P. Reichenbach

Near-field coupling of a single fluorescent molecule and a spherical gold nanoparticle

Near-field coupling of a single gold nanoparticle (GNP) to a single fluorescent molecule is investigated here for varying separation d between the two. While the emission quantum efficiency of the coupled system generally decreases for d!0, a pronounced near-field enhancement is observed under certain conditions, partly outweighing the efficiency loss at small distances. We report on optimizing these conditions by varying the excitation field direction and the three-dimensional relative configuration between the GNP and the fluorophore. Furthermore, we examine how the sphere diameter, the surrounding medium, as well as the absorption and emission wavelengths of the molecular dipole influence the fluorescence yield. Our results are of high practical relevance for all GNP-mediated application fields such as fluorescence microscopy, scattering near-field optical microscopy, bioanalytics, and medical applications.

Nonlinear optical point light sources through field enhancement at metallic nanocones

A stable nonlinear optical point light source is investigated, based on field enhancement at individual, pointed gold nanocones with sub-wavelength dimensions. Exciting these cones with near-infrared, focused radially polarized femtosecond beams allows for tip-emission at the second harmonic wavelength (second harmonic generation, SHG) in the visible range. In fact, gold nanocones with ultra-sharp tips possess interesting nonlinear optical (NLO) properties for SHG and two-photon photoluminescence (TPPL) emission, due to the enhanced electric field confinement at the tip apex combined with centrosymmetry breaking. Using two complementary optical setups for bottom or top illumination a sharp tip SHG emission is discriminated from the broad TPPL background continuum. Moreover, comparing the experiments with theoretical calculations manifests that these NLO signatures originate either from the tip apex or the base edge of the nanocones, clearly depending on the cone size, the surrounding medium, and illumination conditions. Finally, it is demonstrated that the tip-emitted signal vanishes when switching from radial to azimuthal polarization.

Multiphoton photoluminescence contrast in switched Mg:LiNbO3 and Mg:LiTaO3 single crystals

We observed a multiphoton luminescence contrast between virgin and single-switched domains in Mg-doped LiNbO3 (LNO) and LiTaO3 (LTO) single crystals with different doping levels of 0–7 mol. % and 0–8 mol. %, respectively. A luminescence contrast in the range of 3% was measured between as-grown and electrically inverted domain areas in Mg:LNO samples, while the contrast reaches values of up to 30% for the Mg:LTO case. Under annealing, an exponential decay of the domain contrast was observed. The activation energy of about 1 eV being determined for the decay allowed a comparison with reported activation energies of associated defects, clearly illustrating a strong connection between thermal contrast decay and the H+ and Li+-ion mobility. Finally, performing similar experiments on oxidized samples undoubtedly demonstrated that the origin of the reported luminescence contrast is strongly connected with lithium ions.

Multiphoton-induced luminescence contrast between antiparallel ferroelectric domains in Mg-doped LiNbO3

We report on differentiating antiparallel ferroelectric domains in congruent Mg-doped LiNbO3 (Mg:LNO) single crystals through a multiphoton photoluminescence technique. Sample illumination with femtosecond laser pulses at λ = 790 nm results in a broad multiphoton emission spectrum revealing a domain contrast of >3% between virgin and inverted domains. The contrast decreases via annealing and shows an exponential decay in the temperature range from 80 to 150 °C. Our findings give clear ground of a thermally induced structural change by surpassing a specific activation energy. Hence, the reported contrast dynamics must be closely connected to the thermal activation of charged defects, which dramatically alters the internal bias field of these defects. This explanation is also supported when using single crystal LNO of different Mg doping levels showing much lower multiphoton effects for a < 5% Mg concentration. Based on this effect of multiphoton luminescence, it becomes easy to microscopically monitor and ...

Immobilized Multifunctional Polymersomes on Solid Surfaces: Infrared Light-Induced Selective Photochemical Reactions, pH Responsive Behavior, and Probing Mechanical Properties under Liquid Phase

Fixing polymersomes onto surfaces is in high demand not only for the characterization with advanced microscopy techniques but also for designing specific compartments in microsystem devices in the scope of nanobiotechnology. For this purpose, this study reports the immobilization of multifunctional, responsive, and photo-cross-linked polymersomes on solid substrates by utilizing strong adamantane-β-cyclodextrin host-guest interactions. To reduce nonspecific binding and retain better spherical shape, the level of attractive forces acting on the immobilized polymersomes was tuned through poly(ethylene glycol) passivation as well as decreased β-cyclodextrin content on the corresponding substrates. One significant feature of this system is the pH responsivity of the polymersomes which has been demonstrated by swelling of the immobilized vesicles at acidic condition through in situ AFM measurements. Also, light responsivity has been provided by introducing nitroveratryloxycarbonyl (NVOC) protected amine molecules as photocleavable groups to the polymersome surface before immobilization. The subsequent low-energy femtosecond pulsed laser irradiation resulted in the cleavage of NVOC groups on immobilized polymersomes which in turn led to free amino groups as an additional functionality. The freed amines were further conjugated with a fluorescent dye having an activated ester that illustrates the concept of bio/chemo recognition for a potential binding of biological compounds. In addition to the responsive nature, the mechanical stability of the analyzed polymersomes was supported by computing Youngs modulus and bending modulus of the membrane through force curves obtained by atomic force microscopy measurements. Overall, polymersomes with a robust and pH-swellable membrane combined with effective light responsive behavior are promising tools to design smart and stable compartments on surfaces for the development of microsystem devices such as chemo/biosensors.