Nitrurs i oxinitrurs de metalls de transició amb estructura antifluorita : síntesi, caraterització i aplicació en bateries de liti /

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Importancia del bienestar animal en la decisión de compra de carne fresca de cerdo

Actualmente en España el nivel de bienestar animal en la producción de cerdos es bajo, ya que al nacer los cerdos se les castra sin anestesia, causando gran dolor al animal. En España se castran 8 millones de cerdos al año, principalmente para mejorar la calidad de la carne, pero también para facilitar el manejo de los mismos. Si los granjeros castraran a los animales con anestesia implicaría costes de producción más elevados al tener que costear el material médico, y el bienestar de los cerdos sería medio, asimismo, no castrar a los cerdos implica que la carne de éstos desarrolla un sabor y un olor característico que puede ser desagradable para algunas personas, pero el bienestar del animal sería alto, ya que no alteramos su estado natural de vida. Con este trabajo se pretende analizar el comportamiento y actitudes de los consumidores hacia el consumo de la carne fresca de cerdo. Asimismo, investigar el conocimiento que tienen las personas sobre la castración y el bienestar animal, y si estarían dispuestos a pagar un precio más alto en la carne para favorecer el bienestar de los animales sacrificados. Para conseguir este objetivo, se ha diseñado un cuestionario, que se realizó para 100 consumidores en Barcelona. Los resultados obtenidos demuestran que aunque la carne de cerdo fresca es una de las más consumidas con diferencia, la mayoría de los consumidores no tienen conocimientos suficientes acerca del bienestar animal, siendo uno de los atributos menos tenido en cuenta a la hora de hacer la compra

Visualization of electrochemical reactions in battery materials with X-ray microscopy and mapping

Unlocking the full performance capabilities of battery materials will require a thorough understanding of the underlying electrochemical mechanisms at a variety of length scales. A broad arsenal of X-ray microscopy and mapping techniques is now available to probe these processes down to the nanoscale. The tunable nature of X-ray sources allows for the extraction of chemical states through spectromicroscopy. The addition of phase contrast imaging can retrieve the complex-valued refraction of the material, giving an even more nuanced chemical picture. Tomography and coherent Bragg diffraction imaging provide a reconstructed three-dimensional volume of the specimen, as well as internal strain information from the latter. Many recent insights into battery materials have been achieved through the creative use of these, and similar, methods. Experiments performed while the battery is being actively cycled reveal behavior that differs significantly from what is observed at equilibrium and metastable conditions. Planned improvements to X-ray source brightness and coherence will extend these techniques by alleviating the current trade-off in time, chemical, and spatial resolutio

Structural Evolution of Layered Manganese Oxysulfides during Reversible Electrochemical Lithium Insertion and Copper Extrusion.

The electrochemical lithiation and delithiation of the layered oxysulfide Sr2MnO2Cu4-δS3 has been investigated by using a combination of in situ powder X-ray diffraction and ex situ neutron powder diffraction, X-ray absorption and 7Li NMR spectroscopy, together with a range of electrochemical experiments. Sr2MnO2Cu4-δS3 consists of [Sr2MnO2] perovskite-type cationic layers alternating with highly defective antifluorite-type [Cu4-δS3] (δ ≈ 0.5) anionic layers. It undergoes a combined displacement/intercalation (CDI) mechanism on reaction with Li, where the inserted Li replaces Cu, forming Li4S3 slabs and Cu+ is reduced and extruded as metallic particles. For the initial 2-3% of the first discharge process, the vacant sites in the sulfide layer are filled by Li; Cu extrusion then accompanies further insertion of Li. Mn2.5+ is reduced to Mn2+ during the first half of the discharge. The overall charging process involves the removal of Li and re-insertion of Cu into the sulfide layers with re-oxidation of Mn2+ to Mn2.5+. However, due to the different diffusivities of Li and Cu, the processes operating on charge are quite different from those operating during the first discharge: charging to 2.75 V results in the removal of most of the Li, little reinsertion of Cu, and good capacity retention. A charge to 3.75 V is required to fully reinsert Cu, which results in significant changes to the sulfide sublattice during the following discharge and poor capacity retention. This detailed structure-property investigation will promote the design of new functional electrodes with improved device performance

Visualization of the Phase Propagation within Carbon-Free Li4Ti5O12 Battery Electrodes

The electrochemical reactions occurring in batteries involve the transport of ions and electrons among the electrodes, the electrolyte, and the current collector. In Li-ion battery electrodes, this dual functionality is attained with porous composite electrode structures that contain electronically conductive additives. Recently, the ability to extensively cycle composite electrodes of Li4Ti5O12without any conductive additives generated questions about how these structures operate, the answers to which could be used to design architectures with other materials that reduce the amount of additives that do not directly store energy. Here, the changes occurring in carbon-free Li4Ti5O12 electrodes during lithiation were studied by a combination of ex situ and operando optical microscopy and microbeam X-ray absorption spectroscopy (μ-XAS). The measurements provide visualizations of the percolation of lithiated domains through the thick (∼40-μm) structure after a depth of discharge of only 1%, followed by a second wave of propagation starting with regions in closest contact with the current collector and progressing toward regions in contact with the bulk electrode. These results emphasize the interplay between the electronic and ionic conductivities of the phases involved in a battery reaction and the formation of the phases in localized areas in the electrode architecture. They provide new insights that could be used to refine the design of these architectures to minimize transport limitations while maximizing energy density

Transcriptomic and genetic studies identify NFAT5 as a candidate gene for cocaine dependence

Cocaine reward and reinforcing effects are mediated mainly by dopaminergic neurotransmission. In this study, we aimed at evaluating gene expression changes induced by acute cocaine exposure on SH-SY5Y-differentiated cells, which have been widely used as a dopaminergic neuronal model. Expression changes and a concomitant increase in neuronal activity were observed after a 5 μM cocaine exposure, whereas no changes in gene expression or in neuronal activity took place at 1 μM cocaine. Changes in gene expression were identified in a total of 756 genes, mainly related to regulation of transcription and gene expression, cell cycle, adhesion and cell projection, as well as mitogen-activeated protein kinase (MAPK), CREB, neurotrophin and neuregulin signaling pathways. Some genes displaying altered expression were subsequently targeted with predicted functional single-nucleotide polymorphisms (SNPs) in a case-control association study in a sample of 806 cocaine-dependent patients and 817 controls. This study highlighted associations between cocaine dependence and five SNPs predicted to alter microRNA binding at the 3′-untranslated region of the NFAT5 gene. The association of SNP rs1437134 with cocaine dependence survived the Bonferroni correction for multiple testing. A functional effect was confirmed for this variant by a luciferase reporter assay, with lower expression observed for the rs1437134G allele, which was more pronounced in the presence of hsa-miR-509. However, brain volumes in regions of relevance to addiction, as assessed with magnetic resonance imaging, did not correlate with NFAT5 variation. These results suggest that the NFAT5 gene, which is upregulated a few hours after cocaine exposure, may be involved in the genetic predisposition to cocaine dependence

Structure and Sodium Ion Dynamics in Sodium Strontium Silicate Investigated by Multinuclear Solid-State NMR

© 2016 American Chemical Society.The high oxide ion conductivity of the proposed sodium strontium silicate ion conductors Sr0.55Na0.45SiO2.775 (>10-2 S·cm-1 at 525 °C) and its unusual alkali metal substitution strategy have been extensively questioned in the literature. Here, we present a comprehensive understanding of the structure of this material using a combination of XRD and multinuclear 17O, 23Na, and 29Si solid-state NMR spectroscopy data and a detailed investigation of the Na ion dynamics by high temperature 23Na NMR line shape analysis and relaxation rates measurements. Both 23Na and 29Si NMR spectra demonstrate the absence of Na doping in strontium silicate SrSiO3 and the presence of an amorphous phase identified as Na2O·2SiO2 glass as the Na-containing product. Devitrification at 800 °C yields crystallization of the Na2O·2SiO2 glass into the known crystalline α-Na2Si2O5 phase which was positively identified by its XRD pattern and the extensive and clear 17O, 23Na, and 29Si NMR fingerprints. High temperature 23Na NMR reveals that the Na ions are mobile in the Na2O·2SiO2 amorphous component below its glass transition temperature (∼450 °C). In contrast, 23Na NMR data obtained on the crystalline α-Na2Si2O5 shows limited Na dynamics below ∼650 °C, and this result explains the large discrepancy in the conductivity observed in the literature which strongly depends on the thermal history of the Sr0.55Na0.45SiO2.775 material. These insights demonstrate that the high conductivity observed in Sr0.55Na0.45SiO2.775 is due to Na conduction in the Na2O·2SiO2 glass, and this motivates the quest for the discovery of low temperature fast ion conductors in noncrystalline solids

Three-dimensional localization of nanoscale battery reactions using soft X-ray tomography.

Battery function is determined by the efficiency and reversibility of the electrochemical phase transformations at solid electrodes. The microscopic tools available to study the chemical states of matter with the required spatial resolution and chemical specificity are intrinsically limited when studying complex architectures by their reliance on two-dimensional projections of thick material. Here, we report the development of soft X-ray ptychographic tomography, which resolves chemical states in three dimensions at 11 nm spatial resolution. We study an ensemble of nano-plates of lithium iron phosphate extracted from a battery electrode at 50% state of charge. Using a set of nanoscale tomograms, we quantify the electrochemical state and resolve phase boundaries throughout the volume of individual nanoparticles. These observations reveal multiple reaction points, intra-particle heterogeneity, and size effects that highlight the importance of multi-dimensional analytical tools in providing novel insight to the design of the next generation of high-performance devices

Cycling of block copolymer composites with lithium-conducting ceramic nanoparticles

Solid polymer and perovskite-type ceramic electrolytes have both shown promise in advancing solid-state lithium metal batteries. Despite their favorable interfacial stability against lithium metal, polymer electrolytes face issues due to their low ionic conductivity and poor mechanical strength. Highly conductive and mechanically robust ceramics, on the other hand, cannot physically remain in contact with redox-active particles that expand and contract during charge-discharge cycles unless excessive pressures are used. To overcome the disadvantages of each material, polymer-ceramic composites can be formed; however, depletion interactions will always lead to aggregation of the ceramic particles if a homopolymer above its melting temperature is used. In this study, we incorporate Li0.33La0.56TiO3 (LLTO) nanoparticles into a block copolymer, polystyrene-b-poly (ethylene oxide) (SEO), to develop a polymer-composite electrolyte (SEO-LLTO). TEMs of the same nanoparticles in polyethylene oxide (PEO) show highly aggregated particles whereas a significant fraction of the nanoparticles are dispersed within the PEO-rich lamellae of the SEO-LLTO electrolyte. We use synchrotron hard x-ray microtomography to study the cell failure and interfacial stability of SEO-LLTO in cycled lithium-lithium symmetric cells. Three-dimensional tomograms reveal the formation of large globular lithium structures in the vicinity of the LLTO aggregates. Encasing the SEO-LLTO between layers of SEO to form a “sandwich” electrolyte, we prevent direct contact of LLTO with lithium metal, which allows for the passage of seven-fold higher current densities without signatures of lithium deposition around LLTO. We posit that eliminating particle clustering and direct contact of LLTO and lithium metal through dry processing techniques is crucial to enabling composite electrolytes