Search results for "quantum yield"

showing 10 items of 163 documents

Continuous-Flow Synthesis of Orange Emitting Sn(II)-Doped CsBr Materials

2021

An ongoing demand toward lead-free all-inorganic cesium metal halide perovskites has presented Sn(II) as an ideal substitute of Pb(II) for applications in optoelectronic devices. The major concern regarding Sn(II) is the instability due to the ambient oxidation to Sn(IV). To expand the scope of traditional perovskite and analogues, herein the synthesis and optical performance of Sn(II)-doped CsBr, a new material formed by interstitial doping of Sn(II) into the CsBr matrix, are reported for the first time. This material is prepared following an antisolvent mediated recrystallization method using a continuous flow reactor, which is beneficial for scaling up the production compared to traditio…

PhotoluminescenceRecrystallization (geology)Materials scienceAnalytical chemistrychemistry.chemical_elementHalideQuantum yield02 engineering and technology010402 general chemistry7. Clean energy01 natural sciencescontinuous flow reactor synthesis CsBr interstitial doping long-term ambient stability photoluminescence quantum yield self-trapped excitonic emissionMetalphotoluminescence quantum yieldlong-term ambient stabilityself-trapped excitonic emissionPerovskite (structure)Dopingcontinuous flow reactor synthesis021001 nanoscience & nanotechnologyAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialschemistryvisual_artCaesiumvisual_art.visual_art_mediumCsBrinterstitial doping0210 nano-technology
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Synthesis and Characterization of Highly Luminescent CdSe—Core CdS/Zn0.5Cd0.5S/ZnS Multishell Nanocrystals.

2005

We report on the preparation and structural characterization of CdSe nanocrystals, which are covered by a multishell structure from CdS and ZnS. By using the newly developed successive ion layer adhesion and reaction (SILAR) technique, we could gradually change the shell composition from CdS to ZnS in the radial direction. Because of the stepwise adjustment of the lattice parameters in the radial direction, the resulting nanocrystals show a high crystallinity and are almost perfectly spherical, as was investigated by X-ray diffraction and electron microscopy. Also, due to the radial increase of the respective valence- and conduction-band offsets, the nanocrystals are well electronically pas…

PhotoluminescenceValence (chemistry)ChemistryInorganic chemistryQuantum yieldGeneral ChemistryGeneral MedicineColloidal crystalBiochemistryCatalysisIonChalcogenCrystallinityColloidColloid and Surface ChemistryNanocrystalChemical engineeringLuminescenceChemInform
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Dibenzo[hi,st]ovalene as Highly Luminescent Nanographene: Efficient Synthesis via Photochemical Cyclodehydroiodination, Optoelectronic Properties, an…

2019

Dibenzo[hi,st]ovalene (DBOV), as a new nanographene, has demonstrated promising optical properties, such as red emission with a high fluorescence quantum yield of 79% and stimulated emission, as well as high thermal stability and photostability, which indicated its promise as a light-emitting and optical gain material. However, the previous synthetic routes required at least 12 steps. This obstructed access to different derivatives, e.g., to obtain crystals suitable for X-ray diffraction analysis and to tune the optoelectronic properties. Here, we report an efficient synthetic pathway to DBOV based on a sequential iodination-benzannulation of bi(naphthylphenyl)diyne, followed by photochemic…

Photon antibunchingbusiness.industryChemistryQuantum yieldGeneral ChemistryOvalene010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisFluorescence spectroscopy0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryIntersystem crossingOptoelectronicsStimulated emissionEmission spectrumbusinessSpectroscopyJournal of the American Chemical Society
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Unraveling exciton dynamics in amorphous silicon dioxide: Interpretation of the optical features from 8 to 11 eV.

2011

Physical review / B 83, 174201 (2011). doi:10.1103/PhysRevB.83.174201

PhysicsCoupling constantAbsorption spectroscopyPhononExcitonSettore FIS/01 - Fisica SperimentaleQuantum yieldCondensed Matter Physics530Exciton dynamicElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceDelocalized electronamorphous silicon dioxideLattice (order)ddc:530absorption and reflectivity spectraAtomic physicsElectronic band structure
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In situobservation of the formation, diffusion, and reactions of hydrogenous species inF2-laser-irradiatedSiO2glass using a pump-and-probe technique

2006

We quantitatively studied the formation, diffusion, and reactions of mobile interstitial hydrogen atoms $({\mathrm{H}}^{0})$ and molecules $({\mathrm{H}}_{2})$ in ${\mathrm{F}}_{2}$-laser-irradiated silica $(\mathrm{Si}{\mathrm{O}}_{2})$ glass between 10 and $330\phantom{\rule{0.3em}{0ex}}\mathrm{K}$. Two key techniques were used: single-pulse ${\mathrm{F}}_{2}$ laser photolysis of silanol (SiOH) groups to selectively create pairs of ${\mathrm{H}}^{0}$ and oxygen dangling bonds (nonbridging oxygen hole centers, NBOHC), and in situ photoluminescence measurements of NBOHCs to monitor their reactions with ${\mathrm{H}}^{0}$ and ${\mathrm{H}}_{2}$ as a function of time and temperature. A smalle…

PhysicsDiffusionDangling bondQuantum yieldCondensed Matter PhysicsLaserElectronic Optical and Magnetic MaterialsAmorphous solidlaw.inventionNonbridging oxygenCrystallographyDistribution functionlawIrradiationPhysical Review B
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Similar chemical structures, dissimilar triplet quantum yields: a CASPT2 model rationalizing the trend of triplet quantum yields in nitroaromatic sys…

2019

The photophysics of nitroaromatics compounds stand out for being characterized by an ultrafast decay into the triplet manifold and by a significant value of the triplet quantum yield. The latter quantity can change dramatically from one system to another, as proven for the molecules 2- nitronaphthalene, 1-nitronaphthalene, and 2methyl-1nitronaphthale, whose triplet quantum yield have been previously measured to be 0.93 ± 0.15, 0.64 ± 0.12, and 0.33 ± 0.05, respectively (J. Phys. Chem. A 2013, 117, 14100). In the present contribution we rationalize the reported trend for the triplet quantum yield on the basis of the different ability that the excited S 1 state has in the three molecules to r…

PhysicsGeneral Physics and AstronomyQuantum yield02 engineering and technologyConical intersection010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMolecular physics0104 chemical sciencesNitrobenzenechemistry.chemical_compoundchemistryExcited stateMoleculePhysical and Theoretical ChemistryTriplet state0210 nano-technologyGround stateQuantumFisicoquímicaPhysical Chemistry Chemical Physics
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On the Intrinsically Low Quantum Yields of Pyrimidine DNA Photodamages: Evaluating the Reactivity of the Corresponding Minimum Energy Crossing Points

2020

The low quantum yield of photoformation of cyclobutane pyrimidine dimers and pyrimidine-pyrimidone (6-4) adducts in DNA bases is usually associated with the presence of more favorable nonreactive decay paths and with the unlikeliness of exciting the system in a favorable conformation. Here, we prove that the ability of the reactive conical intersection to bring the system either back to the absorbing conformation or to the photoproduct must be considered as a fundamental factor in the low quantum yields of the mentioned photodamage. In support of the proposed model, the one order of magnitude difference in the quantum yield of formation of the cyclobutane thymine dimer with respect to the t…

PyrimidineUltraviolet RaysQuantum yieldPyrimidine dimer010402 general chemistryPhotochemistry01 natural sciencesNucleobaseAdductCyclobutanechemistry.chemical_compound0103 physical sciencesComputer SimulationGeneral Materials SciencePhysical and Theoretical Chemistry010304 chemical physicsChemistryDNAConical intersectionPhotochemical Processes0104 chemical sciences3. Good healthThymineEstructura químicaPyrimidine DimersFisicoquímica
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Determination of the relative quantum yields of the conformational species of autoassociating polypeptide gramicidin A in organic solvent using combi…

1987

Abstract A simple, novel method is proposed for the accurate determination of the relative quantum yields of each of the interconverting conformational species of the autoassociating polypeptide gramicidin A in organic solution. The method is based on fitting the experimental results obtained independently from fluorescence emission spectroscopy and high performance liquid chromatography. The fluorescence parameters obtained are discussed in terms of the structural features of the individual conformational species. The advantages of this approach and its possible application to other different organic solvents or to other autoassociating polypeptides are also considered.

Quantitative Biology::BiomoleculesChromatographyAqueous solutionChemistryComputational chemistryGeneral EngineeringQuantum yieldMoleculeEmission spectrumSolvent effectsFluorescenceHigh-performance liquid chromatographyFluorescence spectroscopySpectrochimica Acta Part A: Molecular Spectroscopy
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Unified model for the ultrafast decay of pyrimidine nucleobases.

2006

Ultrafast decay processes detected after absorption of UV radiation in gas-phase pyrimidine nucleobases uracil, thymine, and cytosine are ascribed to the barrierless character of the pathway along the low-lying 1(pipi*) hypersurface connecting the Franck-Condon region with an out-of-plane distorted ethene-like conical intersection with the ground state. Longer lifetime decays and low quantum yield emission are on the other hand related to the presence of a 1(pipi*) state planar minimum on the S1 surface and the barriers to access other conical intersections. A unified model for the three systems is established on the basis of accurate multiconfigurational CASPT2 calculations, whereas the ef…

Quantitative Biology::BiomoleculesPyrimidineQuantum yieldUracilUnified ModelConical intersectionPyrimidine NucleosidesSurfaces Coatings and FilmsNucleobaseThyminechemistry.chemical_compoundchemistryModels ChemicalMaterials ChemistryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsGround stateThe journal of physical chemistry. B
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Persistent electron-transfer state of a pi-complex of acridinium ion inserted between porphyrin rings of cofacial bisporphyrins

2006

A free-base cofacial bisporphyrin, H(4)DPOx, forms a pi-complex with acridinium ion (AcH(+)) by pi-pi interaction in benzonitrile (PhCN). Formation of the H(4)DPOx-AcH(+) pi-complex was probed by UV-vis and NMR spectroscopy. The binding constant between AcH(+) and H(4)DPOx is determined as 9.7 x 10(4) M(-)(1). Photoinduced electron transfer (ET) from the H(4)DPOx to the AcH(+) moiety occurred efficiently in the pi-complex to form the ET state (H(4)DPOx(*)(+)-AcH(*)). The ET state is successfully detected by laser flash photolysis. The lifetime of the ET state is 18 mus in PhCN at 298 K, and the quantum yield of the ET state is 90%. The temperature dependence of the ET state lifetime has bee…

Quantum yield010402 general chemistryPhotochemistry01 natural sciencesBiochemistryCatalysisPhotoinduced electron transferbisporphyrinchemistry.chemical_compoundElectron transferColloid and Surface Chemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistrypie-complexComputingMilieux_MISCELLANEOUS010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyPorphyrin0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryBenzonitrilechemistry[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryFlash photolysisSteady state (chemistry)
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