Thesis (M.S.)--Mississippi State University. Department of Chemistry. / Title from title screen. Includes bibliographical references.

Thesis (Ph. D.)--University of Texas at Austin, 2000. / Vita. Includes bibliographical references. Available also in a digital version from Dissertation Abstracts.

Metallophthalocyanines and metal nanoparticles were successfully synthesized and applied for the electrooxidation of amitrole, nitrite and hydrazine individually or when employed together. The synthesized materials were characterized using the following techniques: predominantly scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), electrochemistry and scanning electrochemical microscopy (SECM). Different electrode modification methods were used to modify the glassy carbon substrates. The methods include adsorption, electrodeposition, electropolymerization and click chemistry. Modifying the glassy carbon substrate with MPc (electropolymerization) followed by metal nanoparticles (electrodeposition) or vice versa, made a hybrid modified surface that had efficient electron transfer. This was confirmed by electrochemical impedance studies with voltammetry measurements having lower detection potentials for the analytes. This work also describes for the first time the micropatterning of the glassy carbon substrate using the SECM tip. The substrate was electrografted with 4-azidobenzenediazonium salt and then the click reaction was performed using ethynylferrocene facilitated by Cu⁺ produced at the SECM tip. The SECM imaging was then used to show the clicked spot.

A presente tese versa sobre resultados obtidos na aplicação da microscopia eletroquímica de varredura no estudo de sistemas micelares e no estudo de bicamadas lipídicas. Os estudos envolvendo sistemas micelares foram realizados utilizando a SECM no modo substrato-gerador/microeletrodo-coletor. Neste modo de operação, um microeletrodo de platina foi posicionado próximo a um substrato de platina e utilizado para monitorar espécies eletrogeradas nesse substrato. Conhecendo o tempo necessário para a espécie eletrogerada difundir do substrato até o microeletrodo, foi possível aplicar a equação de Einstein-Smoluchowski para determinar o coeficiente de difusão da espécie eletroativa e de micelas de surfactantes. Como as micelas não são eletroativas, o ferroceno eletrogerado no substrato e incorporado nas micelas foi utilizado como sonda para a estimativa do tempo de difusão. Os resultados obtidos para o surfactante brometo de tetradecil trimetil amônio (C14TABr) corroboram dados reportados na literatura, demonstrando a utilidade da metodologia proposta no estudo de sistema micelares. Também foram realizados experimentos envolvendo micelas do surfactante cloreto de 1-alquil-3-metilimidazólio, CxMelmCl (x = 10, 12, 14, 16) e com os resultados obtidos foi possível evidenciar o efeito da cadeia carbônica no coeficiente de difusão das espécies. Os experimentos envolvendo a permeação de substâncias através de bicamadas lipídicas foram realizados em duas etapas. Os primeiros ensaios foram realizados utilizando modelo de membrana semipermeável (papel celofane) com o intuito de verificar a aplicabilidade da SECM no monitoramento de espécies eletroativas que permeiam através da membrana. Na segunda etapa, apresentou-se metodologia para a obtenção de microfuros em folhas de poliestireno utilizados para a formação das bicamadas lipídicas, assim como detalhes sobre a construção da célula de medidas utilizadas nos experimentos de permeação. Foram realizados experimentos envolvendo o uso de bicamadas lipídicas planas obtidas pelo método de Miller preparadas com lecitina de soja. Esses experimentos foram realizados com o intuito de avaliar a estabilidade e para verificar a permeabilidade de algumas substâncias nas bicamadas formadas. Os experimentos de permeação foram realizados posicionando um microeletrodo próximo à membrana, com posterior detecção amperométrica da espécie eletroativa que atravessa a membrana. / This thesis shows results on the use of scanning electrochemical microscopy in the study of micellar systems and lipid bilayers. Studies involving micellar systems were performed by using SECM in the substrate-generator/tip-collector mode. In this operation mode a platinum microelectrode was positioned close to a platinum substrate and used to monitor electrogenerated species on this surface. Taking into account the time for the electrogenerated species to diffuse from the substrate to the microelectrode, the diffusion coefficient of the electroactive species and of the micelles can be calculated by applying the Einstein-Smoluchowski equation. As micelles are not electroactive, ferrocene electrogenerated on the substrate and incorporated into the micelles was used as a probe to estimate the diffusion time. The results obtained for tetradecyl trimethyl ammonium bromide (C14TABr) corroborate those reported in the literature, demonstrating the applicability of the proposed methodology in the study of micellar systems. Experiments with micelles obtained from 1-alkyl-3-methylimidazolium, CxMelmCl (x = 10, 12, 14, 16) chloride surfactants were also performed and results showed the effect of the carbon chain in the diffusion coefficient. Experiments involving the permeation of chemical species through lipid bilayers were carried out in two steps. A membrane model (cellophane) was preliminary used in order to investigate the possibility of using SECM as a tool for monitoring the permeation of electroactive species through the membrane. Then, a methodology for obtaining microholes in polystyrene sheets used to form lipid bilayers was presented, as well as details about the design of an electrochemical cell used in the permeation experiments. Experiments involving the use of planar lipid bilayers obtained by the method of Miller prepared using soybean lecithin were performed. These experiments were carried out in order to evaluate the stability and to check the permeation of some substances through the prepared bilayers. Permeation experiments were performed by placing the microelectrode close to the membrane with subsequent amperometric detection of any electroactive species that cross the membrane

Ce manuscrit décrit les travaux menés pour le développement et l'utilisation du microscope électrochimique (SECM) pour l'étude des surfaces fonctionnelles. Cette microscopie à sonde locale, utilisant les propriétés des ultramicroélectrodes (UMEs), permet l'analyse de la réactivité chimique à la surface d'un échantillon. Le but de ces travaux est alors l'analyse de surfaces fonctionnalisées par une couche organique. Dans un premier temps, nous avons développé la méthodologie du SECM par l'utilisation de sonde redox spécifique. D'abord, cela nous a permis de déterminer la distance entre l'électrode-sonde et la surface grâce à un médiateur redox irréversible comme les polyaromatiques. Ensuite, nous avons pu observer des propriétés physico-chimiques d'une surface, notamment afin de différencier les différents modes de transport électronique au travers une couche organique, grâce à l'utilisation des catéchols ou des dendrimères redox. Nous avons également commencé le développement d'un nouveau mode d'utilisation du SECM : le SECM transitoire. Dans un deuxième temps, nous avons utilisé le SECM afin d'analyser trois surfaces fonctionnalisées. La première surface est un substrat d'or fonctionnalisé par des calixarènes. La deuxième est une surface de verre sur laquelle il a été déposée des nanoparticules photosensibles, appelées « quantum rods ». Et la dernière est un substrat de silicium modifié par un récepteur anthracène. Finalement, la dernière étude qui a été menée concerne l'écriture et la lecture d'une monocouche organique grâce à la sonde du SECM. Ces modifications localisées de la couche organique sont alors de la taille de l'UME, soit de l'ordre du micromètre. Dans notre cas nous avons choisi la modification de monocouche organique auto-assemblée (SAM) sur un substrat d'or grâce à la réaction de couplage de Huisgen. En plus, de l'amélioration de nos conditions de fonctionnalisation, nous avons pu mettre en évidence un phénomène de propagation catalytique en surface grâce à un complexe spécial de cuivre (II) contenant une fonction éthynyle. / This manuscript describes the work done for the development and use of electrochemical microscope (SECM) for the investigations of functional surfaces. This local probe microscopy, using the properties of ultramicroelectrodes (UMEs), permits the analysis of chemical reactivity on the sample’s surface. The aim of this work is then analyzing surfaces functionalized with an organic layer. Initially, we have developed the SECM methodology by using specific redox probes. First, it allowed us to determine the absolute distance between the electrode and the surface, thanks to an irreversible redox mediator such as polyaromatic. Then, we could observe the physicochemical surface properties, in particular to differentiate the electronic transfer modes through an organic layer, by using catechols or redox dendrimers. We have also started the development of a new mode of SECM: transient SECM. Secondly, we used the SECM to analyze three functionalized surfaces. The first surface is a gold substrate functionalized by calixarenes. The second is a glass side on which it was deposed photosensitive nanoparticles, called "quantum rods" and the last sample is a substrate of silicon modified by anthracene receptors. Finally, the last study concerns the writing and reading on an organic monolayer with the SECM probe. These localized changes of the organic layer are about the size of the UME, of the order of a micrometer. In our case, we chose the modification of self-assembled organic monolayer (SAM) on a gold substrate by the Huisgen coupling reaction. In addition to the improvement of our conditions of functionalization, we were able to demonstrate a phenomenon of surface catalytic propagation due to a special complex of copper (II) containing ethynyl functions.

No description available.

Scanning electrochemical microscopy (SECM) is used to deposit gold nanoparticles on a glassy carbon electrode (GCE). Deposition conditions, including the tip-substrate distance, current density, substrate potential, and addition of Ag ions in the electrolyte are changed to study the effects on gold spot size and particle morphology. Atomic force microscopy (AFM) is used to analyze the gold nanoparticles. The size and shape of the nanoparticle can be controlled by different SECM experimental conditions. OMSOL Multiphysics software is used to simulate the results of SECM deposition. By comparing the simulation results and experimental results, the deposition process can be understood better. Heterogeneous irreversible reaction rate constant of the reaction happened on GCE can be estimated.

The tip generation/substrate collection mode (TG/SC) of scanning electrochemical microscopy (SECM) was used to study the ORR reactivity on Pt catalysts in sulfuric acid solution. The SECM reactivity image and the photographic image of different single crystalline regions of the etched Pt electrode correlated well. The electron backscatter diffraction (EBSD) image of Pt confirmed the surface single crystalline orientation. The image resolution is improved by employing smaller tip-substrate distance. The kinetics of the ORR on Pt surface was also studied at -15 - 30 C by means of the rotating disk voltammetry techniques. The calculated Tafel slopes for 0.1 m and 0.9 m HClO4 changed with decreasing temperature, indicating lower kinetics at low temperature. Peroxide is produced at potentials below 0 V vs SCE.

The focus of this dissertation research involves surface charge manipulation of functionalized monolayers. Application of potential to acid or base terminated organic films immobilized on electrodes results in the ionization of the terminal groups. The ionization of these groups using applied potential provides conditions favorable the control of polyelectrolyte deposition to the monolayer surface. Research is presented that asserts that the interfacial pH of acid or base terminated monolayers responds to applied potential as a result of the accumulation of phosphate counterions to the monolayer-solution interface. Results obtained from applied potential modulation of surface charge endeavors strongly suggest that manipulation of terminal group ionization with applied potential “turns on“ or “turns off“ the charge of the monolayer. Switching on the surface charge of functionalized monolayers using applied potential yields conditions that make it possible for the promotion or inhibition of electrostatic attachment of polyelectrolyte to the monolayer surface. Electrostatic interactions between immobilized polyelectrolytes and redox probes result in changes in electron transfer that can be monitored with electrochemical impedance measurements. Impedance measurements provide a qualitative assessment of the degree of potential-driven polyelectrolyte self assembly. The electrostatic interactions between the redox probe in solution and the terminal region of monolayers directly affects the extent of charge-transfer between the electrode and the redox probe in solution. For this reason, impedance measurements are able to provide an indication of whether or not potential drives to electrostatic deposition to the terminal region of a functionalized monolayer. Unlike impedance measurements, quartz crystal microbalance measurements provide quantitative mass assessments that confirm polyelectrolyte deposition of inhibition under the direction of applied potential. Application of appropriate potentials is shown to induce variations in the electrostatic interactions between redox probes in solution and terminal groups of monolayers. Variations in the electrostatic interactions between the modified electrode and the redox probe modulate electron transfer that produces varying current. Since scanning electrochemical microscopy (SECM) relies on modulation of feedback current underneath a ten-micrometer platinum tip, SECM provides a means for monitoring of potential-driven surface charge modulation. Experiments presented in this dissertation will show that in addition to monitoring the effect of applied potential on the charge of ionizable surface groups, SECM can also be used to selectively deposit a polyelectrolyte to the surface of a carboxylic acid terminated monolayer. The SECM tip was rastered over the surface of a functionalized monolayer in the form of a simple pattern while the electrode was immersed in a dilute polyelectrolyte solution. As the SECM tip was moved and potential stepped more positive than the PZC, ionization was confined ionization to one spot encouraging localized ionic self assembly. / Ph. D.

Scanning Electrochemical Microscopy (SECM) is most commonly used to spatially resolve reaction rates, image surface topography and surface reactivity. In this research, SECM is applied to various chemical systems in order to resolve local reaction chemistry and to produce patterns with dimensions of tens of microns in n-alkanethiol passivated gold substrates. Upon completing construction of the instrumentation, SECM was applied to capillary electrophoresis to accurately and reproducibly place the electrode directly above a very small capillary opening. Feedback SECM was then used to image and pattern surfaces, effectively distinguishing between insulating and conductive domains. Finally, the size of desorbed features patterned on a passivated gold substrate were studied as a function of both applied potential and ionic strength. Electrochemical detection in capillary electrophoresis requires decoupling the voltage applied to the working electrode from the separation voltage applied across the capillary. End-capillary electrochemical detection achieves this by placing the electrode just outside the ground end of the separation capillary. Obtaining adequate signal-to-noise in this arrangement requires using small inner diameter capillaries. Decreasing the inner diameter of the separation capillary, however, increases the difficulty of aligning the microelectrode with the open end of the capillary. Using SECM, the position of the capillary opening is determined while electroactive material is continuously emerging from the end of the capillary. The SECM instrument is then used to place the electrode at the position of maximum current for subsequent separations. Subsequent measurements found that the best signal-to-noise is obtained when the detection electrode is placed directly opposite the capillary opening and just outside of the capillary opening. When the electrode is further above the opening (but still opposite the capillary opening), the signal-to-noise does not dramatically decrease until the electrode is more than 30 μm above the 10 μm inner-diameter capillary. Limits of detection for 2,3-dihydroxybenzoic acid were found to be 8.2 fmol when aligned manually, and 3.8 fmol when the SECM is used to automatically align the microelectrode. SECM was then used to image a series of multi-disk electrode arrays in order to demonstrate the ability of the instrument to discriminate between conductive and insulating domains. Upon demonstrating the capacity of the SECM to image very small domains of conductor on an insulating substrate, n-alkanethiol passivated gold surfaces were patterned using site-selective desorption. A number patterns, potentially useful for enzyme deposition, were subsequently produced in the passivated gold substrate. The feature size of the desorbed domains was monitored as a function of applied potential and the ionic strength of the solution used for desorption. Results showed that applying a more negative potential or increasing the ionic strength of the solution increased the magnitude of the electric field at the surface of the passivated gold substrate and resulted in a more complete, larger desorption. Both ionic strength and applied desorption potential prove to be parameters useful for controlling the size of patterned features in site selective desorption. / Master of Science