Cathodoluminescence hyperspectral analysis of whispering gallery modes in active semiconductor wedge resonators.

Whispering gallery mode resonators are key devices for integrated photonics. Despite their generalization in fundamental and applied science, information on spatial confinement of light in these structures is mostly retrieved from purely spectral analysis. In this work, we present a detailed spectral and spatial characterization of whispering gallery modes in active semiconductor microdisk resonators by use of hyperspectral cathodoluminescence. By comparing our experimental findings to finite element simulations, we demonstrate that the combination of spectral and spatial measurements enables unique identification of the modes and even reveals specific features of the microresonator geometry, such as a wedge profile.

Nanowires of methylammonium lead iodide (CH3NH3PbI3) prepared by low temperature solution-mediated crystallization.

We report the synthesis of Methylammonium Lead Iodide (CH(3)NH(3)PbI(3)) nanowires by a low temperature solution processed crystallization using a simple slip-coating method. The anisotropic particle shape exhibits advantages over nanoparticles in terms of charge transport under illumination. These results provide a basis for solvent-mediated tailoring of structural properties like the crystallite size and orientation in trihalide perovskite thin films, which, once implemented into a device, may ultimately result in an enhanced charge carrier extraction.

Nanoscale optical properties of metal nanoparticles probed by Second Harmonic Generation microscopy.

We report spatial and vectorial imaging of local fields' confinement properties in metal nanoparticles with branched shapes, using Second Harmonic Generation (SHG) microscopy. Taking advantage of the coherent nature of this nonlinear process, the technique provides a direct evidence of the coupling between the excitation polarization and both localization and polarization specificities of local fields at the sub-diffraction scale. These combined features, which are governed by the nanoparticles' symmetry, are not accessible using other contrasts such as linear optical techniques or two-photon luminescence.

Synthesis and spectroscopic properties of 4-amino-1,8-naphthalimide derivatives involving the carboxylic group: a new molecular probe for ZnO nanoparticles with unusual fluorescence features.

Of a series of 4-substituted 1,8-naphthalimides, fluorescent 4-(6-piperidinyl-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)benzoic acid (4) was found to be a sensitive molecular probe for ZnO nanoparticles. We investigated in detail one- and two-photon absorption properties of this fluorophore. In nonpolar solvents, the acid 4 absorbs at about 400 nm and fluoresces at 500 nm with a fluorescence lifetime of about 7 ns, similar to the ester 6 and typical of the lifetimes of other derivatives of this type. Although the anionic form of this acid is not fluorescent, partial ionization of 4 in polar solvents, such as ethanol and acetonitrile, is not only accompanied by the expected decrease in the fluorescence quantum yield, but also gives rise to bathochromic shifts of both absorption and fluorescence and dual fluorescence with lifetimes of 0.2-0.3 ns and 6 ns ascribed to the formation of anionic complexes. The interaction with the ZnO surface brings about further considerable changes in the fluorescence patterns.

Wide-field vibrational phase imaging.

We propose and implement a wide-field microscopy method to retrieve the real and imaginary part of a field emitted by coherent and resonant molecular scatterers. The technique is based on wave-front sensing and does not require the use of any reference beam. We exemplify its ability in wide-field coherent anti-Stokes Raman scattering imaging and retrieve the complex anti-Stokes field while spectrally scanning a molecular vibrational resonance. This approach gives access to the background-free Raman spectrum of the targeted molecular bond.

Efficient NIR-light emission from solid-state complexes of boron difluoride with 2'-hydroxychalcone derivatives.

This article describes a series of nine complexes of boron difluoride with 2'-hydroxychacone derivatives. These dyes were synthesized very simply and exhibited intense NIR emission in the solid state. Complexation with boron was shown to impart very strong donor-acceptor character into the excited state of these dyes, which further shifted their emission towards the NIR region (up to 855 nm for dye 5 b, which contained the strongly donating triphenylamine group). Strikingly, these optical features were obtained for crystalline solids, which are characterized by high molecular order and tight packing, two features that are conventionally believed to be detrimental to luminescence in organic crystals. Remarkably, the emission of light from the π-stacked molecules did not occur at the expense of the emission quantum yield. Indeed, in the case of pyrene-containing dye 4, for example, a fluorescence quantum yield of about 15 % with a fluorescence emission maximum at 755 nm were obtained in the solid state. Moreover, dye 3 a and acetonaphthone-based compounds 1 b, 2 b, and 3 b showed no evidence of degradation as solutions in CH(2) Cl(2) that contained EtOH. In particular, solutions of brightly fluorescent compound 3 a (brightness: ε×Φ(f) =45,000 M(-1) cm(-1)) could be stored for long periods without any detectable changes in its optical properties. All together, these new dyes possess a set of very interesting properties that make them promising solid-state NIR fluorophores for applications in materials science.

Detection of chemical interfaces in coherent anti-Stokes Raman scattering microscopy: Dk-CARS. I. Axial interfaces.

We develop a full vectorial theoretical investigation of the chemical interface detection in conventional coherent anti-Stokes Raman scattering (CARS) microscopy. In Part I, we focus on the detection of axial interfaces (i.e., parallel to the optical axis) following a recent experimental demonstration of the concept [Phys. Rev. Lett. 104, 213905 (2010)]. By revisiting the Young's double slit experiment, we show that background-free microscopy and spectroscopy is achievable through the angular analysis of the CARS far-field radiation pattern. This differential CARS in k space (Dk-CARS) technique is interesting for fast detection of interfaces between molecularly different media. It may be adapted to other coherent and resonant scattering processes.

Detection of chemical interfaces in coherent anti-Stokes Raman scattering microscopy: D-CARS. II. Arbitrary interfaces.

We address the general problem of detecting chemical interfaces arbitrarily oriented in space in coherent anti-Stokes Raman scattering (CARS) microscopy. Such a task is accomplished by using a beam reversal scheme, as recently demonstrated experimentally [J. Biomed. Opt. 16, 086006 (2011)]. We develop a full vectorial theoretical analysis of the situation and show that transverse chemical interfaces are readily highlighted without special care in the CARS signal detection. In addition, a finer analysis reveals that adequate angular analysis of the CARS far-field radiation pattern enables the detection of axial interfaces. Background-free CARS microscopy and spectroscopy are thus achievable through the combined application of excitation beam reversal and angular analysis of the CARS far-field radiation pattern. This differential CARS (D-CARS) technique is relevant for fast detection of interfaces between molecularly different media.

An upper bound to carrier multiplication efficiency in type II colloidal quantum dots.

We experimentally investigate carrier multiplication (CM) in type II CdTe/CdSe quantum dot (QD) heterostructures by the means of a simple and robust subnanosecond transient photoluminescence spectroscopy setup. Experimental conditions were set to minimize the blurring of the CM signature by extraneous effects. The extracted photon energy threshold for CM is consistent with previous studies in CdSe and CdTe QDs (around 2.65 times the type II energy band gap) and we can infer an upper bound to CM yield. This study indicates that, while CM is probably present in type II QD heterostructures below the CM threshold for each constituent separately, it exhibits only a modest yield.

Revisiting the Young's double slit experiment for background-free nonlinear Raman spectroscopy and microscopy.

In the Young's double slit experiment, the spatial shift of the interference pattern projected onto a screen is directly related to the phase difference between the fields diffracted by the two slits. We apply this property to fields emitted by nonlinear processes and thus demonstrate background-free coherent anti-Stokes Raman scattering microscopy near an axial interface between a resonant and a nonresonant medium. This method is relevant to remove the nonresonant background in other coherent resonant processes.

Strong electromagnetic confinement near dielectric microspheres to enhance single-molecule fluorescence.

Latex microspheres are used as a simple and low-cost means to achieve three axis electromagnetic confinement below the standard diffraction limit. We demonstrate their use to enhance the fluorescence fluctuation detection of single molecules. Compared to confocal microscopy with high numerical aperture, we monitor a detection volume reduction of one order of magnitude below the diffraction limit together with a 5-fold gain in the fluorescence rate per molecule. This offers new opportunities for a broad range of applications in biophotonics, plasmonics, optical data storage and ultramicroscopy.

Second harmonic generation hotspot on a centrosymmetric smooth silver surface.

Second harmonic generation (SHG) is forbidden for materials with inversion symmetry, such as bulk metals. Symmetry can be broken by morphological or dielectric discontinuities, yet SHG from a smooth continuous metallic surface is negligible. Using non-linear microscopy, we experimentally demonstrate enhanced SHG within an area of smooth silver film surrounded by nanocavities. Nanocavity-assisted SHG is locally enhanced by more than one order of magnitude compared to a neighboring silver surface area. Linear optical measurements and cathodoluminescence (CL) imaging substantiate these observations. We suggest that plasmonic modes launched from the edges of the nanocavities propagate onto the smooth silver film and annihilate, locally generating SHG. In addition, we show that these hotspots can be dynamically controlled in intensity and location by altering the polarization of the incoming field. Our results show that switchable nonlinear hotspots can be generated on smooth metallic films, with important applications in photocatalysis, single-molecule spectroscopy and non-linear surface imaging.

Direct Fabrication of 3D Metallic Networks and Their Performance.

Fabrication of macroscopic nanoporous metallic networks is challenging, because it demands fine structures at the nanoscale over a large-scale. A technique to form pure scalable networks is introduced. The networked-metals ("Netals") exhibit a strong interaction with light and indicate a large fraction of hot-electrons generation. These hot-electrons are available to derive photocatalytic processes.

Hybridization between nanocavities for a polarimetric color sorter at the sub-micron scale.

Metallic hole arrays have been recently used for color generation and filtering due to their reliability and color tunability. However, color generation is still limited to several microns. Understanding the interaction between the individual elements of the whole nanostructure may push the resolution to the sub-micron level. Herein, we study the hybridization between silver nanocavities in order to obtain active color generation at the micron scale. To do so, we use five identical triangular cavities which are separated by hundreds of nanometers from each other. By tuning either the distance between the cavities or the optical polarization state of the incoming field, the transmitted light through the cavities is actively enhanced at specific frequencies. Consequently, a rainbow of colors is observed from a sub-micron scale unit. The reason for this is that the metallic surface plays a vital role in the hybridization between the cavities and contributes to higher frequency modes. Cathodoluminescence measurements have confirmed this assumption and have revealed that these five triangular cavities act as a unified entity surrounded by the propagated surface plasmons. In such plasmonic structures, multi-color tuning can be accomplished and may open the possibility to improve color generation and high-quality pixel fabrication.

Facile route to freestanding CH3NH3PbI3 crystals using inverse solubility.

CH3NH3PbI3 was found to exhibit inverse solubility at high temperatures in γ-butyrolactone. Making use of this unusual, so far unreported phenomenon, we present a facile method for the growth of freestanding crystals of CH3NH3PbI3 from solution without addition of any capping agents or seed particles. Large, strongly faceted crystals could be grown within minutes. This finding may aid in understanding the crystallization process of CH3NH3PbI3 from solution that may lead to improved morphological control of film deposition for a range of device architectures. Our process offers a facile and rapid route to freestanding crystals for use in a broad range of characterization techniques.

Effect of Threading Dislocations on the Quality Factor of InGaN/GaN Microdisk Cavities.

In spite of the theoretical advantages associated with nitride microcavities, the quality factors of devices with embedded indium gallium nitride (InGaN) or gallium nitride (GaN) optical emitters still remain low. In this work we identify threading dislocations (TDs) as a major limitation to the fabrication of high quality factor devices in the nitrides. We report on the use of cathodoluminescence (CL) to identify individual TD positions within microdisk lasers containing either InGaN quantum wells or quantum dots. Using CL to accurately count the number, and map the position, of dislocations within several individual cavities, we have found a clear correlation between the density of defects in the high-field region of a microdisk and its corresponding quality factor (Q). We discuss possible mechanisms associated with defects, photon scattering, and absorption, which could be responsible for degraded device performance.

Transverse chemical interface detection with coherent anti-Stokes Raman scattering microscopy.

Transverse "chemical" interfaces are revealed with a conventional two beam narrowband coherent anti-Stokes Raman scattering microscopy setup in a collinear configuration. The exciting "pump" and "Stokes" beams are focused on the sample in two opposite directions. The subtraction of the two generated anti-Stokes signals gives rise to a signal that is directly proportional to the pure Raman spectrum of the resonant medium. This property is used to highlight an interface between glass and N,N-dimethylformamide (DMF) and recover the pure Raman spectrum of DMF around its 1408 cm(-1) vibrational band.

Colloidal quantum dots as probes of excitation field enhancement in photonic antennas.

Optical antennas are essential devices to interface light to nanoscale volumes and locally enhance the electromagnetic intensity. Various experimental methods can be used to quantify the antenna amplification on the emission process, yet characterizing the antenna amplification at the excitation frequency solely is a challenging task. Such experimental characterization is highly needed to fully understand and optimize the antenna response. Here, we describe a novel experimental tool to directly measure the antenna amplification on the excitation field independently of the emission process. We monitor the transient emission dynamics of colloidal quantum dots and show that the ratio of doubly to singly excited state photoluminescence decay amplitudes is an accurate tool to quantify the local excitation intensity amplification. This effect is demonstrated on optical antennas made of polystyrene microspheres and gold nanoapertures, and supported by numerical computations. The increased doubly excited state formation on nanoantennas realizes a new demonstration of enhanced light-matter interaction at the nanoscale.

Coherent anti-Stokes Raman scattering in a microcavity.

We study tight focus coherent anti-Stokes Raman scattering (CARS) emission in a microcavity where the active medium is squeezed between two independent planar mirrors. We show strong modifications in the CARS forward and backward far-field radiation patterns. For low-order cavities, we demonstrate that most of the emitted power can be concentrated into a direction perpendicular to the mirrors.