Oxysulfides formed by a rare earth and a second metal: II. Shear structures

Many of the oxysulfides containing two metals have layered structures of (RO) sheets and (M_xS_y) sheets (R = rare earth, M = Cu, Ag, Ga, In, Ge, Sn, As, Sb, Bi). In the new compounds (La₄O₃)(AsS₃)₂ and (La₅O₃)In₆S₁₇, parallel ribbons of stoichiometry (La₄O₃) and (La₅O₃) substitute for the (LaO) sheets. The formation of ribbons is explained by shear mechanisms involving two different orientations of the periodic shear planes in the tetragonal (LaO) sheet. In a third compound La₃GaS₅O or (La₂O)LaGaS₅, the formation of (La₂O) ribbons involves similar shear mechanism. All these shear structures preserve the main characters of the layered oxysulfides: oxygen is only bound to lanthanum, and the second metal is only bound to sulfur.     

Resonant mechanisms of inelastic light scattering by low-dimensional electron gases

The contribution of elementary excitations in low-dimensional electron gases to resonant inelastic light scattering is found to be determined by interband transitions involving states at specific wave vectors. In modulation-doped GaAs/GaAlAs quantum wells, we detect only the single-particle excitations (SPE) at resonances with electron-hole transitions at the Fermi wave vector, and only plasmons at resonances with zone-center excitons. The plasmon cross section is comparable to the SPE when double electronic resonance is achieved by tuning the plasmon energy to a valence subband separation.     

Initiator‐Grafted Silica Particles for Controlled Free Radical Polymerization: Influence of the Initiator Structure on the Grafting Density

A series of organic‐inorganic hybrid particles were synthesized by a self‐assembled layer of different initiators, immobilized on silica particles and used for controlled radical polymerization. We use three different initiator systems for atom‐transfer radical polymerization (ATRP), unimolecular nitroxide mediated polymerization (NMP), and bimolecular NMP, for the development of the hybrid inorganic/organic particles. After preliminary qualitative characterization by X‐ray spectroscopy (XPS) and Fourier‐transformed infrared (FT‐IR) measurements, the hybrid nanoparticles were studied by thermogravimetric analysis (TGA) to determine and discuss the initiator graft density in terms of steric hindrance.

The coupling agents employed for the various approaches used here: a) NMP1‐bimolecular system, b) NMP2‐unimolecular system, and c) ATRP.     

Chemical Composition,Antioxidant and Anti-Inflammatory Activities of Clary Sage and Coriander Essential Oils Produced on Polluted and Amended Soils-Phytomanagement Approach

The potential of essential oils (EO), distilled from two aromatic plants—clary sage (Salvia sclarea L.) and coriander (Coriandrum sativum L.)—in view of applications as natural therapeutic agents was evaluated in vitro. These two were cultivated on a trace element (TE)-polluted soil, as part of a phytomanagement approach, with the addition of a mycorrhizal inoculant, evaluated for its contribution regarding plant establishment, growth, and biomass production. The evaluation of EO as an antioxidant and anti-inflammatory, with considerations regarding the potential influence of the TE-pollution and of the mycorrhizal inoculation on the EO chemical compositions, were the key focuses. Besides, to overcome EO bioavailability and target accession issues, the encapsulation of EO in β-cyclodextrin (β-CD) was also assessed. Firstly, clary sage EO was characterized by high proportions of linalyl acetate (51–63%) and linalool (10–17%), coriander seeds EO by a high proportion of linalool (75–83%) and lesser relative amounts of γ-terpinene (6–9%) and α-pinene (3–5%) and coriander aerial parts EO by 2-decenal (38–51%) and linalool (22–39%). EO chemical compositions were unaffected by both soil pollution and mycorrhizal inoculation. Of the three tested EO, the one from aerial parts of coriander displayed the most significant biological effects, especially regarding anti-inflammatory potential. Furthermore, all tested EO exerted promising antioxidant effects (IC₅₀ values ranging from 9 to 38 g L⁻¹). However, EO encapsulation in β-CD did not show a significant improvement of EO biological properties in these experimental conditions. These findings suggest that marginal lands polluted by TE could be used for the production of EO displaying faithful chemical compositions and valuable biological activities, with a non-food perspective.     

Ghost seats in parliaments

In several European Countries citizens’ movements have formed parties whose programme is to reform electoral legislation so that blank votes are transformed into vacant seats in parliament. The first objective of this paper is to offer some tools in order to quantify the potential effect of a reform that would allow citizens to cast a dissatisfaction vote. We show that such a reform would reduce the ease to pass a proposal and modify the distribution of power among parties. The second objective of this paper is to show that this reform could have an impact in parliaments. This is illustrated by the case of the Basque Parliament from 1980 to 2016. At the theoretical level this paper provides some relations between measures of success.     

Sacrificial salts: Compensating the initial charge irreversibility in lithium batteries

Lithium salts enlisting azide, oxocarbons, dicarboxylates and hydrazides have been identified as a practical mean to compensate the irreversible capacity loss of LIBs negative electrodes. During the first charge, the anion loses electrons and converts to gaseous N₂, CO or CO₂, within an acceptable potential range (3 to 4.5 V). We report an electrochemical study on these easily accessible “sacrificial salts”.     

Characterization of lithium alkyl carbonates by X-ray photoelectron spectroscopy: experimental and theoretical study

Lithium alkyl carbonates ROCO2Li result from the reductive decomposition of dialkyl carbonates, which are the organic solvents used in the electrolytes of common lithium-ion batteries. They play a crucial role in the formation of surface layers at the electrode/electrolyte interfaces. In this work, we report on the X-ray photoelectron spectroscopy (XPS) characterization of synthesized lithium methyl and ethyl carbonates. Using Hartree-Fock ab initio calculations, we interpret and simulate the valence spectra of both samples, as well as several other Li alkyl carbonates involved in Li-ion batteries. We show that Li alkyl carbonates can be identified at the electrode's surface by a combined analysis of XPS core peaks and valence spectra.