Numerous additives are used in electrolytes of lithium-ion batteries, especially for the formation of efficient solid electrolyte interphase at the surface of the electrodes. The understanding of the degradation processes of these compounds is thus important. They can be obtained through radiolysis.In the case of fluoroethylene carbonate (FEC), picosecond pulse radiolysis experiments evidenced the formation of FEC •-. This radical is stabilized in neat FEC, whereas the ring opens to form more stable radical anions when FEC is a solute in other solvents, as confirmed by quantum chemistry calculations. In neat FEC, pre-solvated electrons primarily undergo attachment compared to solvation. At long timescales, produced gases (H2, CO, and CO2) were quantified. A reaction scheme for both the oxidizing and reducing pathways at stake in irradiated FEC was proposed. This work evidences that the nature of the primary species formed in FEC depends on the amount of FEC in the solution.
International audienceThe insertion of Single Molecule Magnets (SMMs) in spintronic devices has drawn much attention thanks to their fascinating quantum and classical magnetic properties. Although many efforts have been done in this direction, we are still in search of optimal molecules, which preserve intact the magnetic bistability at the nanoscale. In this frame, we have synthesized a new dysprosium-based dimer characterized by SMM behavior and a double-butterfly-shape hysteresis. The complex has been successfully deposited by sublimation in high vacuum and the peculiar SMM behavior of the complex is fully retained at the nanoscale demonstrating that a modification of the dimer structure aimed for enhancing the SMM character is compatible with nanostructuration purposes
Reaction of hexanuclear octahedral molecular precursors with a 3-chlorobenzoate ligand affords an unprecedented family of isostructural polylanthanide complexes via solvothermal and microwave-assisted syntheses in an acetonitrile medium. The general chemical formula of the compounds that constitute this series is {[Ln(μ-OH)(HO)(NO)(3-cb)]·(CHCN)}, where 3-cb stands for 3-chlorobenzoate and Ln = Eu, Tb, Dy, Ho, Er, or Y. The crystal structure, solubility, and magnetic and luminescent properties of these complexes have been studied. The luminescent properties evidence that the composition of the hexalanthanide precursor is preserved during the synthetic process that is of particular interest for cases in which heterolanthanide complexes are targeted.
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