Synthesis and characterization of anisotropic micro- and nanoparticles, either in suspension or localized on a surface, are current areas of intense scientific interest because of their shape-tunable material properties with potential applications in catalysis, microelectronics, data storage and pharmaceutics. Electrochemical deposition represents a facile and versatile route to fabricate anisotropic particles since it offers a high degree of freedom in monitoring and manipulating particle growth processes. The first part of my dissertation presents an additive-mediated electrochemical approach to fabricate anisotropic copper micro- and nanoparticles. This work explores the possibility of using anisotropic copper particles as novel non-noble metal alternatives to expensive anode electrocatalysts (platinum and palladium) used in direct methanol fuel cells (DMFCs). Characterization using SEM, EDS, XRD and TEM confirms the anisotropic morphology and crystal structure of synthesized copper particles. A possible mechanism for anisotropic crystal growth is proposed based on preferential adsorption of additive ions onto selective crystal faces. Methanol oxidation is chosen as model experiment to test the electrocatalytic property of copper particles towards DMFC applications. Characterization using cyclic voltammetry demonstrates shape dependent enhancement in electrocatalytic activity of anisotropic copper particles for methanol oxidation. Chronoamperometry and thermal stability measurements indicate good catalyst stability and durability under steady-state conditions. The second part of my dissertation presents a novel electrochemical fabrication route to generate randomly rough surfaces over large areas. Surface roughness directly affects a material's performance at its functional interface. This work shows that by simple tuning of electrochemical deposition potential for a metal onto an electrode, island nucleation density can be systematically varied. Changes in nucleation density results in generation of thin films with different nanoscale surface roughness. Characterization using AFM illustrates the change in surface topography with applied potential. The fabricated roughness is successfully replicated onto other moldable soft materials (polystyrene and polyurethane) through an embossing and curing step. Roughness gradients were also generated by introducing a controlled mechanical retraction step to the process. Gradient surfaces serve as an effective probing tool for investigating a range of surface parameters in quick time using single experiment, enabling a cost-effective and high-throughput screening method. / acase@tulane.edu

Le réchauffement climatique est dû principalement à l'émission anthropique du dioxyde de carbone (CO2) dans l'atmosphère. Une réduction électrocatalytique et sélective de cette molécule a été proposée au cours de ce projet comme une solution prometteuse pour synthétiser des produits à valeur ajoutée. Une telle réaction requiert l'utilisation de matériaux efficaces et bas coût. Pour ce faire, les travaux de cette thèse ont porté sur la préparation de catalyseurs à base de cuivre dispersés sur différents substrats carbonés tels que le Vulcan XC-72R, les carbones mésoporeux CMK-3 et FDU-15, et des tanins à base d'IS2M pour réduire le CO2 en milieu aqueux. Les matériaux d'électrode ont été préparés à l'aide de la méthode polyol assistée par micro-ondes. Leurs caractérisations physiques et l'analyse élémentaire confirment des compositions atomiques et des taux de charge métallique proches de celles théoriquement envisagées. L'acide formique et le monoxyde de carbone sont les deux produits carbonés issus de la réduction du CO2 (2 bar) réalisée par chronoampérométrie en milieu NaHCO3. La détection et l'identification des produits de réaction ont été effectuées par des méthodes chromatographiques (µ-GC et HPLC), spectrométrique (DEMS) et spectroscopique (RMN). Une sélectivité de la réaction vis-à-vis de HCOOH (62 %) a été obtenue sur une cathode de Cu50Pd50/C. Cette conversion sélective du CO2 en HCOOH s'explique par une conjugaison d'effets électroniques et géométriques dans la structure de surface du catalyseur bimétallique et aussi celui de la texture du substrat carboné. / The anthropogenic emissions of carbon dioxide (CO2) are the major cause of global warming. The selective CO2 reduction reaction (CO2RR) of has been proposed as a promising, convenient and efficient method for sustainable energy conversion systems. The reduction of CO2 to energetically valuable products requires the use of an appropriate electrode material. This study focuses on the preparation of Cu-based electrocatalysts supported on different types of carbon materials such as Vulcan XC-72R, mesoporous carbon CMK-3, mesoporous carbon FDU-15 and tannin based mesoporous carbon IS2M for the CO2RR under mild conditions. Besides, Vulcan XC-72R carbon supported bimetallic copper/palladium alloy materials were prepared for increasing the Faradaic yield. These copper-based catalysts were electrochemically characterized and preparative electrolyses set at constant potential were carried out in order to investigate the reduction products distribution and Faradaic yields as a function of the applied potential and catalyst loading. Chemicals such as HCOOH, CO and H2 issued from the CO2RR, were determined with in-situ and ex-situ complementary (electro)analytical and spectroscopic techniques. The significant difference in the product distribution is probably due to the ensemble (geometry and ligand) effects in the bimetallic CuPd materials, and textural structure of the supporting substrates. Selective CO2 to-HCOOH conversion has been successfully undertaken on Cu50Pd50/C with 62 % Faradaic efficiency.