energy related catalysis

by addition of alkali metals as promoters [13] Adding alkali(oxides) to the surface of a transition-metal induces local electrical fields.This allows one to exploit the fact that the N2 dissociation transition state has a larger dipole moment than adsorbed N. Therefore, the scaling relation line in Fig. 1a is shifted downwards resulting in a circumvention of the pure-metal scaling relation and a considerably better catalyst.These industrial advancements can be contrasted to the naturally occurring systems as enzymes including nitrogenase. Despite that this biological system is known to be able to make ammonia at ambient temperatures and pressure, it is a very inefficient process. Hence, not only do we need to find inorganic catalyst but they have to be scalable andmore efficient than the naturally occurring process. The challenge remains to develop a systematic approach to understanding effects like this in order to give us a toolbox of strategies to design radically better catalysts. ACKNOWLEDGEMENT

Catalysis by hybrid sp2/sp3 nanodiamonds and their role in the design of advanced nanocarbon materials

Hybrid sp2/sp3nanocarbons, in particular sp3-hybridized ultra-dispersed nanodiamonds and derivative materials, such as the sp3/sp2-hybridized bucky nanodiamonds and sp2-hybridized onion-like carbons, represent a rather interesting class of catalysts still under consideration

Green Approaches to Carbon Nanostructure-Based Biomaterials

The family of carbon nanostructures comprises several members, such as fullerenes, nano-onions, nanodots, nanodiamonds, nanohorns, nanotubes, and graphene-based materials. Their unique electronic properties have attracted great interest for their highly innovative potential in nanomedicine. However, their hydrophobic nature often requires organic solvents for their dispersibility and processing. In this review, we describe the green approaches that have been developed to produce and functionalize carbon nanomaterials for biomedical applications, with a special focus on the very latest reports

Advanced (photo)electrocatalytic approaches to substitute the use of fossil fuels in chemical production

Electrification of the chemical industry for carbon-neutral production requires innovative (photo)electrocatalysis. This study highlights the contribution and discusses recent research projects in this area, which are relevant case examples to explore new directions but characterised by a little background research effort. It is organised into two main sections, where selected examples of innovative directions for electrocatalysis and photoelectrocatalysis are presented. The areas discussed include (i) new approaches to green energy or H2 vectors, (ii) the production of fertilisers directly from the air, (iii) the decoupling of the anodic and cathodic reactions in electrocatalytic or photoelectrocatalytic devices, (iv) the possibilities given by tandem/paired reactions in electrocatalytic devices, including the possibility to form the same product on both cathodic and anodic sides to “double” the efficiency, and (v) exploiting electrocatalytic cells to produce green H2 from biomass. The examples offer hits to expand current areas in electrocatalysis to accelerate the transformation to fossil-free chemical production

High performance of Au/ZTC based catalysts for the selective oxidation of bio-derivative furfural to 2-furoic acid

Abstract Furfural is a platform bio-molecule for which is valuable to develop new green upgrading processes in biorefinery. We report here for the first time the high performance of Au/ZTC catalyst for the selective oxidation of furfural to 2-furoic acid, as first step to develop electrodes. The ordered nanostructure and high surface area of BEA structure replica ZTC allows to develop 3D-type electrodes. Au/ZTC catalyst shows higher performance than commercial Vulcan, used as reference conductive carbon in fuel cells. The weak acidity on ZTC avoids decarboxylation and esterification reactions, leading to about 90% of furfural conversion fully selectivity to 2-furoic acid

High-Throughput Screening of Heterogeneous Catalysts for the Conversion of Furfural to Bio-Based Fuel Components

The one-pot catalytic reductive etherification of furfural to 2-methoxymethylfuran (furfuryl methyl ether, FME), a valuable bio-based chemical or fuel, is reported. A large number of commercially available hydrogenation heterogeneous catalysts based on nickel, copper, cobalt, iridium, palladium and platinum catalysts on various support were evaluated by a high-throughput screening approach. The reaction was carried out in liquid phase with a 10% w/w furfural in methanol solution at 50 bar of hydrogen. Among all the samples tested, carbon-supported noble metal catalysts were found to be the most promising in terms of productivity and selectivity. In particular, palladium on charcoal catalysts show high selectivity (up to 77%) to FME. Significant amounts of furfuryl alcohol (FA) and 2-methylfuran (2-MF) are observed as the major by-products

On the R&D Landscape Evolution in Catalytic Upgrading of Biomass

International audienceFor the last decade, the scientific community and industrial developers have been searching for improved methods to convert biomass into valuable products in order to respond to enhanced sustainability considerations. In this development, catalysts play an essential role at the core of the many technological routes to convert complex biomass into fuels or chemicals, which can be used in our daily lives. This chapter reports on the evolution of catalytic conversion of biomass by exploring databases on scientific literature and on patents retrieved from Scopus and DWPI. The trend analysis of more than 14,000 patent and nonpatent documents on renewable biological feedstock conversion by catalytic route has been carried out by using Intellixir, a statistical tool to analyze a large number of data for scientific intelligence. The scope of this chapter is to not only display a comprehensive study on patent and nonpatent literature in the catalytic upgrading (value creation) of biomass, but to increase the awareness in the use of patent literature as a tool to reach the rich and open-source treasure of knowledge in various technological fields

Dynamics at polarized carbon dioxide-iron oxyhydroxide interfaces unveil the origin of multicarbon product formation

Surface-sensitive ambient pressure X-ray photoelectron spectroscopy and near-edge X-ray absorption fine structure spectroscopy combined with an electrocatalytic reactivity study, multilength-scale electron microscopy, and theoretical modeling provide insights into the gas-phase selective reduction of carbon dioxide to isopropanol on a nitrogen-doped carbon-supported iron oxyhydroxide electrocatalyst. Dissolved atomic carbon forms at relevant potentials for carbon dioxide reduction from the reduction of carbon monoxide chemisorbed on the surface of the ferrihydrite-like phase. Theoretical modeling reveals that the ferrihydrite structure allows vicinal chemisorbed carbon monoxide in the appropriate geometrical arrangement for coupling. Based on our observations, we suggest a mechanism of three-carbon-atom product formation, which involves the intermediate formation of atomic carbon that undergoes hydrogenation in the presence of hydrogen cations upon cathodic polarization. This mechanism is effective only in the case of thin ferrihydrite-like nanostructures coordinated at the edge planes of the graphitic support, where nitrogen edge sites stabilize these species and lower the overpotential for the reaction. Larger ferrihydrite-like nanoparticles are ineffective for electron transport

Interfacial chemistry in the electrocatalytic hydrogenation of CO2 over C‑supported Cu-based systems

Operando soft and hard X-ray spectroscopic techniques were used in combination with plane-wave density functional theory (DFT) simulations to rationalize the enhanced activities of Zn-containing Cu nanostructured electrocatalysts in the electrocatalytic CO2 hydrogenation reaction. We show that at a potential for CO2 hydrogenation, Zn is alloyed with Cu in the bulk of the nanoparticles with no metallic Zn segregated; at the interface, low reducible Cu­(I)–O species are consumed. Additional spectroscopic features are observed, which are identified as various surface Cu­(I) ligated species; these respond to the potential, revealing characteristic interfacial dynamics. Similar behavior was observed for the Fe–Cu system in its active state, confirming the general validity of this mechanism; however, the performance of this system deteriorates after successive applied cathodic potentials, as the hydrogen evolution reaction then becomes the main reaction pathway. In contrast to an active system, Cu­(I)–O is now consumed at cathodic potentials and not reversibly reformed when the voltage is allowed to equilibrate at the open-circuit voltage; rather, only the oxidation to Cu­(II) is observed. We show that the Cu–Zn system represents the optimal active ensembles with stabilized Cu­(I)–O; DFT simulations rationalize this observation by indicating that Cu–Zn–O neighboring atoms are able to activate CO2, whereas Cu–Cu sites provide the supply of H atoms for the hydrogenation reaction. Our results demonstrate an electronic effect exerted by the heterometal, which depends on its intimate distribution within the Cu phase and confirms the general validity of these mechanistic insights for future electrocatalyst design strategies