Marco Francardi

Local tuning of photonic crystal nanocavity modes by laser-assisted oxidation

The authors demonstrate a simple method to achieve local tuning of optical modes in GaAs photonic crystal nanocavities by continuous wave laser-assisted oxidation in air atmosphere. By irradiation with a focused laser beam at power levels of a few tens of milliwatts, photonic crystal nanocavity modes shift to shorter wavelengths by up to 2.5 nm. The mode shifts can be controlled either by varying the laser power or by iterating laser-assisted oxidation steps and are well explained by finite-element-method and finite-difference time-domain simulations. This method provides a simple route to achieve fine spectral tuning of individual nanocavities for photonic devices.

Multi-scheme approach for efficient surface plasmon polariton generation in metallic conical tips on AFM-based cantilevers

We report on the possibility of realizing adiabatic surface plasmon polaritons compression on metallic conical tips built-in on AFM cantilevers by means of different approaches. The problem is faced considering the role of the source, when linear and radial polarizations are assumed, associated to different fabrication schemes. Nano-patterned devices properly combined with metallic conical tips can affect the adiabatic characteristic of the surface electric field. The results are analyzed in terms of tradeoff between fabrication difficulties and device performances. Suggestions on the best possible scheme are provided.

Enhanced spontaneous emission in a photonic-crystal light-emitting diode

We report direct evidence of enhanced spontaneous emission in a photonic-crystal (PhC) light-emitting diode. The device consists of p-i-n heterojunction embedded in a suspended membrane, comprising a layer of self-assembled quantum dots. Current is injected laterally from the periphery to the center of the PhC. A well-isolated emission peak at 1.3μm from the PhC cavity mode is observed, and the enhancement of the spontaneous emission rate is clearly evidenced by time-resolved electroluminescence measurements, showing that our diode switches off in a time shorter than the bulk radiative and nonradiative lifetimes.

Tuning of photonic crystal cavities by controlled removal of locally infiltrated water

We present a spectral tuning mechanism of photonic crystal microcavities based on microfluidics. The microinfiltration with water of one or few cavity holes and its subsequent controlled evaporation allow us to tune the cavity resonances in a spectral range larger than 20 nm, with subnanometer accuracy, and we also observe that the addition of water in the microcavity region improves its quality factor Q.

Controlling the charge environment of single quantum dots in a photonic-crystal cavity

We demonstrate that the presence of charges around a semiconductor quantum dot (QD) strongly affects its optical properties and produces nonresonant coupling to the modes of a microcavity. We show that, besides (multi)exciton lines, a QD generates a spectrally broad emission which efficiently couples to cavity modes. Its temporal dynamics shows that it is related to the Coulomb interaction between the QD (multi)excitons and carriers in the adjacent wetting layer. This mechanism is suppressed by the application of an electric field, making the QD closer to an ideal two-level system.

Near-field imaging of coupled photonic-crystal microcavities

We report by means of near-field microscopy on the coupling between two adjacent photonic crystal microcavities. Clear-cut experimental evidence of the spatial delocalization of coupled-cavity optical modes is obtained by imaging the electromagnetic local density of states. We also demonstrate that it is possible to design photonic structures with selective coupling between different modes having orthogonal spatial extensions

Enhanced spontaneous emission rate from single InAs quantum dots in a photonic crystal nanocavity at telecom wavelengths

The authors demonstrate coupling at 1.3μm between single InAs quantum dots (QDs) and a mode of a two dimensional photonic crystal (PhC) defect cavity with a quality factor of 15 000. By spectrally tuning the cavity mode, they induce coupling with excitonic lines. They perform a time integrated and time-resolved photoluminescence and measure an eightfold increase in the spontaneous emission rate inducing a coupling efficiency of 96%. These measurements indicate the potential of single QDs in PhC cavities as efficient single-photon emitters for fiber-based quantum information processing applications.

Electroless Deposition and Nanolithography Can Control the Formation of Materials at the Nano-Scale for Plasmonic Applications

The new revolution in materials science is being driven by our ability to manipulate matter at the molecular level to create structures with novel functions and properties. The aim of this paper is to explore new strategies to obtain plasmonic metal nanostructures through the combination of a top down method, that is electron beam lithography, and a bottom up technique, that is the chemical electroless deposition. This technique allows a tight control over the shape and size of bi- and three-dimensional metal patterns at the nano scale. The resulting nanostructures can be used as constituents of Surface Enhanced Raman Spectroscopy (SERS) substrates, where the electromagnetic field is strongly amplified. Our results indicate that, in electroless growth, high quality metal nanostructures with sizes below 50 nm may be easily obtained. These findings were explained within the framework of a diffusion limited aggregation (DLA) model, that is a simulation model that makes it possible to decipher, at an atomic level, the rules governing the evolution of the growth front; moreover, we give a description of the physical mechanisms of growth at a basic level. In the discussion, we show how these findings can be utilized to fabricate dimers of silver nanospheres where the size and shape of those spheres is controlled with extreme precision and can be used for very large area SERS substrates and nano-optics, for single molecule detection.

A facile in situ microfluidic method for creating multivalent surfaces: toward functional glycomics

An in situ method of modifying the chemistry and topology of microfluidic surfaces in order to mimic the cellular environment is described. The binding of functionalised microbeads to microfluidic channels allows the surface-to-volume ratio of the system, and thus the number of biomolecules available for reaction, to be vastly increased, thereby enhancing the sensitivity of biochemical analyses. The sensitivity and specificity of the technique were first investigated via the study of carbohydrate-protein interactions. Beads featuring hydrazide moieties were adhered to the channel surface, after which carbohydrates (galactose and mannose) were bound to the beads in situ and reacted with fluorescently labelled proteins. Results showed a six-fold increase in fluorescent signal compared to the same process performed on a glass surface without the presence of beads, thereby demonstrating the increase in valence afforded by the method. In a subsequent study, beads, modified with galactose moieties via the in situ functionalisation technique, were used to perform studies of colon tumour cells from a cell sample. Here, the carcinoma cells exhibited superior adhesion than the normal cells due to an increased expression of active galactose receptors, thereby demonstrating the success of the biofunctionalisation method for investigating cellular mechanisms.

Protein–Carbohydrate Complex Reveals Circulating Metastatic Cells in a Microfluidic Assay

Advances in carbohydrate sequencing technologies reveal the tremendous complexity of the glycome and the role that glycomics might have to bring insight into the biological functions. Carbohydrate-protein interactions, in particular, are known to be crucial to most mammalian physiological processes as mediators of cell adhesion and metastasis, signal transducers, and organizers of protein interactions. An assay is developed here to mimic the multivalency of biological complexes that selectively and sensitively detect carbohydrate-protein interactions. The binding of β-galactosides and galectin-3--a protein that is correlated to the progress of tumor and metastasis--is examined. The efficiency of the assay is related to the expression of the receptor while anchoring to the interactions strength. Comparative binding experiments reveal molecular binding preferences. This study establishes that the assay is robust to isolate metastatic cells from colon affected patients and paves the way to personalized medicine.