Andrea Csáki

Optical Properties of Individual Silicon Nanowires for Photonic Devices

Silicon is a high refractive index material. Consequently, silicon nanowires (SiNWs) with diameters on the order of the wavelengths of visible light show strong resonant field enhancement of the incident light, so this type of nanomaterial is a good candidate for all kinds of photonic devices. Surprisingly enough, a thorough experimental and theoretical analysis of both the polarization dependence of the absorption and the scattering behavior of individual SiNWs under defined illumination has not been presented yet. Here, the present paper will contribute by showing optical properties such as scattering and absorption of individual SiNWs experimentally in an optical microscope using bright- and dark-field illumination modes as well as in analytical Mie calculations. Experimental and calculation results are in good agreement, and both reveal a strong correlation of the optical properties of individual SiNWs to their diameters. This finding supports the notion that SiNWs can be used in photonic applications such as for photovoltaics or optical sensors.

Preparation and Optical Characterization of Core–Shell Bimetal Nanoparticles

Chemical approaches allow for the synthesis of highly defined metal heteronanostructures, such as core–shell nanospheres. Because the material in the metal nanoparticles determines the plasmon resonance-induced absorption band, control of particle composition results in control of the position of the absorption band. Metal deposition on gold or silver nanoparticles yielded core–shell particles with modified optical properties. UV–vis spectroscopy on solution-grown, as well as surface-grown, particles was conducted and provided ensemble measurements in solution. Increasing the layers of a second metal leads to a shift in the absorption band. A shell diameter comparable to the original particle diameter leads to a predominant influence by the shell material. Extent of shell growth could be controlled by reaction time or the concentration of metal salt or reducing agent. Besides optical characterization, the utilization of atomic force microscopy, scanning electron microscopy, and transmission electron microscopy yielded important information about the ultrastructure of nanoparticle complexes. Surface-grown core–shell particles were superior in terms of achievable shell thickness, because of difficulties encountered with solution-grown particles due to salt-induced aggregation.

The optical detection of individual DNA-conjugated gold nanoparticle labels after metal enhancement

The detection of DNA using nanoparticles as labels is an interesting alternative to the standard fluorescence technique. It requires simpler detection equipment, resulting in higher stability and lower costs. Besides easier detection, metal enhancement allows a higher sensitivity of detection. The signal-response curve for labelled DNA before and after silver enhancement was studied, applying both atomic force microscope (AFM) and optical (reflection/transmission) measurements. The dynamic range and the sensitivity were determined for nanoparticle labelling with and without metal enhancement. Nanoparticle concentrations down to the fM range could be detected. The ultimate limit of detection, the identification of individual labels, is demonstrated for the optical readout. Therefore, AFM images of the particles were correlated with the optical signal of individual or clustered particles. We demonstrate that the optical signal allows the identification of single particles.

Gold nanoparticles as novel label for DNA diagnostics

The growing interest in DNA diagnostics, especially in combination with the need for highly-paralleled and miniaturized hybridization assays, is today addressed by fluorescence DNA chips. Fluorescence detection is approved and highly developed, however, it has also problematic aspects, e.g., the low stability of the dyes, the influence of the physicochemical environment onto the signal intensity and the expensive set-up for detection. A novel detection scheme based on metal nanoparticles was proposed to overcome these problems and is discussed in this review.

Nanoparticle Layer Deposition for Plasmonic Tuning of Microstructured Optical Fibers

Plasmonic nanoparticles with spectral properties in the UV-to-near-IR range have a large potential for the development of innovative optical devices. Similarly, microstructured optical fibers (MOFs) represent a promising platform technology for fully integrated, next-generation plasmonic devices; therefore, the combination of MOFs and plasmonic nanoparticles would open the way for novel applications, especially in sensing applications. In this Full Paper, a cost-effective, innovative nanoparticle layer deposition (NLD) technique is demonstrated for the preparation of well-defined plasmonic layers of selected particles inside the channels of MOFs. This dynamic chemical deposition method utilizes a combination of microfluidics and self-assembled monolayer (SAM) techniques, leading to a longitudinal homogeneous particle density as long as several meters. By using particles with predefined plasmonic properties, such as the resonance wavelength, fibers with particle-adequate spectral characteristics can be prepared. The application of such fibers for refractive-index sensing yields a sensitivity of about 78 nm per refractive index unit (RIU). These novel, plasmonically tuned optical fibers with freely selected, application-tailored optical properties present extensive possibilities for applications in localized surface plasmon resonance (LSPR) sensing.

Sensoric potential of gold–silver core–shell nanoparticles

AbstractThe sensitivities of five different core–shell nanostructures were investigated towards changes in the refractive index of the surrounding medium. The shift of the localized surface plasmon resonance (LSPR) maximum served as a measure of the (respective) sensitivity. Thus, gold–silver core–shell nanoparticles (NPs) were prepared with different shell thicknesses in a two-step chemical process without the use of any (possibly disturbing) surfactants. The measurements were supported by ultramicroscopic images in order to size the resulting core–shell structures. When compared to sensitivities of nanostructures reported in the literature with those of the (roughly spherical) gold–silver core–shell NPs, the latter showed comparable (or even higher) sensitivities than gold nanorods. The experimental finding is supported by theoretical calculation of optical properties of such core–shell NP. Extinction spectra of ideal spherical and deformed core–shell NPs with various core/shell sizes were calculated, and the presence of an optimal silver shell thickness with increased sensitivity was confirmed. This effect is explained by the existence of two overlapping plasmon bands in the NP, which change their relative intensity upon change of refractive index. Results of this research show a possibility of improving LSPR sensor by adding an extra metallic layer of certain thickness. FigureFigure: Left TEM image of gold-silver core-shell nanoparticle, Right Two images of E-field distribution in the core-shell nanoparticle at different excitation wavelengths.

Molecular plasmonics: light meets molecules at the nanoscale.

Certain metal nanoparticles exhibit the effect of localized surface plasmon resonance when interacting with light, based on collective oscillations of their conduction electrons. The interaction of this effect with molecules is of great interest for a variety of research disciplines, both in optics and in the life sciences. This paper attempts to describe and structure this emerging field of molecular plasmonics, situated between the molecular world and plasmonic effects in metal nanostructures, and demonstrates the potential of these developments for a variety of applications.

Optimization of Gold Nanoparticle-Based DNA Detection for Microarrays

DNA microarrays are promising tools for fast and highly parallel DNA detection by means of fluorescence or gold nanoparticle labeling. However, substrate modification with silanes (as a prerequisite for capture DNA binding) often leads to inhomogeneous surfaces and/or nonspecific binding of the labeled DNA. We examined both different substrate cleaning and activating protocols and also different blocking strategies for optimizing the procedures, especially those for nanoparticle labeling. Contact angle measurements as well as fluorescence microscopy, atomic force microscopy (AFM), and a flatbed scanner were used to analyze the multiple-step process. Although the examined different cleaning and activating protocols resulted in considerably different contact angles, meaning different substrate wettability, silanization led to similar hydrophobic surfaces which could be revealed as smooth surfaces of about 2–4 nm roughness. The two examined silanes (3-glycidoxypropyltrimethoxysilane (GOPS) and 3-aminopropyltriethoxysilane (APTES)) differed in their DNA binding homogeneity, maximum signal intensities, and sensitivity. Nonspecific gold binding on APTES/PDC surfaces could be blocked by treatment in 3% bovine serum albumin (BSA).

Gold-silver and silver-silver nanoparticle constructs based on DNA hybridization of thiol- and amino-functionalized oligonucleotides.

Metal nanoparticle constructs of particles of different sizes and materials were prepared, using DNA as connecting element. Therefore, gold and silver nanoparticles were functionalized with complementary DNA sequences that enabled a controlled coupling. The well-established system based on thiolated DNA was thereby complemented with amino-functionalized DNA. The realization of specific DNA-DNA bonds due to hybridization was controlled by the ionic strength. The results demonstrate the potential of the combination of different particle sizes, composition as well as coupling chemistry in order to realize controlled conjugates of nanoparticles.

Biofunctionalization of zinc oxide nanowires for DNA sensory applications

We report on the biofunctionalization of zinc oxide nanowires for the attachment of DNA target molecules on the nanowire surface. With the organosilane glycidyloxypropyltrimethoxysilane acting as a bifunctional linker, amino-modified capture molecule oligonucleotides have been immobilized on the nanowire surface. The dye-marked DNA molecules were detected via fluorescence microscopy, and our results reveal a successful attachment of DNA capture molecules onto the nanowire surface. The electrical field effect induced by the negatively charged attached DNA molecules should be able to control the electrical properties of the nanowires and gives way to a ZnO nanowire-based biosensing device.