2-3 times increase of the non-radiative rate, compared to the off-resonant antenna. The observed length dependence of radiative and non-radiative rate enhancement is in good agreement with simulations. Overall this work gives a complete picture of how the excitation and emission of multi-pigment light-harvesting complexes are influenced by a dipole nanoantenna.