Littérature scientifique sur le sujet « Ruthenium phosphide nanoparticles »

The development of scalable hydrogen production technology to produce hydrogen economically and in an environmentally friendly way is particularly important. The hydrogen evolution reaction (HER) is a clean, renewable, and potentially cost-effective pathway to produce hydrogen, but it requires the use of a favorable electrocatalyst which can generate hydrogen with minimal overpotential for practical applications. Up to now, ruthenium phosphide Ru2P has been considered as a high-performance electrocatalyst for the HER. However, a tedious post-treatment method as well as large consumption of solvents in conventional solution-based synthesis still limits the scalable production of Ru2P electrocatalysts in practical applications. In this study, we report a facile and cost-effective strategy to controllably synthesize uniform ultrasmall Ru2P nanoparticles embedded in carbon for highly efficient HER. The key to our success lies in the use of a solid-state ball milling-assisted technique, which overcomes the drawbacks of the complicated post-treatment procedure and large solvent consumption compared with solution-based synthesis. The obtained electrocatalyst exhibits excellent Pt-like HER performance with a small overpotential of 36 mV at current density of 10 mA cm−2 in 1 M KOH, providing new opportunities for the fabrication of highly efficient HER electrocatalysts in real-world applications.

Selective deuteration of phenyl rings in phenyl-alkyl phosphines, including diphosphines, was achieved using Ru/PVP nanoparticles and D₂, which enables the comprehension of how different phosphorus ligands coordinate to the nanoparticle surface.

Phosphorus chemistry is a very broad field with a great range of applications. The goals of this Ph.D. thesis are related to different aspects of low-valent phosphorus chemistry: going from the synthesis of fluorophosphine ligands through a “green” and innovative pathway, to the activation and functionalization of elemental white phosphorus in the presence of late transition metals, and, finally, to the not yet explored synthesis of ruthenium phosphide nanoparticles starting from white phosphorus. In Chapter 1, different points related to the phosphorus chemistry are mentioned. The opening section reports a general description of the element phosphorus and its allotropic modifications before taking into detailed consideration the reactivity of white phosphorus, emphasizing on the production of organophosphorus compounds through catalytic processes involving the activation of P4 mediated by transition metal complexes. The second section depicts a brief introduction about the importance of phosphine ligands in catalysis, particularly giving attention to the role of fluorophosphine ligands. Finally, the last section deals with the synthesis of metal phosphides nanoparticles, which are of great interest on diverse fields, particularly in catalysis, aiming at P4-derived metal phosphide nanoparticles. Chapter 2 describes the study of the transformation of phosphorous oxyacids, such as PhPO(OH)H, H3PO3, H3PO2, into the corresponding fluorophosphines mediated by [CpRu(PPh3)2Cl] under mild reaction conditions using a soft deoxyfluorinating agent, commercially available as XtalFluor-E. The reaction is selective, proceeds with high yields and can be extended to a wide range of phosphorous oxyacids once coordinated to the ruthenium fragment {CpRu(PPh3)2}+ as their hydroxyphosphine tautomer. Deoxyfluorination of phenylphosphinic acid was also mediated by [CpRRu(CH3CN)3]PF6, where CpR: Cp = C5H5, Cp* = C5Me5, and {η6-(p-cymene)Ru(µ-Cl)Cl}2. On chapter 3, the coordination chemistry of white phosphorus towards a 16 electron ruthenium organometallic complex [Cp*RuPCy3X], where Cp* = C5Me5, X = Cl, Br, I is described. The different electronegativity and steric bulk in the series of halogens changes the reactivity with white phosphorus. Migration of the halogen from ruthenium to the P4 moiety was observed, in the case of chloride and bromide, obtaining bimetallic complexes bearing unexpected P4X2 (X = Cl, Br) moiety as bridging ligands. In the case of iodide, a completely different structure is proposed, containing the not yet previously reported P4I ligand as a bridging moiety between two Ru(II) centers. Chapter 4 deals with the synthesis and characterization of ruthenium phosphide nanoparticles using white phosphorus as P-source. The novelty introduced is the use of white phosphorus as phosphorus source to react with previously prepared ruthenium nanoparticles. A preliminary catalytic study on hydrogenation of phenylacetylene under mild conditions shows very good catalytic activity and selectivity towards the fully hydrogenated product, ethylbenzene.