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Enrique A Dalchiele

Publications and source records attributed to Enrique A Dalchiele.

3 recordsLinked to original sources

The influence of poly(ethylene oxide) and illumination on the copper electrodeposition process onto n-Si(100).

In this study, we examined the influence of illumination and the presence of poly(ethylene oxide) (PEO) as an additive for the copper electrodeposition process onto n-Si(100). The study was carried out by means of cyclic voltammetry (CV) and the potential steps method, from which the corresponding nucleation and growth mechanism (NGM) were determined. Likewise, a morphologic analysis of the deposits obtained at different potential values by means of atomic force microscopy (AFM) was carried out. In a first stage, Mott-Schottky measurements so as to characterize the energetics of the semiconductor/electrolyte interface were made. Also, parallel capacity measurements were carried out in order to determine the surface state density of the substrate. It was found that when PEO concentration is increased, the number of these surface states decreases. The CV results indicated that the presence of PEO inhibits the photoelectrochemical reaction of oxide formation on the surface of the semiconductor. This allows a decrease in the overpotential associated with the electrodeposition process. The analysis of the j/t transients shows that the NGM corresponds to progressive three-dimensional (3D) diffusional controlled (PN3D(Diff)), which was confirmed by the AFM technique. Neither illumination nor the presence of PEO changes the mechanisms. Their influence is in that they diminish the size of the nuclei and the speed with which these are formed, which produces a more homogeneous electrodeposit.

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Polymer-dispersed liquid-crystal voltage sensor.

We present a novel electric-field and voltage sensor based on the electro-optical properties of polymer-dispersed liquid-crystals (PDLCs). In principle, the transmittance of PDLCs is a nonlinear function of the applied electrical field. To measure an AC field we superposed to it a known DC field. This allowed us to achieve linearization of the PDLC response and to measure transmittance changes independently of the light-intensity level variations. Validation experiments are presented.

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Electrochemical reversibility of vinylferrocene monolayers covalently attached on H-terminated p-Si(100).

A reversible electrochemical behavior is demonstrated on a specially prepared redox-functionalized H-Si(100) surface, obtained via an extra-mild grafting procedure from vinylferrocene. The results of a detailed XPS and electrochemical characterization of the resulting hybrid are reported and discussed to propose it as a reference system for high-quality electroactive monolayers on Si. The investigated ferrocene derivative bears a functional group suitable for a mild route to covalent anchoring on Si, which is based on a photoinduced reaction with visible light under an inert atmosphere. Electrochemical reversibility is shown by sharp symmetric voltammograms on freshly prepared p-Si electrodes. Anodic oxide growth is responsible for the progressive degradation of the electrochemical response. Still, fast electron transfer to the surface redox species is maintained during several thousands cycles.

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