Christine Canaff

Electrochemically induced surface modifications of mesoporous spinels (Co3O4−δ, MnCo2O4−δ, NiCo2O4−δ) as the origin of the OER activity and stability in alkaline medium

Co3O4−δ, MnCo2O4−δ, NiCo2O4−δ materials were synthesized using a nanocasting process consisting in replicating a SBA-15 hard template. Catalysts powders obtained were characterized using different physico-chemical techniques (X-ray scattering, transmission electron microscopy, N2 physisorption and X-ray photoelectron spectroscopy) in order to deeply characterize their morphostructural properties. Electrochemical measurements performed with cyclic voltammetry and electrochemical impedance spectroscopy techniques have shown that these catalysts were liable to surface modifications induced by the applied electrode potential. These surface structural modifications as well as their effect on the electroactivity of the catalyst towards the OER in alkaline medium are discussed. The activated NiCo2O4−δ material showed particularly excellent catalytic ability towards the OER in 0.1 M KOH electrolyte. In this material Co(IV) is found to be the active species in the catalyst composition for the OER. It exhibits an overpotential as low as 390 mV at a current density of 10 mA cm−2. This catalytic activity is especially high since the oxide loading is only of 0.074 mg cm−2. Furthermore, this anode catalyst showed high stability during an accelerated durability test of 1500 voltammetric cycles.

Facile synthesis of highly active and durable PdM/C (M = Fe, Mn) nanocatalysts for the oxygen reduction reaction in an alkaline medium

The efficient design of highly active and durable materials towards the ultimate goal of improving kinetics of the oxygen reduction reaction (ORR), which allow enhanced performance in solid alkaline membrane fuel cells (SAMFCs), remains elusive. Seminal studies have shown that by alloying a noble metal such as palladium to a transition metal, it is possible to tune the electronic and/or bifunctional properties enabling substantial ORR performance to be achieved, thereby designing a costly catalyst. Herein, we address and discuss new findings from deeper ORR investigations at palladium-based nanostructures in an alkaline medium. We exploited and manipulated the straightforward and fast synthesis method, the so-called “Bromide Anion Exchange”, to prepare surfactant-free PdM/C (M = Fe, Mn) nanocatalysts exhibiting unprecedented activity and stability towards ORR. PdFe/C from bromide anion exchange (BAE) enables 40- and 4-fold enhancement in terms of exchange current density and kinetic current density and ca. 100 mV gains compared to the polyol microwave-assisted method. After 20 000 cycles of accelerated potential cycling test (APCT), our findings indicate that the present PdM/C bimetallics outperform, to the best of our knowledge, most of the data reported for ORR in alkaline media for Pd-based transition metals. The improved catalytic performances are assigned to the absence of any organic contaminants or protective ligands on their surface and their relatively heterogeneous character comprising nanoalloys and nanowire oxides.

High impact of the reducing agent on palladium nanomaterials: new insights from X-ray photoelectron spectroscopy and oxygen reduction reaction

Palladium has exceptional affinity with hydrogen and the evolution of the surface of its nanomaterials prepared from chemical methods over time is still unclear. Here, the reducing agent effect on Pd nanomaterials and their long-term chemical stability were scrutinized by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The subsequent impact on the catalytic properties was examined using the electrochemical oxygen reduction reaction (ORR). We have discovered that the nature of the reducing agent has noteworthy effects on the final composition of Pd nanomaterials prepared from chemical methods. The surface state of the nanomaterials prepared by using sodium borohydride as reducing agent (Pd/C–NaBH4) is radically different from those obtained from L-ascorbic acid (Pd/C–AA). In addition to pure metal, two oxides were identified: PdO and PdOx (x > 1). XRD analysis has upheld the presence of PdO only in Pd/C–NaBH4, thus underpinning the conclusion that NaBH4 has drastically changed the Pd structure. Furthermore, the reducing agent substantially affects the electrocatalytic properties. The ORR starts with enhanced kinetics (E > 1 V vs. RHE) by a 4-electron process, producing p(H2O2) < 0.5% associated with excellent durability over 5000 cycles. Both catalysts outperform all reported data for Pd electrocatalysts. The novelty of this work is combining ex/in situ XPS and XRD analyses together with ORR as a catalytic model. Overall, this work represents a clear development in our understanding of Pd affinity towards hydrogen and paves new ways for the successful synthesis of Pd-based nanomaterials free from hydrides and oxides, and having impressive catalytic activities.

Three dimensionally ordered mesoporous hydroxylated NixCo3−xO4 spinels for the oxygen evolution reaction: on the hydroxyl-induced surface restructuring effect

Surface restructuration upon potential cycling of three dimensionally ordered NixCo3−xO4 spinels for the oxygen evolution reaction (OER) in an alkaline medium is studied using structural, spectroscopic and electrochemical techniques. It was shown that the intrinsic activity of different catalysts depends on the incorporated amount of nickel and surprisingly correlates with the CoIII/CoIV peak potential. The electrochemical activity of the OER is amazingly improved upon potential cycling. It was observed that potential cycling induces an increase of active sites up to 45% on the most effective electrocatalyst. This unexpected increase in activity is very pronounced and becomes stable after 30 voltammetric cycles. Such a phenomenon is explained by the formation of a layered mixed nickel/cobalt oxyhydroxide active site whose oxidation potential is related to the nickel amount in the catalyst. The formation of this layer is promoted by the surface hydroxylation degree of non-cycled catalysts. In these catalysts, nickel modulates the electronic properties of the active site, which modifies the adsorption energies of key oxygenated intermediates. The synthesis route proposed herein allows an efficient way for obtaining high specific surface areas as well as highly hydroxylated surfaces, the latter being the key factor in the enhancement of the electrocatalytic activity of nickel cobaltites.

Impact of Nonthermal Atmospheric Plasma on the Structure of Cellulose: Access to Soluble Branched Glucans

We have investigated the effect of non-thermal atmospheric plasma (NTAP) on the structure of microcrystalline cellulose. In particular, by means of different characterization methods, we demonstrate that NTAP promotes the partial cleavage of the β-1,4 glycosidic bond of cellulose leading to the release of short-chain cellodextrins that are reassembled in situ, preferentially at the C6 position, to form branched glucans with either a glucosyl or anhydroglucosyl terminal residue. The ramification of cellulosic chain induced by NTAP yields branched glucans that are soluble in DMSO or in water, thus opening a straightforward access to processable glucans from cellulose. Importantly, the absence of solvent and catalyst considerably facilitates downstream processing as compared to (bio)catalytic processes which typically occur in diluted conditions.

Characterization Methods for Components and Materials

This chapter gives a general view of various spectroscopic and electron microscopic techniques that are common and increasingly used for the physiochemical characterization of fuel cell materials. The measuring principle of the X-ray photoelectron spectroscopy (XPS), the scanning electron microscopy (SEM), the transmission electron microscopy (TEM), the atomic force microscopy (AFM), the infrared (IR) spectroscopy, and the Raman spectroscopy method are simplified and described by a selected example for each characterization method. The gained insights from the structure, morphology, and surface analyses of individual fuel cell components (e.g., membrane, catalyst, support material, etc.) are used for performance improvement to drastically enhance the power of the respective fuel cell system.

Preparation and Electrochemical Properties of NiCo2O4 Nanospinels Supported on Graphene Derivatives as Earth-Abundant Oxygen Bifunctional Catalysts

This work reports on the facile synthesis and characterisation of a non-precious-metal bifunctional catalyst for oxygen reduction and evolution reactions (ORR and OER). A few-layer reduced graphene oxide-supported NiCo2 O4 catalyst is prepared using a rapid and easy two-step method of synthesis. It consists of the solvothermal poyl(vinylpyrrolidone)-assisted assembly of metal complexes onto few-layer graphene followed by a calcination step aiming at converting metal complexes into the spinel phase. Using this synthesis approach, the most active material demonstrates an outstanding activity towards the OER and ORR, making it one of the best bifunctional catalysts of these reactions ever reported. This composite catalyst exhibits improved bifunctional behaviour with a low reversibility criterion of 746 mV. The ORR process follows a four-electron pathway and the hydroxyl selectivity is higher than those with pure reduced graphene oxide or NiCo2 O4 materials, showing the synergistic effect between the two phases. Moreover, the high activity of this composite catalyst is confirmed by comparing its performance with those obtained on other cobaltite catalysts prepared using a different synthesis method, or those obtained using a different graphene-based support.

Influence of the Atmosphere on Dodecen-1 Isomerization

Abstract In industrial adsorption processes carried out in liquid phase, charges are not always degassed before being injected and so they may contain dissolved oxygen that could induce undesired reactions responsible for premature adsorbent aging. To check this, we compared the reactivity of dodecen-1 in liquid phase at 150°C under air and under argon on two differently active solids, NaY and NaHY-6.7%. It shows that the oxidant atmosphere has a significant influence on the dodecen-1 reactivity. Oxygenated compounds are formed and irreversibly adsorbed on zeolite, leading to the filling of the porosity. This effect is more marked on the less active solid.