Search results for "shell"

showing 10 items of 748 documents

Manganese speciation inDiplodon chilensis patagonicusshells: a XANES study

2009

X-ray absorption near-edge spectroscopy (XANES) at the Mn K-edge was used to investigate the environment of Mn in situ within the growth increments of the long-lived freshwater bivalve species Diplodon chilensis patagonicus. Single XANES spectra and Mn Kalpha fluorescence distributions were acquired at submillimetre resolution (up to 100 microm x 50 microm), at Mn concentrations below the weight percent range (100-1000 microg g(-1)) in a high Ca matrix. The position and intensity of the pre-edge feature in the shell spectrum resembles best that of the Mn(II)-bearing reference compounds, suggesting that this is the oxidation state of Mn in the bivalve shells. By comparison with the XANES spe…

ManganeseNuclear and High Energy PhysicsRadiationFreshwater bivalveChemistrymedia_common.quotation_subjectAnalytical chemistrychemistry.chemical_elementManganeseXANESBivalviaMetalSpeciationX-Ray Absorption SpectroscopyOxidation statevisual_artvisual_art.visual_art_mediumAnimalsBivalve shellSpectroscopyInstrumentationmedia_commonJournal of Synchrotron Radiation
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Aquaculture and its by-products as a source of nutrients and bioactive compounds

2020

Underutilized marine resources (e.g., algae, fish, and shellfish processing by-products), as sustainable alternatives to livestock protein and interesting sources of bioactive compounds, have attracted the attention of the researchers. Aquatic products processing industries are growing globally and producing huge amounts of by-products that often discarded as waste. However, recent studies pointed out that marine waste contains several valuable components including high-quality proteins, lipids, minerals, vitamins, enzymes, and bioactive compounds that can be used against cancer and some cardiovascular disorders. Besides, previously conducted studies on algae have shown the presence of some…

Marine conservation0303 health sciences030309 nutrition & dieteticsbusiness.industrySeafood processingBiologybiology.organism_classificationBiotechnology03 medical and health sciencesNutrientAlgaeAquacultureFish <Actinopterygii>businessFish processingShellfish
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Multiple points of view of heteronuclear NOE: long range vs short range contacts in pyrrolidinium based ionic liquids in the presence of Li salts.

2015

The nuclear Overhauser enhancement (NOE) is a powerful tool of NMR spectroscopy extensively used to gain structural information in ionic liquids (ILs). A general model for the distance dependence of intermolecular NOE in ILs was recently proposed showing that NOE spots beyond the first solvation shell and accounts for long-range effects. This conclusion prompted for a deep rethinking of the NOE data interpretation in ILs. In this paper we present an extensive and quantitative study of N-propyl-N-methyl pyrrolidinium bis(trifluoromethanesulfonyl)imide (PYR13TFSI), the homologue with bis(fluorosulfonyl)imide (PYR13FSI), and their mixtures with LiTFSI based on 1H-19F and 1H-7LiNOE correlation …

Materials Chemistry2506 Metals and AlloysAtomic and Molecular Physics and OpticAnalytical chemistryCondensed Matter PhysicIonic liquidLithiumchemistry.chemical_compoundMaterials ChemistryPhysical and Theoretical ChemistryImideHeteronuclear NOESpectroscopyIntermolecular NOE;Fluorosulfonylimide;Ionic liquids;NMR;Trifluoromethanesulfonimide;Pyrrolidinium;Lithium;Heteronuclear NOELarmor precessionFluorosulfonylimideIntermolecular NOEElectronic Optical and Magnetic MaterialIntermolecular forceHeteronuclear NOE NMR Ionic liquids Pyrrolidinium Fluorosulfonylimide Trifluoromethanesulfonimide Lithium Intermolecular NOENuclear magnetic resonance spectroscopyCondensed Matter PhysicsAtomic and Molecular Physics and OpticsNMRElectronic Optical and Magnetic MaterialsIonic liquidsCrystallographyTrifluoromethanesulfonimideSolvation shellHeteronuclear moleculechemistryIonic liquidPolarPyrrolidinium
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Structural and luminescence properties of amorphous SiO2 nanoparticles

2011

We report an experimental study on the photoluminescence band peaked at 2.7 eV (blue band) induced by thermal treatments in nanometric amorphous SiO 2. In particular the emission dependence on the nanometric particles size as a function of their mean diameter from 7 nm up to 40 nm is investigated. We found that the emission amplitude increases on decreasing the particle diameter, showing a strong correlation between the blue band and the nanometric nature of the particles. By Raman spectroscopy measurements it is evidenced that the SiO2 nanoparticles matrix is significantly affected by the reduction of size. Basing on the shell-like model, these findings are interpreted assuming that the de…

Materials Chemistry2506 Metals and AlloysPhotoluminescenceMaterials scienceShell (structure)Analytical chemistryNanoparticleCeramics and CompositeSilica nanoparticleCondensed Matter PhysicMolecular physicssymbols.namesakeMaterials ChemistryPoint-defectRamannanoparticelle di silice difetti di punto fotoluminescenzaElectronic Optical and Magnetic MaterialSettore FIS/01 - Fisica SperimentaleTime-resolved luminescenceCondensed Matter PhysicsCrystallographic defectElectronic Optical and Magnetic MaterialsAmorphous solidCeramics and CompositessymbolsParticle sizeRaman spectroscopyLuminescence
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Cubic aromaticity in ligand-stabilized doped Au superatoms

2021

The magnetic response of valence electrons in doped gold-based [M@Au8L8]q superatoms (M = Pd, Pt, Ag, Au, Cd, Hg, Ir, and Rh; L = PPh3; and q = 0, +1, +2) is studied by calculating the gauge including magnetically induced currents (GIMIC) in the framework of the auxiliary density functional theory. The studied systems include 24 different combinations of the dopant, total cluster charge, and cluster structure (cubic-like or oblate). The magnetically induced currents (both diatropic and paratropic) are shown to be sensitive to the atomic structure of clusters, the number of superatomic electrons, and the chemical nature of the dopant metal. Among the cubic-like structures, the strongest arom…

Materials science010304 chemical physicsDopantdouppaus (puolijohdetekniikka)SuperatomGeneral Physics and AstronomyAromaticityElectronic structure010402 general chemistry01 natural scienceskulta0104 chemical sciencesNanoclustersklusteritCrystallography0103 physical sciencesnanohiukkasetDensity functional theoryPhysical and Theoretical ChemistryValence electronOpen shellThe Journal of Chemical Physics
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Ultrafast Charge Separation at the CdSe/CdS Core/Shell Quantum Dot/Methylviologen Interface: Implications for Nanocrystal Solar Cells

2011

Exciton separation dynamics in the electron transfer system containing highly photostable CdSe/CdS core/shell nanocrystal quantum dots and adsorbed methylviologen was investigated by means of femtosecond absorption spectroscopy. The experiments revealed that electron extraction from the photoexcited core is possible, and the rate of the ET reaction strongly depends on the CdS shell thickness. A CdS associated exponential decay constant β of 0.33 A−1 was obtained reflecting the electronic barrier effect of the shell. These findings show that core/shell structures are well suited for the design of optimized QD-based solar cells.

Materials scienceAbsorption spectroscopyExcitonShell (structure)ElectronQuantum dot solar cellCondensed Matter::Mesoscopic Systems and Quantum Hall EffectSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceElectron transferGeneral EnergyNanocrystalChemical physicsQuantum dotPhysics::Atomic and Molecular ClustersPhysical and Theoretical ChemistryAtomic physicsThe Journal of Physical Chemistry C
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Synthesis and characterization of GaN/ReS2, ZnS/ReS2 and ZnO/ReS2 core/shell nanowire heterostructures

2020

This research was funded by the ERDF project “Smart Metal Oxide Nanocoatings and HIPIMS Technology”, project number: 1.1.1.1/18/A/073. Institute of Solid State Physics, University of Latvia as the Center of Excellence has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement No. 739508, project CAMART².

Materials scienceAbsorption spectroscopyNanowireGeneral Physics and Astronomy02 engineering and technology010402 general chemistry01 natural sciences7. Clean energylaw.inventionlawMonolayer:NATURAL SCIENCES:Physics [Research Subject Categories]Layered materialsElectron microscopyX-ray absorption spectroscopyReS2business.industryGrapheneX-ray absorption spectroscopyHeterojunctionSurfaces and InterfacesGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsX-ray diffraction0104 chemical sciencesSurfaces Coatings and FilmsSemiconductorRaman spectroscopyCore-shell nanowireOptoelectronicsDirect and indirect band gaps0210 nano-technologybusinessApplied Surface Science
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Silica nanoparticle core structure examined by the E?Si? center 29Si strong hyperfine interaction

2015

Abstract β-Ray irradiation up to 1.2 GGy was employed to induce E′Si γ defects and to study the structure of silica nanoparticles with diameters from 7 up to 20 nm. Defect concentration and their 29 Si strong hyperfine doublet were investigated through electron paramagnetic resonance measurements. Our data indicate that stable defects are located in the nanoparticle core. Furthermore, the E′Si γ hyperfine interaction evidences that the core structure is denser than bulk silica and independent from the particle size. Finally, we put in evidence that the core structure is stable and unaffected by the irradiation in the investigated dose range maintaining the specific features of nanoparticles.

Materials scienceAnalytical chemistryNanoparticleSilica nanoparticleCeramics and CompositeCondensed Matter PhysicMaterials Chemistry Metals and Alloyslaw.inventionSilica nanoparticleslawMaterials ChemistryIrradiationElectron paramagnetic resonanceHyperfine structureComputingMilieux_MISCELLANEOUSRange (particle radiation)Core-shell modelElectronic Optical and Magnetic MaterialSettore FIS/01 - Fisica Sperimentaleβ-Ray irradiation[CHIM.MATE]Chemical Sciences/Material chemistryCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCore (optical fiber)Chemical physicsCeramics and CompositesParticle sizeElectron paramagnetic resonance
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Co-crystallization of atomically precise metal nanoparticles driven by magic atomic and electronic shells

2018

This paper reports co-crystallization of two atomically precise, different-size ligand-stabilized nanoclusters, a spherical (AuAg)267(SR)80 and a smaller trigonal-prismatic (AuAg)45(SR)27(PPh3)6 in 1:1 ratio, characterized fully by X-ray crystallographic analysis (SR = 2,4-SPhMe2). The larger cluster has a four concentric-shell icosahedral structure of Ag@M12@M42@M92@Ag120(SR)80 (M = Au or Ag) with the inner-core M147 icosahedron observed here for metal nanoparticles. The cluster has an open electron shell of 187 delocalized electrons, fully metallic, plasmonic behavior, and a zero HOMO-LUMO energy gap. The smaller cluster has an 18-electron shell closing, a notable HOMO-LUMO energy gap and…

Materials scienceBand gapIcosahedral symmetryScienceElectron shellGeneral Physics and Astronomy02 engineering and technology010402 general chemistry01 natural sciencesGeneral Biochemistry Genetics and Molecular BiologyArticleNanoclustersco-crystallizationDelocalized electronAtomCluster (physics)Physics::Atomic and Molecular Clustersmetal nanoparticleslcsh:SciencePlasmonMultidisciplinaryQGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesChemical physicslcsh:Qnanohiukkaset0210 nano-technologyNature Communications
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Pressure effects on the electronic and optical properties ofAWO4wolframites (A =Cd, Mg, Mn, and Zn): The distinctive behavior of multiferroic MnWO4

2012

The electronic band-structure and band-gap dependence on the $d$ character of ${A}^{2+}$ cation in $A$WO${}_{4}$ wolframite-type oxides is investigated for different compounds ($A$ $=$ Mg, Zn, Cd, and Mn) by means of optical-absorption spectroscopy and first-principles density-functional calculations. High pressure is used to tune their properties up to 10 GPa by changing the bonding distances establishing electronic to structural correlations. The effect of unfilled $d$ levels is found to produce changes in the nature of the band gap as well as its pressure dependence without structural changes. Thus, whereas Mg, Zn, and Cd, with empty or filled $d$ electron shells, give rise to direct and…

Materials scienceBand gapbusiness.industryAnalytical chemistryElectron shellCondensed Matter PhysicsPressure coefficientElectronic Optical and Magnetic MaterialsSemiconductorDirect and indirect band gapsMultiferroicsAbsorption (logic)SpectroscopybusinessPhysical Review B
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