Fluorescence Enhancement in Topologically Optimized Gallium Phosphide All-Dielectric Nanoantennas.

Nanoantennas capable of large fluorescence enhancement with minimal absorption are crucial for future optical technologies from single-photon sources to biosensing. Efficient dielectric nanoantennas have been designed, however, evaluating their performance at the individual emitter level is challenging due to the complexity of combining high-resolution nanofabrication, spectroscopy and nanoscale positioning of the emitter. Here, we study the fluorescence enhancement in infinity-shaped gallium phosphide (GaP) nanoantennas based on a topologically optimized design. Using fluorescence correlation spectroscopy (FCS), we probe the nanoantennas enhancement factor and observe an average of 63-fold fluorescence brightness enhancement with a maximum of 93-fold for dye molecules in nanogaps between 20 and 50 nm. The experimentally determined fluorescence enhancement of the nanoantennas is confirmed by numerical simulations of the local density of optical states (LDOS). Furthermore, we show that beyond design optimization of dielectric nanoantennas, increased performances can be achieved via tailoring of nanoantenna fabrication.

Plasmonic Horizon in Gold Nanosponges.

An electromagnetic wave impinging on a gold nanosponge coherently excites many electromagnetic hot-spots inside the nanosponge, yielding a polarization-dependent scattering spectrum. In contrast, a hole, recombining with an electron, can locally excite plasmonic hot-spots only within a horizon given by the lifetime of localized plasmons and the speed carrying the information that a plasmon has been created. This horizon is about 57 nm, decreasing with increasing size of the nanosponge. Consequently, photoluminescence from large gold nanosponges appears unpolarized.

Anticorrelation of Photoluminescence from Gold Nanoparticle Dimers with Hot-Spot Intensity.

Bulk gold shows photoluminescence (PL) with a negligible quantum yield of ∼10-10, which can be increased by orders of magnitude in the case of gold nanoparticles. This bears huge potential to use noble metal nanoparticles as fluorescent and unbleachable stains in bioimaging or for optical data storage. Commonly, the enhancement of the PL yield is attributed to nanoparticle plasmons, specifically to the enhancements of scattering or absorption cross sections. Tuning the shape or geometry of gold nanostructures (e.g., via reducing the distance between two nanoparticles) allows for redshifting both the scattering and the PL spectra. However, while the scattering cross section increases with a plasmonic redshift, the PL yield decreases, indicating that the common simple picture of a plasmonically boosted gold luminescence needs more detailed consideration. In particular, precise experiments as well as numerical simulations are required. Hence, we systematically varied the distance between the tips of two gold bipyramids on the nanometer scale using AFM manipulation and recorded the PL and the scattering spectra for each separation. We find that the PL intensity decreases as the interparticle coupling increases. This anticorrelation is explained by a theoretical model where both the gold-intrinsic d-band hole recombination probabilities as well as the field strength inside the nanostructure are considered. The scattering cross section or the field strength in the hot-spot between the tips of the bipyramids are not relevant for the PL intensity. Besides, we not only observe PL supported by dipolar plasmon resonances, but also measure and simulate PL supported by higher order plasmonic modes.

Gold nanostars for random lasing enhancement.

We demonstrate random lasing with star-shaped gold nanoparticles ("nanostars") as scattering centers embedded in a dye-doped gain medium. It is experimentally shown that star-shaped gold nanoparticles outperform those of conventional shapes, such as spherical or prolate nanoparticles. The nanoparticles are randomly distributed within a thin film of gain medium, forming resonators which support coherent laser modes. Driven by single-pulsed excitation, the random lasers exhibit coherent lasing thresholds in the order of 0.9 mJ/cm(2) and spectrally narrow emission peaks with linewidths less than 0.2 nm. The distinguished random laser comprising nanostars is likely to take advantage of the high plasmonic field enhancements, localized at the spiky tips of the nanostars, which improves the feedback mechanism for lasing and increases the emission intensity of the random laser.

Single-Photon Emitting Arrays by Capillary Assembly of Colloidal Semiconductor CdSe/CdS/SiO2 Nanocrystals.

The controlled placement of colloidal semiconductor nanocrystals (NCs) onto planar surfaces is crucial for scalable fabrication of single-photon emitters on-chip, which are critical elements of optical quantum computing, communication, and encryption. The positioning of colloidal semiconductor NCs such as metal chalcogenides or perovskites is still challenging, as it requires a nonaggressive fabrication process to preserve the optical properties of the NCs. In this work, periodic arrays of 2500 nanoholes are patterned by electron beam lithography in a poly(methyl methacrylate) (PMMA) thin film on indium tin oxide/glass substrates. Colloidal core/shell CdSe/CdS NCs, functionalized with a SiO2 capping layer to increase their size and facilitate deposition into 100 nm holes, are trapped with a close to optimal Poisson distribution into the PMMA nanoholes via a capillary assembly method. The resulting arrays of NCs contain hundreds of single-photon emitters each. We believe this work paves the way to an affordable, fast, and practical method for the fabrication of nanodevices, such as single-photon-emitting light-emitting diodes based on colloidal semiconductor NCs.

Plasmonic Nanostars as Efficient Broadband Scatterers for Random Lasing.

Huge spectral coverage of random lasing throughout the visible up to the infrared range is achieved with star-shaped gold nanoparticles ("nanostars"). As intrinsically broadband scattering centers, the nanostars are suspended in solutions of various laser dyes, forming randomly arranged resonators which support coherent laser modes. The narrow emission line widths of 0.13 nm or below suggest that gold nanostars provide an efficient coherent feedback for random lasers over an extensive range of wavelengths, all together spanning almost a full optical octave from yellow to infrared.

Optical Plasmons of Individual Gold Nanosponges.

The search for novel plasmonic nanostructures, which can act simultaneously as optical detectors and stimulators, is crucial for many applications in the fields of biosensing, electro- and photocatalysis, electrochemistry, and biofuel generation. In most of these areas, a large surface-to-volume ratio, as well as high density of active surface sites, is desirable. We investigate sponge-like, that is, fully porous, nanoparticles, called nanosponges, where both the gold and the air phase are fully percolated in three dimensions. We correlate, on a single nanoparticle basis, their optical scattering spectra (using dark field microscopy) with their individual morphology (using electron microscopy). We find that the scattering spectra of nanosponges depend only weakly on their size and outer shape, but are greatly influenced by their unique percolation, in qualitative agreement with numerical simulations.

Random Lasing with Systematic Threshold Behavior in Films of CdSe/CdS Core/Thick-Shell Colloidal Quantum Dots.

While over the past years the syntheses of colloidal quantum dots (CQDs) with core/shell structures were continuously improved to obtain highly efficient emission, it has remained a challenge to use them as active materials in laser devices. Here, we report random lasing at room temperature in films of CdSe/CdS CQDs with different core/shell band alignments and extra thick shells. Even though the lasing process is based on random scattering, we find systematic dependencies of the laser thresholds on morphology and laser spot size. To minimize laser thresholds, optimizing the film-forming properties of the CQDs, proven by small-angle X-ray scattering, was found to be more important than the optical parameters of the CQDs, such as biexciton lifetime and binding energy or fluorescence decay time. Furthermore, the observed systematic behavior turned out to be highly reproducible after storing the samples in air for more than 1 year. These highly reproducible systematic dependencies suggest that random lasing experiments are a valuable tool for testing nanocrystal materials, providing a direct and simple feedback for further development of colloidal gain materials toward lasing in continuous wave operation.