Electrochemical synthesis of straight, separable, cylindrical nanowires for use as cantilevered mechanical resonators is the main focus of this dissertation. These types of nanowires are significant for many applications, but particularly so for chip-based sensor arrays made for ultrasensitive mass detection. Directed-assembly of nanowire-based devices has enabled the development of large-area fabrication of sensor devices with new functions such as cancer detection at early stage. Chemically stable noble metals gold and rhodium are interesting materials for making nanowire resonators. Gold makes a well-known, stable and strong bond with the thiol group, which enables a range of surface functionalization chemistries. Rhodium nanowires have desirable mechanical properties for resonant mass sensing as they can retain high quality factor (Q-factor) from high vacuum to near atmospheric pressures. As a versatile and inexpensive tool, electrodeposition provides the most suitable synthesis path for gold and rhodium resonator-grade nanowires in nanoporous templates. In this work, the structural characteristics of nanoporous membranes anodized aluminium oxide and track-etched polycarbonate was explored for use as electrodeposition template. New chemistries for making gold and rhodium nanowires are introduced. Although gold cyanide-based solutions work well for the electrochemical synthesis of separable nanowires, the toxicity of cyanide solutions makes non-cyanide alternatives desirable. However, electrochemical synthesis of gold nanowires in templates from non-cyanide solutions suffers from serious drawbacks. These include growth-arresting pellet formation, poor length control and defects such as inclusions. In this dissertation, the first electrochemical synthesis of straight, cylindrical, separable gold nanowires from a sulfite-based solution is presented. This work demonstrates a scheme that suppresses electroless particle growth in the weakly-complexed gold in solution by proper use of additives. The electrochemical nucleation and growth of rhodium nanowires from a sulphate-based solution is also discussed. The effect of pH on the length uniformity as well as the effect of EDTA and polyethylenimine as additives on the development of the wire nanostructure was studied. This study has shown that the control over hydrogen co-reduction on the electrode surface and its bubble transport rate allowed for tailoring the nanostructure of the grown nanowires. The control over electrochemical nucleation and growth of noble metal films for nanowire clamping has also been investigated in this work for making reliable defect-free clamps for nanoresonator measurements. Silver was introduced as a reliable replacement for gold for nanowire clamping. Resonance measurements of rhodium nanowires clamped with silver, confirmed a reliable and repeatable clamp with very small scatter in the plot of resonance frequency variation with appropriate geometric terms. In addition, we found that the elastic modulus of a set of rhodium nanowires synthesized and measured in this work, was 14% larger than in previous studies. / Graduate / 0794 / 0548 / mascotella@gmail.com

Mit Fe-Pd-Legierungen nahe der Zusammensetzung Fe70Pd30 kann man aufgrund des thermischen oder magnetischen Formgedächtniseffekts große Dehnungen erzeugen. Daher sind sie für Mikro- und Nanoaktoren sowie Sensoren von großem wissenschaftlichen und technologischen Interesse. Im Vergleich zu Massivmaterial und dünnen Schichten erwartet man für eindimensionale Geometrien wie Nanodrähte deutlich höhere Arbeitsfrequenzen und Dehnungen. Zur Herstellung von Nanodrähten eignet sich die elektrochemische Abscheidung in selbstordnende nanoporöse Membranen als effizienteste Methode gegenüber lithographischen oder physikalischen Methoden. Um den Formgedächtniseffekt auch in Fe-Pd-Nanodrähten mit ca. 30 at.% Pd zu nutzen, werden in dieser Arbeit entsprechende Herstellungsbedingungen wie Elektrolytsystem, Abscheideparameter und Nachbehandlung herausgearbeitet. Die Zusammenhänge zwischen Abscheidebedingungen und Morphologie, lokaler Mikrostruktur, Struktur sowie magnetischen Eigenschaften werden untersucht und bewertet. Es wird gezeigt, dass Fe-Pd-Nanodrähte trotz der Kombination aus edlem und unedlem Metall elektrochemisch hergestellt werden können. Ein komplexierter Fe-Pd-Elektrolyt in Kombination mit optimierten alternierenden Abscheidepotentialen führt reproduzierbar zu durchgehenden, nahezu defektfreien Nanodrähten nahe der Zusammensetzung Fe70Pd30. Mit einer nachträglichen Wärmebehandlung erreicht man eine vollständige Umwandlung der Fe-Pd-Legierung von der kubisch raumzentrierten zur kubisch flächenzentrierten Struktur. Die erfolgreiche Herstellung dieser Nanodrähte stellt eine Schlüsselposition auf dem Weg zu formgedächtnisbasierten Nanoaktoren dar. In dieser Arbeit konnten wichtige Ansatzpunkte zur Strukturkontrolle während der elektrochemischen Abscheidung und somit zur Aktivierung des Formgedächtniseffekts identifiziert werden. / Fe-Pd alloys at about 30 at.% Pd allow obtaining high length changes or strains in the percent range due to thermal or magnetic shape memory effect. They are especially promising candidates for smart and intelligent materials in micro- and nanoactuators as well as sensors. In comparison to bulk materials and thin films the utilization of nanowires promises higher actuation frequencies and strains, which further heighten the scientific and technological interest. Electrodeposition within self-organized nanoporous templates is a very time efficient method to prepare even large arrays of Fe-Pd nanowires of different length and diameter compared to lithographic or physical methods. The aim of this work is to exhibit the preparation conditions such as electrolyte system, deposition parameter and post treatment for shape memory active Fe-Pd nanowires at about 30 at.% Pd. Correlations between morphology, local microstructure, structure and magnetic properties are investigated and evaluated. Fe-Pd nanowires are successfully prepared by electrodeposition despite the combination of noble Pd and less noble Fe metals. The usage of an electrolyte with complexed Fe and Pd ions and an optimized alternating potential deposition regime leads to continuous and almost defect free nanowires close to the composition Fe70Pd30. The complete transition from the bcc to fcc structure of the Fe-Pd alloy is achieved by an additional heat treatment. However, the successful preparation of these nanowires represents a key element towards nanoactuators based on shape memory alloys. Fundamental knowledge about electrochemical preparation of Fe-Pd nanowires is gained. Important starting points towards structure control during deposition and activation of the shape memory effect are identified.

Microelectronics integration continuously follows the trend of miniaturisation for which the technologies enabling fine pitch interconnection are in high demand. The recent advancement in the assembly of Hybrid Pixel Detectors, a high resolution detecting and imaging device, is an example of where novel materials and processes can be applied for ultra-fine pitch interconnections. For this application, indium is often used for the fine pitch bump bonding process due to its unique properties that make it especially suitable, in particular in a cryogenic environment where some types of detector have to serve. Indium bumps are typically fabricated through vacuum evaporation at the wafer level; however, this thesis investigates an alternative low cost manufacturing process at the wafer scale for the deposition of indium micro-bumps through electroplating. The work has placed its emphasis on the requirements of future technologies which will enable a low temperature (<150oC), high density interconnection (> 40,000 IOs/cm2) with a high throughput and high production yield. This research is a systematic investigation of the wafer-scale indium bumping process through electrodeposition using indium sulphamate solution. An intensive experimental study of micro-bump formation has been carried out to elaborate the effects of two of the main electroplating factors that can significantly influence the quality of bumps in the course of electrodeposition, namely the current distribution and mass transport. To adjust the current density distribution, various waveforms of current input, including direct current (DC), unipolar pulse current and bipolar pulse reverse current, were employed in the experiments. To assist mass transportation prior to or during electroplating, acoustic agitation including ultrasonic agitation at 30 kHz frequency as well as megasonic agitation at 1 MHz, were utilised. The electrochemical properties of the indium sulphamate solution were first investigated using non-patterned plain substrates prior to indium bumping trials. This provided understanding of the microstructural characteristics of indium deposits produced by electroplating and, through cathodic polarisation measurements, the highest current density suitable for electrodeposition was achieved as approximately 30 mA/cm2 when electroplating was carried out at room temperature and with no agitation applied. The typical surface morphology of DC electroplated indium contained a granular structure with a surface feature size as large as 10 µm. Pulse and pulse reverse electroplating significantly altered the surface morphology of the deposits and the surface became much smoother. By introducing acoustic agitation, the current density range suitable for electrodeposition could be significantly expanded due to the greater mass transfer, which led to a higher speed of deposition with high current efficiency. Wafer-scale indium bumping (15 µm to 25 µm diameter) at a minimum pitch size of 25 µm was successfully developed through electroplating trials with 3 inch test wafers and subsequently applied onto the standard 4 inch wafers. The results demonstrate the capability of electroplating to generate high quality indium bumps with ultrafine pitch at a high consistency and yield. To maximise the yield, pre-wetting of the ultrafine pitch photoresist patterns by both ultrasonic or megasonic agitation is essential leading to a bumping yield up to 99.9% on the wafer scale. The bump profiles and their uniformity at both the wafer and pattern scale were measured and the effects of electrodeposition regimes on the bump formation evaluated. The bump uniformity and microstructure at the feature scale were also investigated by cross-sectioning the electroplated bumps from different locations on the wafers. The growth mechanism of indium bumps were proposed on the basis of experimental observation. It was found that the use of a conductive current thief ring can homogenise the directional bump uniformity when the electrical contact is made asymmetrically, and improve the overall uniformity when the electrical contact is made symmetrically around the periphery of the wafer. Both unipolar pulse electroplating and bipolar pulse reverse electroplating improved the uniformity of the bump height at the wafer scale and pattern scale, and the feature scale uniformity could be significantly improved by pulse reverse electroplating. The best uniformity of 13.6% for a 4 inch wafer was achieved by using pulse reverse electroplating. The effect of ultrasonic agitation on the process was examined, but found to cause damage to the photoresist patterns if used for extended periods and therefore not suitable for use throughout indium bumping. Megasonic agitation enabled high speed bumping without sacrifice of current efficiency and with little damage to the photoresist patterns. However, megasonic agitation tended to degrade some aspects of wafer scale uniformity and should therefore be properly coupled with other electroplating parameters to assist the electroplating process.

Carbon foams are among the existing electrode designs proposed for use in 3D Li-ion microbatteries. For such electrodes to find applications in practical microbatteries, however, their void sizes, specific surface areas and pore volumes need be optimized. This thesis concerns the synthesis of highly porous carbon foams and their multifunctional applications in 3D microbatteries. The carbon foams are derived from polymers that are obtained by polymerizing high internal phase water-in-oil emulsions (HIPEs). In general, the carbonization of the sulfonated polymers yielded hierarchically porous structures with void sizes ranging from 2 to 35 µm and a BET specific surface area as high as 630 m2 g-1. Thermogravimetric and spectroscopic evidence indicated that the sulfonic acid groups, introduced during sulfonation, transformed above 250 oC to thioether (-C-S-) crosslinks which were responsible for the thermal stability and charring tendency of the polymer precursors. Depending on the preparation of the HIPEs, the specific surface areas and void-size distributions were observed to vary considerably. In addition, the pyrolysis temperature could also affect the microstructures, the degree of graphitization, and the surface chemistry of the carbon foams. Various potential applications were explored for the bespoke carbon foams. First, their use as freestanding active materials in 3D microbatteries was studied. The carbon foams obtained at 700 to 1500 oC suffered from significant irreversible capacity loss during the initial discharge. In an effort to alleviate this drawback, the pyrolysis temperature was raised to 2200 oC. The resulting carbon foams were observed to deliver high, stable areal capacities over several cycles. Secondly, the possibility of using these structures as 3D current collectors for various active materials was investigated in-depth. As a proof-of-concept demonstration, positive active materials like polyaniline and LiFePO4 were deposited on the 3D architectures by means of electrodeposition and sol-gel approach, respectively. In both cases, the composite electrodes exhibited reasonably high cyclability and rate performance at different current densities. The syntheses of niobium and molybdenum oxides and their potential application as electrodes in microbatteries were also studied. In such applications, the carbon foams served dual purposes as 3D scaffolds and as reducing reactants in the carbothermal reduction process. Finally, a facile method of coating carbon substrates with oxide nanosheets was developed. The approach involved the exfoliation of crystalline VO2 to prepare dispersions of hydrated V2O5, which were subsequently cast onto CNT paper to form oxide films of different thicknesses.

This thesis describes the development of a fast rate method for the deposition of high quality CdS and CdTe thin films. The technique uses Pulsed DC Magnetron Sputtering (PDCMS). Surprisingly, the technique produces highly stable process conditions. CREST is the first laboratory worldwide to show that pulsed DC power may be used to deposit CdS and CdTe thin films. This is a very promising process technology with potential for eventual industrial deployment. The major advantage is that the process produces high deposition rates suitable for use in solar module manufacturing. These rates are over an order of magnitude faster than those obtained by RF sputtering. In common with other applications it has also been found that the energetics of the pulsed DC process produce excellent thin film properties and the power supply configuration avoids the need for complex matching circuits. Conventional deposition methodologies for CdS, Chemical Bath Deposition (CBD) and CdTe thin films, Electrodeposition (ED), have been chosen as baselines to compare film properties with Pulsed DC Magnetron Sputtering (PDCMS). One of the issues encountered with the deposition of CdS thin films (window layers) was the presence of pinholes. A Plasma cleaning process of FTO-coated glass prior to the deposition of the CdS/CdTe solar cell has been developed. It strongly modifies and activates the TCO surface, and improves the density and compactness of the deposited CdS thin film. This, in turn, improves the optical and morphological properties of the deposited CdS thin films, resulting in a higher refractive index. The pinhole removal and the increased density allows the use of a much thinner CdS layer, and this reduces absorption of blue spectrum photons and thereby increases the photocurrent and the efficiency of the thin film CdTe cell. Replacing the conventional magnetic stirrer with an ultrasonic probe in the chemical bath (sonoCBD) was found to result in CdS films with higher optical density, higher refractive index, pinhole and void-free, more compact and uniform along the surface and through the thickness of the deposited material. PDCMS at 150 kHz, 500 W, 2.5 μs, 2 s, results in a highly stable process with no plasma arcing. It allows close control of film thickness using time only. The CdS films exhibited a high level of texture in the <001> direction. The grain size was typically ~50 nm. Pinholes and voids could be avoided by reducing the working gas pressure using gas flows ii below 20 sccm. The deposition rate was measured to be 1.33 nm/s on a rotating substrate holder. The equivalent deposition rate for a static substrate is 8.66 nm/s, which is high and much faster than can be achieved using a chemical bath deposition or RF magnetron sputtering. The transmission of CdS can be improved by engineering the band gap of the CdS layer. It has been shown that by adding oxygen to the working gas pressure in an RF sputtering deposition process it is possible to deposit an oxygenated CdS (CdS:O) layer with an improved band gap. In this thesis, oxygenated CdS films for CdTe TF-PV applications have been successfully deposited by using pulsed DC magnetron sputtering. The process is highly stable using a pulse frequency of 150 kHz and a 2.5 μs pulse reverse time. No plasma arcing was detected. A range of CdS:O films were deposited by using O2 flows from 1 sccm to 10 sccm during the deposition process. The deposition rates achieved using pulsed DC magnetron sputtering with only 500 W of power to the magnetron target were in the range ~1.49 nm/s ~2.44 nm/s, depending on the oxygen flow rate used. The properties of CdS thin films deposited by pulsed DC magnetron sputtering and chemical bath deposition have been studied and compared. The pulsed DC magnetron sputtering process produced CdS thin films with the preferred hexagonal <001> oriented crystalline structure with a columnar grain growth, while sonoCBD deposited films were polycrystalline with a cubic structure and small grainy crystallites throughout the thickness of the films. Examination of the PDCMS deposited CdS films confirmed the increased grain size, increased density, and higher crystallinity compared to the sonoCBD CdS films. The deposition rate for CdS obtained using pulsed DC magnetron sputtering was 2.86 nm/s using only 500 W power on a six inch circular target compared to the much slower (0.027 nm/s) for the sonoChemical bath deposited layers. CdTe thin films were grown on CdS films prepared by sonoCBD and Pulsed DC magnetron sputtering. The results showed that the deposition technique used for the CdS layer affected the growth and properties of the CdTe film and also determined the deposition rate of CdTe, being 3 times faster on the sputtered CdS. PDCMS CdTe layers were deposited at ambient temperature, 500 W, 2.9 μs, 10 s, 150 kHz, with a thickness of approximately 2 μm on CdS/TEC10 coated glass. The layers appear iii uniform and smooth with a grain size less than 100 nm, highly compact with the morphology dominated by columnar grain growth. Stress analysis was performed on the CdTe layers deposited at room temperature using different gas flows. Magnetron sputtered thin films deposited under low gas pressure are often subject to compressive stress due to the high mobility of the atoms during the deposition process. A possible way to reduce the stress in the film is the post-deposition annealing treatment. As the lattice parameter increased; the stress in the film is relieved. Also, a changing the deposition substrate temperature had an effect on the microstructure of CdTe thin films. Increasing the deposition temperature increased the grain size, up to ~600 nm. CdTe thin films with low stress have been deposited on CdS/TEC10 coated glass by setting the deposition substrate temperature at ~200°C and using high argon flows ~ 70 sccm Ar. Finally, broadband multilayer ARCs using alternate high and low refractive index dielectric thin films have been developed to improve the light transmission into solar cell devices by reducing the reflection of the glass in the extended wavelength range utilised by thin-film CdTe devices. A four-layer multilayer stack has been designed and tested, which operates across the wavelength range used by thin-film CdTe PV devices (400 850 nm). Optical modelling predicts that the MAR coating reduces the WAR (400-850 nm) from the glass surface from 4.22% down to 1.22%. The application of the MAR coating on a thin-film CdTe solar cell increased the efficiency from 10.55% to 10.93% or by 0.38% in absolute terms. This is a useful 3.6% relative increase in efficiency. The increased light transmission leads to improvement of the short-circuit current density produced by the cell by 0.65 mA/cm2. The MAR sputtering process developed in this work is capable of scaling to an industrial level.

Nanostructured porous materials generally, and nanoporous noble metals specifically, have received considerable attention due to their superior chemical and physical properties over nanoparticles and bulk counterparts. This dissertation work aims to develop well-established strategies for the preparation of multifunctional nanostructured porous materials based on the combination of inorganic-chemistry, organic-chemistry and electrochemistry. The preparation strategies involved one or more of the following processes: sol-gel synthesis, co-electrodeposition, metal ions reduction, electropolymerization and dealloying or chemical etching. The study did not stop at the preparation limits but extended to investigate the reaction mechanism behind the formation of these multifunctional nanoporous structures in order to determine the different factors controlling the nanoporous structures formation. First, gold-silica nanocomposites were prepared and used as a building blocks for the fabrication of high surface area gold coral electrodes. Well-controlled surface area enhancement, film thickness and morphology were achieved. An enhancement in the electrode’s surface area up to 57 times relative to the geometric area was achieved. A critical sol-gel monomer concentration was also noted at which the deposited silica around the gold coral was able to stabilize the gold corals and below which the deposited coral structures are not stable. Second, free-standing and transferable strata-like 3D porous polypyrrole nanostructures were obtained from chemical etching of the electrodeposited polypyrrole-silica nanocomposite films. A new reaction mechanism was developed and a new structural directing factor has been discovered for the first time. Finally, silver-rich platinum alloys were prepared and dealloyed in acidic medium to produce 3D bicontinuous nanoporous platinum nanorods and films with a nanoporous gold-like structure. The 3D-BC-NP-Pt displayed high surface area, typical electrochemical sensing properties in an aqueous medium, and exceptional electrochemical sensing capability in a complex biofouling environment containing fibrinogen. The 3D-BC-NP-Pt displayed high catalytic activity toward the methanol electro-oxidation that is 30 times higher that of planar platinum and high volumetric capacitance of 400 F/cm3. These findings will pave the way toward the development of high performance and reliable electrodes for catalysis, sensing, high power outputs fuel cells, battery-like supercapacitors and miniaturized device applications.

Dans ce travail nous étudions l’élaboration, la caractérisation et les applications de différents matériaux poreux. L’étude est organisée en trois parties majeures: la synthèse de zéolithes micro/mesoporeux et leur application potentielle dans l’industrie pétrochimique, l’étude théorique de mécanismes réactionnels sur des zeolites microporeux, et le design de métaux mesoporeux avec une chiralité intrinsèque de leur surface interne. Ces matériaux poreux montrent des propriétés excellentes, notamment pour des applications potentielles en catalyse et comme interfaces chirales. / In the present work, the elaboration, characterisation and applications of differentporous materials have been studied. Porous materials are divided into three categoriesdepending on the porous cavity size, namely microporous materials (pore diameter < 2nm), mesoporous materials (2 nm < pore diameter < 50 nm) and macroporous materials(pore diameter > 50 nm). The thesis work is organized in three major parts: the synthesisof hierarchical micro/mesoporous zeolites and their potential application for thepetrochemical industry, the theoretical study of reaction mechanisms on microporouszeolite and the design of mesoporous metals with intrinsic chirality at their inner surface.The hierarchical micro/mesoporous zeolite, composed of microporous andmesoporous features, has been prepared using carbon-silica (C/SiO2) composites derivedfrom a pyrolysis of hydrocarbon gas on silica gel. Our findings demonstrate that not onlythe presence of a high surface area and porosity, but also an improved efficiency of thesematerials for many petrochemical processes such as n-butene isomerization, nhexadecanecatalytic cracking and hydrocracking. The novel synthetic method is expectedto be generalized for other types of zeolites, and is considered to be a promising methodfor creating hierarchical micro/mesoporous zeolites for potential catalytic applications,especially in the petrochemical industry.In addition to the study of practical catalytic aspects, a theoretical approach hasbeen used to investigate potential reaction mechanisms such as the selective isomerizationof 1-butene into isobutene. More specifically, the monomolecular skeletal isomerizationof 1-butene into isobutene on H-FER zeolite was theoretically studied by using theONIOM approach. This process was found to involve the transformation of adsorbed 1-butene through 2-butoxide, isobutoxide, and tert-butyl cation intermediates. The ratedeterminingstep is the conversion of isobutoxide into isobutene, in which the reactionhas to proceed through the primary isobutyl cation transition state. The shape selectivitydue to the “nano-confinement” effect of the zeolite framework strongly affects theadsorption, the stability of alkoxide species and carbenium ion, as well as the skeletalisomerization mechanism of 1-butene.Moreover, the microporous and mesoporous zeolite, the generation of chiralmesoporous metal and its enantioselective recognition properties have been studied.Molecular imprinting (MI) is a major approach for generating materials withenantioselective properties. In this work, a chiral imprinted mesoporous platinum hasbeen obtained by the electrochemical reduction of platinum salts in the simultaneouspresence of a lyotropic liquid crystal phase and chiral template molecules. The resultingmaterials exhibit not only a dramatic increase in active surface area due to theirmesoporosity, but also a significant discrimination between two enantiomers of a chiralprobe, confirmed by both electrochemical and enantioselective adsorption experiments.Most importantly the porous platinum retains its chiral character even after removal of thechiral template molecule. Our findings could lead to the development of new materials,which are of potential interest for applications in areas such as chiral synthesis, sensors,separation, purification and drug development.

Abstract Template assisted deposition was used to produce various nanomaterials including simple nanowires, nanorods, multi-segmented metal nanowires, core-shell nanowires, alloy and polymer wires and tubes. Anodized aluminum oxide (AAO) membranes were used as templates for the growth of the various structures using an electrochemical deposition method and also by wetting the porous templates. In the electrochemical deposition method, the pore size of the templates affects the rate of synthesis and the structures of the nanomaterials while in the wetting method, the viscosity and reaction time in the polymer solution influence the structures of the nanomaterials. A conventional two-step anodization procedure was used to synthesize thick AAO templates with porous hexagonal channels at a constant applied voltage and temperature. A maximum thickness of over 180 µm oxide layer could be fabricated using mild anodization at 60 V and 80 V. Compared to conventional mild anodization, these conditions facilitated faster growth of oxide layers with regular pore arrangement. Polyethylene glycol (PEG) containing ferromagnetic nanowires were synthesized using template assisted electrochemical deposition method. During the synthesis, simultaneous deposition of polymer and metal ions resulted nanowires coated with a uniform layer of PEG without interfering with the structure and magnetic properties of the nanowires. PEG-coated Ni nanowires were embedded in polyethylene diacrylate (PEGDA) matrix after the removal of the AAO templates. Comparison of results with and without a magnetic field during embedding showed that the presence of magnetic field supported embedding of nanowire arrays in polymer. Influence of using AAO templates with several pore diameters for the synthesis of bimetallic nanowires were studied by growing Ni-Fe and Ni-Co bi-metallic nanowires. At a constant applied current by using templates with a pore diameters of 60 nm alloy formed while with a pore diameter of 130 nm core-shell nanowires formed. Polyvinylidene fluoride (PVDF) films and nanotubes were synthesized using a solution recrystallization method that favored the formation of piezoelectric β phase thin films. Variation in the concentration of polymer in the mixture solution allowed synthesis of different types of structures such as PVDF composites, nanorods and nanocrystals with tunable morphologies. Keywords: One-dimensional structures, electrodeposition, porous alumina, ferromagnetic nanostructures, magnetic core-shell nanowires, alloys, polymer composite, stimuli-active, PEGDA, azobenzene, and PVDF.

Este trabalho trata do estudo da eletrodeposição de filmes finos e nanofios magnéticos compostos de cobalto, níquel e molibdênio. Foi avaliada a influência da composição química das soluções utilizadas nas propriedades do material obtido. O uso de uma célula de Hull com eletrodo cilíndrico rotativo permitiu também que fosse estudado com mais detalhe o mecanismo de eletrodeposição da liga CoNiMo. Os filmes finos magnéticos de CoNi e CoNiMo foram eletrodepositados galvanostaticamente utilizando soluções contento citrato ou glicina como aditivo. Composição, microestrutura, morfologia e propriedades magnéticas dos depósitos foram analisados e a influência da composição das soluções e das densidades de corrente aplicadas foi avaliada. Soluções contendo citrato e/ou baixo pH não resultaram em filmes com boas propriedades. O uso de glicina e pH 7 resultou em filmes amorfos e com melhores propriedades magnéticas: magnetização de saturação de 1,2 T e coercividade de 50 Oe. Com o uso da célula de Hull rotativa foi possível avaliar como variava a composição da liga e as densidades de corrente parciais de cada um dos elementos. Notou-se que a deposição de Ni era menor quanto maior a concentração de Co+2 na solução e que o aumento na concentração de glicina favorece a deposição de Co e Mo e prejudica a deposição de Ni. Além disso, a deposição de Mo foi mais influenciada pela concentração de Co+2 do que pela de Ni+2. Tais observações podem ser analisadas com base nos mecanismos já propostos para deposição de Co, Ni e Mo. Nanofios das ligas CoNi e CoNiMo foram preparados através de eletrodeposição potenciostática utilizando membranas comerciais de alumina como molde. Glicina foi utilizada como agente complexante nos eletrólitos. Fios amorfos com diâmetro médio de 200 nm e até 50 &#181;m de comprimento foram obtidos. Em comparação com os filmes finos estudados previamente, os nanofios apresentaram maiores coercividade e cristalinidade. A coercividade medida foi de 220 Oe com o campo magnético aplicado em paralelo aos fios e de 350 Oe com o campo aplicado perpendicularmente. A presença do molibdênio não afetou as características magnéticas dos nanofios. / This work focuses on the electrodeposition of CoNi and CoNiMo thin films and nanowires. The influence of the chemical composition of several tested solutions over the properties of the material were evaluated. A rotating cylinder Hull cell allowed a more detailed study of the deposition mechanism. The thin films were galvanostatic electrodeposited from solutions containing either citrate or glycine as additives. The composition, microstructure, morphology and magnetic properties of the deposits were analyzed and related with the different bath compositions used and the applied current densities. Baths containing citrate and/or at low pH are not suitable conditions to produce magnetic films with reasonable good properties to be used in magnetic devices. Generally, use of glycine in the bath and pH 7 yielded better films. Magnetic saturation values around 1.2 T and coercivities as low as 50 Oe were obtained for films prepared using baths containing glycine. Films electrodeposited with the citrate containing baths showed higher coercivity: 125 Oe. The investigation of a wide variation of parameters the electrodeposition of the CoNiMo alloys was performed using a rotating cylinder Hull cell. Alloy composition, current efficiency and partial currents of each metal were analyzed. The nickel deposition rate decreased by increasing Co ions and glycine in the electrolyte. The latter also resulted in na augmented concentration of Ni-Gly complexed species. Molybdenum induced codeposition was verified for both excess Ni and excess Co electrolytes. The results indicate that Mo reduction was affected by the Co/Ni ratio in the electrolyte. With an excess Ni in solution, Mo wt. % increased with an increase in cobalt ion electrolyte concentration. On the other hand, with an excess of cobalt in solution, Mo wt. % was not significantly affected by nickel ion concentration. These results were analysed based on the current proposed mechanisms for Co, Ni and Mo deposition. CoNi and CoNiMo nanowires were electrodeposited using commercial alumina templates and a pH 7 glycine-ammonia electrolyte. The resulting magnetic properties and composition were compared with thin film counterparts. The nanowires had larger coercivity (220 Oe) and more crystallinity than the thin. The presence of molybdenum had no significant influence over the coercivity and remanence in the nanowires, unlike thin films.

De nouveaux électrocatalyseurs avec nanofilm de platine pour la réaction de réduction de l'oxygène avec application dans des piles à combustible à membrane échangeuse de protons ont été développés. Ces catalyseurs comprennent des films minces de platine déposés sur des réseaux de nanofibres de carbone. Des supports de nanofibres de carbone et de nanobrosse ont été préparés par électrofilage suivi de traitements thermiques pour la stabilisation et la graphitisation. Une méthode innovante d’électrodéposition pulsée à surpotentiel élevé a été développée pour le dépôt de nanofilm de platine sur des supports de nanofibres de carbone et de nanobrosse, ainsi que sur du graphite pyrolytique hautement orienté dont la planéité permet de caractériser le dépôt avec microscopie à force et électronique. Ces approches ont conduit à des électrodes en nanofibres autosupportées avec une porosité qui a été accordée à un matériau de plus en plus dense d'un côté à l'autre, où le côté présentant la plus grande surface était utilisé pour déposer du platine. Les électrodes ont été caractérisées ex situ en utilisant voltampérométrie cyclique, en démontrant une activité plus élevée pour la réaction de réduction de l'oxygène et une durabilité contre des cycles de tension plus élevée que les catalyseurs classiques au platine sur carbone. Ces électrodes ont été assemblés directement avec une membrane et une anode et caractérisés in situ dans une pile à combustible. Des films minces de platine ont également été préparés à la surface des nanofibres de nickel en utilisant le nouvelle approche de l'échange galvanique assisté par micro-ondes ; divers paramètres expérimentaux ont été étudiés pour déterminer leur effet sur l'échange et la morphologie du platine. Les fibres de nickel@platine résultantes ont présenté une électroactivité élevée pour la réaction de réduction d'oxygène et ont été caractérisées comme des électrocatalyseurs non supportés à la cathode d'un assemblage d'électrodes à membrane; des travaux supplémentaires sont nécessaires pour les stabiliser contre la perte de nickel de l’électrocatalyseur vers l’électrolyte. / Novel platinum thin film electrocatalysts for the oxygen reduction reaction of proton exchange membrane fuel cells were developed. These catalysts comprise platinum thin films deposited on carbon nanofibrous webs. Carbon nanofibres and nanobrush supports were prepared by electrospinning followed by thermal treatments for stabilisation and graphitisation. An innovative pulsed high overpotential electrodeposition method was developed to deposit platinum thin films both on carbon nanofibre and nanobrush supports, and also on highly oriented pyrolytic graphite, the planarity of which allowed detailed characterisation of the conformity, contiguity and thickness of the platinum films using atomic force and electron microscopy. These approaches led to self-standing nanofibre electrodes with porosity that was tuned to increasingly dense material from one side to the other, where the side presenting highest surface area was used to deposit platinum. The electrodes were characterised ex situ using cycling voltammetry where they demonstrated higher activity for the oxygen reduction reaction and greater durability on voltage cycling than conventional platinum on carbon catalysts. They were also assembled directly with a membrane and anode and characterised in situ in a single fuel cell. Thin platinum films were also prepared at the surface of nickel nanofibres using a novel approach to galvanic exchange assisted by microwaves, and a range of experimental parameters was investigated to determine their effect on the extent of exchange and the resulting platinum morphology. While the resulting nickel@platinum core@shell fibres demonstrated high electroactivity for the oxygen reduction reaction and were characterised as unsupported electrocatalysts at the cathode of a membrane electrode assembly, further work is required to stabilise them against nickel leaching from the catalyst to the electrolyte.