Search results for "Acceptor"

showing 10 items of 394 documents

Minimizing geminate recombination losses in small-molecule-based organic solar cells

2019

Small-molecule-based organic solar cells (OSCs) are a recurrent alternative to polymer-based OSCs. Due to the higher purity and definition of small molecules compared to polymers, the morphological requirements can be more relaxed. Here, we present a series of novel rhodanine-based small-molecule electron donors and blend them with the standard acceptor PC70BM. By performing a target analysis on femtosecond spectroscopy data, we quantify the rates of geminate charge recombination. We are able to reproduce these rates by applying the Marcus–Levich–Jortner equation, using results from quantum chemical calculations. This shows that in a series of differently substituted compounds, one can corr…

chemistry.chemical_classificationMaterials scienceOrganic solar cellPhotovoltaic systemQuímica orgánicafood and beverages02 engineering and technologyGeneral ChemistryPolymerElectron010402 general chemistry021001 nanoscience & nanotechnology7. Clean energy01 natural sciencesSmall moleculeAcceptor0104 chemical scienceschemistryChemical physicsMaterials ChemistryCyclic voltammetry0210 nano-technologyFemtochemistryJournal of Materials Chemistry C
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Discotic liquid crystals at the air water interface

1991

The monolayer properties of two types of discotic liquid crystals, hexasubstituted triphenylenes 1 and azo derivatives of phloroglucinol 5, were examined. First investigations show that these discotic liquid crystals form stable monolayers. It could be shown that electron acceptors insert into the monolayer of 1. Azo discs display a packing behaviour at the monolayer that is ascribed to a side-on packing of the molecules.

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsAir water interfaceDiscotic liquid crystalOrganic ChemistryElectron acceptorCondensed Matter PhysicsCrystallographychemistryMonolayerMaterials ChemistryOrganic chemistryMoleculeColumnar phaseMakromolekulare Chemie. Macromolecular Symposia
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3,3'-Bicarbazole structural derivatives as charge transporting materials for use in OLED devices

2018

In this study we report novel 3,3′-bicarbazole based charge transporting materials mainly designed for a use in systems containing phosphorescent iridium (III) complex emitters. A low-cost oxidative coupling reaction using FeCl3 was employed in the synthesis of 3,3′-bicarbazole compounds. Different derivatives of 3,3′-bicarbazole with 4-ethoxyphenyland ethyl- substituents at 9,9′- positions and (2,2-diphenylhydrazono)methyl- and 4-(dimethylamino)styryl- substituents at 6,6′- positions were synthesized. Obtained (2,2-diphenylhydrazono)methyl- derivatives exhibit glass transition temperatures that are sufficient for applications in electronic devices. Thin amorphous films of good optical qual…

chemistry.chemical_classificationMaterials sciencechemistryElectron affinityOLEDPhysical chemistrychemistry.chemical_elementMoleculeIridiumElectron acceptorGlass transitionPhosphorescenceAmorphous solidOrganic Electronics and Photonics: Fundamentals and Devices
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The First sulfur-containing twin-DCNQI-type acceptor

1994

chemistry.chemical_classificationMechanics of MaterialsChemistryMechanical EngineeringPolymer chemistryOrganic chemistryGeneral Materials ScienceElectronic structureElectron acceptorSulfur containingAcceptorChemical synthesisAdvanced Materials
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The Quest for Mononuclear Gold(II) and Its Potential Role in Photocatalysis and Drug Action.

2017

The chemistry of gold strongly focuses on the ubiquitous oxidation states +I and +III. The intermediate oxidation state +II is generally avoided in mononuclear gold species. In recent years, gold(II) has been increasingly suggested as a key intermediate in artificial photosynthesis systems, with gold(III) moieties acting as electron acceptors, as well as in gold-catalyzed photoredox catalysis and radical chemistry. This Minireview provides a concise summary of confirmed and characterized mononuclear open-shell gold(II) complexes. Recent findings on structural motifs and reactivity patterns will be discussed. Exciting developments in the fields of photosynthesis, photocatalysis, and potentia…

chemistry.chemical_classificationMolecular Structure010405 organic chemistryChemistryRadicalChemistry PharmaceuticalPhotoredox catalysisElectronsGeneral ChemistryElectron acceptor010402 general chemistryPhotochemical Processes01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesArtificial photosynthesisElectron transferOxidation statePhotocatalysisOrganic chemistryReactivity (chemistry)Organogold CompoundsAngewandte Chemie (International ed. in English)
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Novel dithieno[3,2-b:2′,3′-d]pyrrole-based organic dyes with high molar extinction coefficient for dye-sensitized solar cells

2013

Abstract Three new metal-free organic dyes FD1 – 3 with a planar dithieno[3,2- b :2′,3′- d ]pyrrole unit as linker were synthesized and used for dye-sensitized solar cells with high molar extinction coefficients. In this work, dithieno[3,2- b :2′,3′- d ]pyrrole was employed as π-conjugated bridge to construct A–π– d –π–A organic dyes, where 9,9-dihexyl-9 H -fluorene was used as a donor, and cyanoacrylic acid as an electron acceptor. For a typical device, a solar energy conversion efficiency ( η ) of 6.36% based on FD2 was achieved under simulated AM 1.5 solar irradiation (100 mW cm −2 ) with a short-circuit photocurrent density ( J sc ) of 13.76 mA cm −2 , an open-circuit voltage ( V oc ) o…

chemistry.chemical_classificationPhotocurrentMaterials scienceGeneral ChemistryElectron acceptorMolar absorptivityFluoreneCondensed Matter PhysicsPhotochemistryElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundDye-sensitized solar cellchemistryExtinction (optical mineralogy)Materials ChemistryIrradiationElectrical and Electronic EngineeringPyrroleOrganic Electronics
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Solution processable 2-(trityloxy)ethyl and tert-butyl group containing amorphous molecular glasses of pyranylidene derivatives with light-emitting a…

2015

Abstract Small organic molecules with incorporated 4 H -pyran-4-ylidene (pyranylidene) fragment as the π-conjugation system which bonds the electron acceptor fragment (A) with electron donor part (D) in the molecule – also well known as derivatives of 4-(dicyano-methylene)-2-methyl-6-[p-(dimethylamino)styryl]-4H-pyran ( DCM ) laser dye-have attracted considerable attention of scientists as potential new generation materials for organic photonics and molecular electronics due to their low-cost fabrication possibility, flexibility and low-weight. Six glassy derivatives of 4 H -pyran-4-ylidene (pyranylidene) with attached bulky 2-(trityloxy)ethyl and tert -butyl groups are described in this re…

chemistry.chemical_classificationPhotoluminescenceMaterials scienceOrganic ChemistryElectroluminescenceElectron acceptorPhotochemistryAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsAmorphous solidInorganic ChemistrychemistryMoleculeLight emissionElectrical and Electronic EngineeringPhysical and Theoretical ChemistryGlass transitionHOMO/LUMOSpectroscopyOptical Materials
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1998

Reaction centers (RC) from the species Erythrobacter (Eb.) litoralis, Erythromonas (Em.) ursincola and Sandaracinobacter (S.) sibiricus have been purified by LDAO treatment of light-harvesting-reaction center complexes and DEAE chromatography. The content and overall organisation of the RCs' chromophores, determined by linear dichroism (LD) and absorption spectroscopy, are similar to those isolated from anaerobic photosynthetic bacteria. The redox properties of the primary electron donor are pH-independent and very similar to those determined for anaerobic photosynthetic bacteria with midpoint potential values equal to 445 (± 10), 475 and 510 mV for Eb. litoralis, S. sibiricus and Em. ursin…

chemistry.chemical_classificationPhotosynthetic reaction centreErythrobacter litoralisCytochromebiologyAerobic bacteriaStereochemistryCell BiologyPlant ScienceGeneral MedicineElectron acceptorbiology.organism_classificationPhotosynthesisBiochemistryMicrobiologychemistrybiology.proteinPhotosynthetic bacteriaBacteriaPhotosynthesis Research
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ChemInform Abstract: Oppenauer Oxidation of Secondary Alcohols with 1,1,1-Trifluoroacetone as Hydride Acceptor.

2008

1,1,1-Trifluoroacetone (2a) reacts as a hydride-acceptor in the Oppenauer oxidation of secondary alcohols (1) in the presence of diethylethoxyaluminum. The oxidant allows for selective oxidation of secondary alcohols in the presence of primary alcohols.

chemistry.chemical_classificationPrimary (chemistry)HydrideChemistryOppenauer oxidationGeneral MedicineBridged compoundsMedicinal chemistryAcceptorChemInform
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Phenothiazine-based dyes with bilateral extension of π-conjugation for efficient dye-sensitized solar cells

2013

Four novel organic photo-sensitizers based on phenothiazine were designed, synthesized and characterized for efficient dye-sensitized solar cells. Anisole, octyloxybenzene and dodecyloxybenzene were incorporated into the phenothiazine by an Ullmann reaction. An additional octyloxybenzene was incorporated into one dye unit through a Suzuki coupling reaction. The modified phenothiazine moiety acts as an electron donor and cyanoacrylic acid acts as an electron acceptor and anchoring unit. The photophysical, electrochemical and sensitizing characteristics of the new dyes were evaluated. The bis(octyloxybenzene) substituted dye delivered the best performance with its sensitized solar cell displa…

chemistry.chemical_classificationProcess Chemistry and TechnologyGeneral Chemical EngineeringElectron donorElectron acceptorPhotochemistryUllmann reactionlaw.inventionchemistry.chemical_compoundDye-sensitized solar cellSuzuki reactionchemistrylawPhenothiazineSolar cellMoietyDyes and Pigments
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