Geometry-induced enhancement factor improvement in covered-gold-nanorod-dimer antennas

Illuminated gapped-gold-nanorod dimers hold surface plasmon polaritons (SPPs) that can be engineered, by an appropriate choice of geometrical parameters, to enhance the electromagnetic field at the gap, allowing applications in molecular detection via surface-enhanced Raman spectroscopy (SERS). Envisioning hybrid devices in which the SERS spectroscopy of molecules in the gap is complemented by electrical measurements, it arises the question of designing efficient geometries to contact the nanorods without decreasing the enhancement factor (EF) of the nanoantenna, i.e., the figure of merit for SERS spectroscopy. Within this framework we theoretically study the feasibility to fabricate designs based on covering with gold the far-from-the-gap areas of the dimer. We show that by tuning the geometrical parameters of the designs these systems can reach enhancement factors larger than the best achieved in the uncovered dimer: this supremacy survives even in the presence of dimer asymmetries and vacancies at the interfaces between the nanorods and the covering layers. Our results show that geometrical modifications away from the gap can improve the optical response at the gap, thus enabling the use of these devices both for hybrid and optical applications.Comment: 10 pages, 8 figure

Effect of the excitation setup in the improved enhancement factor of covered-gold-nanorod-dimer antennas

Devices possessing the ability to sense both electrically and optically molecular targets are of fundamental and technological interest. Towards this end, it has been shown that covering the ends of gapped gold-nanorod-dimer nanoantennas can improve the enhancement factor (EF) that quantifies the nanoantenna efficiency for surface-enhancement Raman spectroscopy (SERS) for an incident wave coming from the top of the sample. Here, as the covering breaks the top-bottom symmetry, we investigate the behaviour of the EF for excitation coming from the bottom of the sample. This is relevant in presence of a reflecting substrate or due to the placement of the device in a cavity field. We also study the case of a superposition of waves coming from both directions in the limit cases in which a node or an antinode of the total incident field lies at the center of the gold nanorods. In all these situations we find that the EF of the covered device can continue to be higher than for the uncovered case when the geometrical parameters are tuned to the peak values of the calculated enhancement factor

SPR Biosensing MUA/Poly-L-lysine Platform for the Detection of 2,4-Dinitrophenol as Small Molecule Model System

Surface Plasmon Resonance assays are being developed as alternative biodetection methods for a great number of pesticides and toxins. These substances typically have low molecular weight, making it necessary to perform competitive inhibition immunoassays. In most of the cases, the strategy is to immobilize a protein derivative of the analyte, which usually involves the appearance of nonspecific protein binding which limits the detection range of the assay. In this work we present results of a poly-L-lysine (Au-MUA-PLL) based sensor platform for quantitative determination of 2,4-dinitrophenol as model system for small molecular weight substances detection. The prepared sensor chip was characterized by means of Atomic Force Microscopy, Surface Plasmon Resonance, and Surface Enhanced Raman Spectroscopy. Experiments verified the absence of nonspecific protein adsorption to Au-MUA-PLL surfaces and the improvement of the competitive inhibition assays performance in comparison with single and mixed thiol self-assembled monolayers. The possibility of directly immobilizing 2,4-dinitrophenol to the poly-L-lysine containing platforms leads to an improvement in the detection of the soluble analyte by the competitive inhibition assay avoiding undesirable nonspecific protein adsorption. Therefore, Au-MUA-PLL surfaces constitute a suitable alternative for quantitative detection of small molecules when nonspecific adsorption cannot be avoided.Instituto de Investigaciones Fisicoquímicas Teóricas y AplicadasInstituto de Estudios Inmunológicos y FisiopatológicosFacultad de Ciencias Exacta

La búsqueda de la identidad en el período 1975-1983

A partir del análisis de resoluciones y expedientes judiciales conservados en el Archivo General de los Tribunales de Córdoba, mediante el relevamiento y sistematización de los procesos de guardas y adopciones tramitados entre 1975 y 1983 en los Juzgados de Menores y Juzgados Civiles, el proyecto se propone: identificar casos potenciales de apropiación de hijos de personas víctimas del Terrorismo de Estado, y elaborar una base de datos que contribuya a dar respuesta a las consultas sobre identidad presentadas ante el Poder Judicial de Córdoba. Es un trabajo cuya mirada se centra en la escena judicial de la época del “Proceso de Reorganización Nacional” con el propósito de colaborar en la promoción de los derechos humanos y la restitución de derechos vulnerados.Fil: Bonzano, María de los Ángeles. Universidad Católica de Córdoba. Facultad de Derecho y Ciencias Sociales; Argentin

La búsqueda de la identidad en el período 1975-1983

A partir del análisis de resoluciones y expedientes judiciales conservados en el Archivo General de los Tribunales de Córdoba, mediante el relevamiento y sistematización de los procesos de guardas y adopciones tramitados entre 1975 y 1983 en los Juzgados de Menores y Juzgados Civiles, el proyecto se propone: identificar casos potenciales de apropiación de hijos de personas víctimas del Terrorismo de Estado, y elaborar una base de datos que contribuya a dar respuesta a las consultas sobre identidad presentadas ante el Poder Judicial de Córdoba. Es un trabajo cuya mirada se centra en la escena judicial de la época del “Proceso de Reorganización Nacional” con el propósito de colaborar en la promoción de los derechos humanos y la restitución de derechos vulnerados.Fil: Bonzano, María de los Ángeles. Universidad Católica de Córdoba. Facultad de Derecho y Ciencias Sociales; Argentin

SPR Biosensing MUA/Poly-L-lysine Platform for the Detection of 2,4-Dinitrophenol as Small Molecule Model System

Surface Plasmon Resonance assays are being developed as alternative biodetection methods for a great number of pesticides and toxins. These substances typically have low molecular weight, making it necessary to perform competitive inhibition immunoassays. In most of the cases, the strategy is to immobilize a protein derivative of the analyte, which usually involves the appearance of nonspecific protein binding which limits the detection range of the assay. In this work we present results of a poly-L-lysine (Au-MUA-PLL) based sensor platform for quantitative determination of 2,4-dinitrophenol as model system for small molecular weight substances detection. The prepared sensor chip was characterized by means of Atomic Force Microscopy, Surface Plasmon Resonance, and Surface Enhanced Raman Spectroscopy. Experiments verified the absence of nonspecific protein adsorption to Au-MUA-PLL surfaces and the improvement of the competitive inhibition assays performance in comparison with single and mixed thiol self-assembled monolayers. The possibility of directly immobilizing 2,4-dinitrophenol to the poly-L-lysine containing platforms leads to an improvement in the detection of the soluble analyte by the competitive inhibition assay avoiding undesirable nonspecific protein adsorption. Therefore, Au-MUA-PLL surfaces constitute a suitable alternative for quantitative detection of small molecules when nonspecific adsorption cannot be avoided.Instituto de Investigaciones Fisicoquímicas Teóricas y AplicadasInstituto de Estudios Inmunológicos y FisiopatológicosFacultad de Ciencias Exacta