Pyrite Photoanode/Redox Electrolyte Interface: Characterization of the Interaction of the Reducing Species with Pyrite Through Temperature Dependence Measurements

At the semiconductor pyrite photoanode/electrolyte interface, the interaction of the reducing species containing-electrolyte was investigated by temperature dependence measurements. An increase of negative entropy turnover could be related to negatively charged species interacting with the positively charged pyrite surface. Further studies, using the impedance technique in darkness and under illumination, showed that kinetic and diffusion- -like processes control this interface. In the determination of the activation energy both dc and ac techniques lead to compatible results

Développement de catalyseurs cathodiques nanométriques sélectifs à l'environnement organique pour leur utilisation dans une pile microfluidique

Les piles à combustible sans membrane polymérique comme les piles à combustible microfluidique ont des perspectives très intéressantes pour des applications énergétiques à basse puissance. L'étude menée consistait donc à poursuivre le développement de catalyseurs cathodiques nanométriques pouvant être utilisés en tant que cathode dans une pile à combustible microfluidique directe. Au cours de ce travail de thèse, une modification du comportement catalytique du platine a été réalisée grâce à un effet de support, d'alliage avec un métal de transition 3d (titane), ou bien encore par coordination de la surface de nanoparticules de platine avec un élément chalcogène (sélénium). Les effets induits par ces modifications sur les propriétés électroniques du matériau catalytique, et leurs implications sur son activité catalytique ont été étudiés au même titre que sa stabilité et sa tolérance vis-à-vis de petites molécules organiques. Les études ont été menées dans le but de présenter un nouveau paradigme des relations structure-activité, structure-stabilité et structure-tolérance gouvernant le comportement catalytique d'une surface de platine. Les expériences ont par voie de conséquence été conduites de façon à pouvoir séparer les effets catalytiques induits par le support, de ceux induits par un effet d'alliage ou bien encore par coordination des atomes de surface avec un élément chalcogène. En conclusion, ces études ont démontrés l'effet de l'interaction du métal avec le support (oxyde ou matériau carboné présentant divers degrés de graphitisation) sur l'activité et la stabilité des catalyseurs. Un autre point important, qui a été développé dans ce travail de thèse, est la modifFuel cells without polymeric membrane such as the microfluidic fuel cells (MFFC) possess very interesting perspectives for low-power energy applications. The study aimed at pursuing the development of nanometric cathodic catalysts and to study their activity, stability and tolerance in a microfluidic system. In the present thesis, the activity, stability and tolerance of Pt-based nanoparticle electrocatalysts were investigated. The effect of the support materials and the influence of surface modification by a second element including 3d transition metal (titanium) and chalcogenide (selenium) were studied. The separation and reduction of the complexity of the interaction between nanoparticles-support and nanoparticles modification by a second element enables to achieve a clear relationship of the structure-activity-stability-tolerance of the supported fuel-cell electrocatalysts. The present experimental results from the effects of the support materials and of the modification of Pt by a second element led to improve activity, stability and tolerance. The developed approach and acquired knowledge about surface property correlation can be further generalized and used in the design of advanced selective electrocatalysts. Furthermore, the synthesized electrocatalysts were used as cathode in an organic microfluidic fuel cell.POITIERS-SCD-Bib. électronique (861949901) / SudocSudocFranceF

Performance Study of Platinum Nanoparticles Supported onto MWCNT in a Formic Acid Microfluidic Fuel Cell System

The Pt/MWCNT and Pt/C catalysts were synthesized using the carbonyl chemical route. The catalysts were physically and electrochemically characterized. An enhanced stability under potential cycling is obtained with Pt/MWCNT as compared to that of Pt/C. The evaluation of the electrochemical stability in a microfluidic fuel cell system was in good agreement with the results obtained in half-cell tests. Increasing the applied current from 10 to 40 mA, the Pt/MWCNT cathode potential in the fuel cell system depolarized 67 less than Pt/C. The performance of the fuel cell with Pt/MWCNT cathode was 2 times higher compared to Pt/C, under a constant current of 40 mA for 1000 s. The results from half-cell and fuel cell measurements showed that Pt/MWCNT is a more suitable cathode for microfluidic fuel cell than Pt/C due to the properties of the carbonaceous substrate. The Pt/MWCNT cathode was subsequently used in a formic acid microfluidic fuel cell to study several system parameters including formic acid concentration, cell orientation and bubble effect

Tailoring nanostructured catalysts for electrochemical energy conversion systems

This review covers topics related to the synthesis of nanoparticles, the anodic and cathodic electrochemical reactions and low temperature electrochemical energy devices. The thermodynamic aspects of nucleation and growth of nanoparticles are discussed. Different methods of chemical synthesis such as w/o microemulsion, Bönnemann, polyol and carbonyl are presented. How the electrochemical reactions take place on the surface of the catalytic nanoparticles and the importance of the substrate is put in evidence. The use of nanomaterials in low temperature energy devices such as H2/O2 polymer electrolyte or proton exchange membrane fuel cell (PEMFC) and micro-direct methanol fuel cell (μDMFC), as well as recent progress and durability, is discussed. Special attention is given to the novel laminar flow fuel cell (LFFC). This review starts with the genesis of catalytic nanoparticles, continues with the surface electrochemical reactions that occur on them, and finally it discusses their application in electrochemical energy devices such as low temperature fuel cells or Li-air batteries

Electrochemical Surface Science: Basics and Applications

Electrochemical surface science (EC-SS) is the natural advancement of traditional surface science (where gas–vacuum/solid interfaces are studied) to liquid (solution)/electrified solid interfaces. Such a merging between two different disciplines—i.e., surface science (SS) and electrochemistry—officially advanced ca. three decades ago. The main characteristic of EC-SS versus electrochemistry is the reductionist approach undertaken, inherited from SS and aiming to understand the microscopic processes occurring at electrodes on the atomic level. A few of the exemplary keystone tools of EC-SS include EC-scanning probe microscopies, operando and in situ spectroscopies and electron microscopies, and differential EC mass spectrometry (DEMS). EC-SS indirectly (and often unconsciously) receives a great boost from the requirement for rational design of energy conversion and storage devices for the next generation of energetic landscapes. As a matter of fact, the number of material science groups deeply involved in such a challenging field has tremendously expanded and, within such a panorama, EC and SS investigations are intimately combined in a huge number of papers. The aim of this Special Issue is to offer an open access forum where researchers in the field of electrochemistry, surface science, and materials science could outline the great advances that can be reached by exploiting EC-SS approaches. Papers addressing both the basic science and more applied issues in the field of EC-SS and energy conversion and storage materials have been published in this Special Issue

Carbon-supported cubic CoSe2 catalysts for oxygen reduction reaction in alkaline medium

International audienceA Carbon-supported CoSe2 nanocatalyst has been developed as an alternative non-precious metal electrocatalyst for oxygen reduction reaction (ORR) in alkaline medium. The catalyst was prepared via a surfactant-free route and its electrocatalytic activity for the ORR has been investigated in detail in 0.1 M KOH electrolyte at 25 degrees C using rotating disk electrode (RDE) and rotating ring-disk electrode (RRDE) techniques. The prepared catalyst showed promising catalytic activity towards ORR in a four-electron transfer pathway and higher tolerance to methanol compared to commercial Pt/C catalyst in 0.1 M KOH. To some extent, the increase of CoSe2 loading on the electrode favors a faster reduction of H2O2 intermediate to H2O. (C) 2012 Elsevier Ltd. All rights reserved

Application of Metal Organic Framework (MOF) in the electrocatalytic process

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The Effect of Support on Advanced Pt-based Cathodes towards the Oxygen Reduction Reaction. State of the Art

International audienceThis work summarizes the advanced materials developed by various research groups for improving the stability of platinum (Pt), and Pt-based catalysts center toward the oxygen reduction reaction (ORR) in acid medium. The ORR stability enhancement of Pt catalytic center can be classified according to the different nature of the supporting materials, namely, carbon-, oxide-based-, and oxide-carbon composites. The enhancement and stability of a catalytic center can be related to either its electronic modification induced by a strong interaction with the support, another metal (alloy), or to geometric effects. In addition, other parameters come into play, the size, the morphology of the catalytic center, the temperature, the dispersion, and mass loading, along with the measuring methods. This mini-review mainly focusses on the stability improvement, depending on the substrate nature. This latter can be further modified via functionalization or by the chemical interaction nature between the substrate and catalyst