Search results for "Halide"

showing 10 items of 324 documents

Efficient wide band gap double cation – double halide perovskite solar cells

2017

In this work we study the band gap variation and properties of the perovskite compound Cs0.15FA0.85Pb(BrxI1−x)3 as a function of the halide composition, with the aim of developing an efficient complementary absorber for MAPbI3 in all-perovskite tandem devices. We have found the perovskite stoichiometry Cs0.15FA0.85Pb(Br0.7I0.3)3 to be a promising candidate, thanks to its band gap of approximately 2 eV. Single junction devices using this perovskite absorber lead to a maximum PCE of 11.5%, among the highest reported for solar cells using perovskites with a band gap wider than 1.8 eV.

Materials scienceChemical substanceTandemRenewable Energy Sustainability and the Environmentbusiness.industryBand gapWide-bandgap semiconductorHalideNanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesOptoelectronicsGeneral Materials Science0210 nano-technologyScience technology and societybusinessStoichiometryPerovskite (structure)Journal of Materials Chemistry A
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Charge Transport Layers Limiting the Efficiency of Perovskite Solar Cells: How To Optimize Conductivity, Doping, and Thickness

2019

Perovskite solar cells (PSCs) are one of the main research topics of the photovoltaic community; with efficiencies now reaching up to 24%, PSCs are on the way to catching up with classical inorganic solar cells. However, PSCs have not yet reached their full potential. In fact, their efficiency is still limited by nonradiative recombination, mainly via trap-states and by losses due to the poor transport properties of the commonly used transport layers (TLs). Indeed, state-of-the-art TLs (especially if organic) suffer from rather low mobilities, typically within 10(-5) and 10(-2) cm(-2) V-1 s(-1), when compared to the high mobilities, 1-10 cm(-2) V-1 s(-1), measured for perovskites. This work…

Materials scienceEnergy Engineering and Power TechnologyRECOMBINATIONdopingConductivityperovskite solar cellsCH3NH3PBI3Materials ChemistryElectrochemistryChemical Engineering (miscellaneous)ddc:530Electrical and Electronic EngineeringHYSTERESISMaterialsCèl·lules fotoelèctriquesPerovskite (structure)business.industryPhotovoltaic systemDopingInstitut für Physik und AstronomieCharge (physics)LimitingConductivitat elèctricaHALIDE PEROVSKITEScharge transportHysteresistransport layersOptoelectronicsTIO2conductivitybusiness
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Large area perovskite light-emitting diodes by gas-assisted crystallization:

2019

Halide perovskites have been gaining considerable attention recently for use in light-emitting applications, due to their bandgap tunability, color purity and low cost fabrication methods. However, current fabrication techniques limit the processing to small-area devices. Here, we show that a facile N 2 gas-quenching technique can be used to make methylammonium lead bromide-based perovskite light-emitting diodes (PeLEDs) with a peak luminance of 6600 cd m −2 and a current efficiency of 7.0 cd A −1 . We use this strategy to upscale PeLEDs to large-area substrates (230 cm 2 ) by developing a protocol for slot-die coating combined with gas-quenching. The resulting large area devices (9 device…

Materials scienceFabricationBand gapSlot-die coatings02 engineering and technologySubstrate (electronics)Large area devicesengineering.material010402 general chemistry01 natural sciencesLuminancelaw.inventionCoatinglawQuenchingMaterials ChemistryMaterialsDiodePerovskite (structure)Industrial Innovationbusiness.industryGeneral Chemistry021001 nanoscience & nanotechnologyPerovskite light emitting diodes0104 chemical sciencesLuminanceManufacturing techniquesHalide perovskitesengineeringOptoelectronics0210 nano-technologybusinessLight-emitting diode
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Single-Source Vacuum Deposition of Mechanosynthesized Inorganic Halide Perovskites

2018

Fully inorganic cesium lead halide perovskite thin films were prepared by an easy, fast and dry process based on single-source vacuum deposition. We investigated the structural and optical characteristics of the so-formed films as a function of chemical composition (chloride, bromide and iodide films were formed), post-deposition thermal annealing, as well as previous mechanosynthesis of perovskite powders. We found out that the CsPbX3 perovskite was preferentially formed for the smaller halides and favored by previous ball-milling of CsX and PbX2 precursors. When bigger halides were used and/or CsX and PbX2 precursors were simply mixed without previous mechanosynthesis, PbX2-rich compounds…

Materials scienceGeneral Chemical EngineeringInorganic chemistryHalide02 engineering and technologyGeneral ChemistryQuímica010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesVacuum depositionMaterials Chemistry0210 nano-technologyMaterialsChemistry of Materials
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Cut-edge corrosion of a Zn–55Al-coated steel: A comparison between sulphate and chloride solutions

2011

Abstract Ex situ observations and in situ measurements of current and pH distributions over cut-edge coated steels revealed that Zn–55Al coatings are sacrificial only in chloride solutions, because of an activation of both Zn- and Al-rich phases present in the coating. In sulphate solutions, an efficient cathodic protection occurs only for short times of immersion, because only Zn-rich phases are active in this medium. The low solubility and strong acidification induced by Al(OH)SO4 allows only short distance cathodic protection, but cannot prevent red rust precipitation on the steel surface.

Materials scienceGeneral Chemical EngineeringInorganic chemistryHalideGeneral Chemistryengineering.materialChlorideCorrosionCathodic protectionchemistry.chemical_compoundCoatingchemistrymedicineengineeringGeneral Materials ScienceSolubilitySulfateDissolutionmedicine.drugCorrosion Science
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Colloids of naked CH 3 NH 3 PbBr 3 Perovskite Nanoparticles: Synthesis, Ssability, and thin solid film deposition

2018

A novel preparation of lead halide, CH3NH3PbBr3, perovskite nanoparticle solid films from colloidal "naked" nanoparticles, that is, dispersible nanoparticles without any surfactant, is reported. The colloids are obtained by simply adding potassium ions, whose counterions are both more lipophilic and less coordinating than bromide ions, to the perovskite precursor solutions (CH3NH3Br/PbBr2 in dimethylformamide) following the reprecipitation strategy. The naked nanoparticles exhibit a low tendency to aggregate in solution, and they effectively self-assembled on a substrate by centrifugation of the colloid, leading to homogeneous nanoparticle solid films with arbitrary thickness. These results…

Materials scienceGeneral Chemical EngineeringPHASEHalideNanoparticle02 engineering and technologySubstrate (electronics)INGENIERÍAS Y TECNOLOGÍAS010402 general chemistry01 natural scienceslcsh:ChemistryColloidPhase (matter)//purl.org/becyt/ford/2.10 [https]NANOPARTICLESELECTRON TRANSFERPerovskite (structure)chemistry.chemical_classificationNanotecnologíaGeneral Chemistry021001 nanoscience & nanotechnologyNano-materiales0104 chemical scienceslcsh:QD1-999chemistryChemical engineering//purl.org/becyt/ford/2 [https]LUMINESCENCECounterion0210 nano-technologyLuminescence
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Metallization of the Na 14 Cl 13 Cluster

1994

The structure and energetics of multiple-excess-electron alkali halide clusters Na14Cl14-n, (1 ≤ n ≤ 6) is studied by ab initio calculations using norm-conserving pseudopotentials and local-spin-density-functional theory. Analysis of various electronic properties (Kohn-Sham one-electron eigenvalue spectra, ionization potentials, participation ratios of Kohn-Sham orbitals), as well as multiple F-center formation energies, suggests that these clusters can be characterized as Nan(NaCl)14-n having a "phase-separated" metallic part NaI. The Na14Cl9 (or Na14Cl9+) cluster exhibits a face (surface) segregated metallic Na5 (Na5+) overlayer, the stability of which is demonstrated by a molecular-dynam…

Materials scienceGeneral Physics and AstronomyHalideAlkali metalMolecular physicsSpectral lineOverlayerCondensed Matter::Materials ScienceAtomic orbitalAb initio quantum chemistry methodsIonizationPhysics::Atomic and Molecular ClustersCluster (physics)Physics::Chemical PhysicsAtomic physicsEurophysics Letters (EPL)
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First-principles comparative study of perfect and defective CsPbX3 (X = Br, I) crystals

2020

We thank R. Merkle for numerous fruitful discussions and G. Siegle for experimental assistance. This study was partly supported by the M-ERA-NET project SunToChem (EK). Calculations were performed using computational facilities of St. Petersburg State University and Max Planck Institute for Solid State Research. Open Access funding provided by the Max Planck Society.

Materials scienceGeneral Physics and AstronomyHalideTrimer02 engineering and technologyElectronic structure010402 general chemistry021001 nanoscience & nanotechnologyAlkali metal01 natural sciencesHeat capacitySymmetry (physics)0104 chemical sciencesHybrid functionalChemical physics:NATURAL SCIENCES:Physics [Research Subject Categories]Density functional theoryPhysical and Theoretical Chemistry0210 nano-technology
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Quantifying the Composition of Methylammonium Lead Iodide Perovskite Thin Films with Infrared Spectroscopy

2019

Lead halide perovskites (ABX3) are generally formed from a reaction of the lead halide salt (BX2) with the halide salt of the A cation (AX). The effects of varying film compositions as result of non-stoichiometric precursor ratios on electronic properties of halide perovskites are currently under debate. It is imperative, but experimentally challenging, to determine the chemical composition of thin films as a function of precursor ratio for a full understanding of the effect. Herein we report a precise quantification of the methylammonium (MA) content in differently fabricated films of MAPbI3 via infrared (IR) spectroscopy. We compare the thin film data to the first high quality dielectric …

Materials scienceInfraredAnalytical chemistryInfrared spectroscopyHalideSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyEllipsometryPhysical and Theoretical ChemistryThin filmSpectroscopyChemical compositionPerovskite (structure)The Journal of Physical Chemistry C
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The role of halide ions in the anisotropic growth of gold nanoparticles: a microscopic, atomistic perspective

2016

We provide a microscopic view of the role of halides in controlling the anisotropic growth of gold nanorods through a combined computational and experimental study. Atomistic molecular dynamics simulations unveil that Br− adsorption is not only responsible for surface passivation, but also acts as the driving force for CTAB micelle adsorption and stabilization on the gold surface in a facet-dependent way. The partial replacement of Br− by Cl− decreases the difference between facets and the surfactant density. Finally, in the CTAC solution, no halides or micellar structures protect the gold surface and further gold reduction should be uniformly possible. Experimentally observed nanoparticle'…

Materials scienceInorganic chemistryGeneral Physics and AstronomyHalideNanoparticle02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMicelle0104 chemical sciencesMolecular dynamicsAdsorptionPulmonary surfactantChemical engineeringColloidal goldNanorodPhysical and Theoretical Chemistry0210 nano-technologyPhysical Chemistry Chemical Physics
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