Correlation of π-Conjugated Oligomer Structure with Film Morphology and Organic Solar Cell Performance
about
Probing Charge Transfer and Hot Carrier Dynamics in Organic Solar Cells with Terahertz SpectroscopyHydrogen bonding in bulk heterojunction solar cells: a case study.Solution-processed small-molecule solar cells: breaking the 10% power conversion efficiencyOptimization of molecular organization and nanoscale morphology for high performance low bandgap polymer solar cells.Molecular materials for organic photovoltaics: small is beautiful.Oligothiophene wires: impact of torsional conformation on the electronic structure.Impact of mesoscale order on open-circuit voltage in organic solar cells.Solution processable diketopyrrolopyrrole (DPP) cored small molecules with BODIPY end groups as novel donors for organic solar cells.Optimization of solution-processed oligothiophene:fullerene based organic solar cells by using solvent additives.Influence of Molecular Conformations and Microstructure on the Optoelectronic Properties of Conjugated Polymers.Theoretical design of donor-acceptor conjugated copolymers based on furo-, thieno-, and selenopheno[3,4-c] thiophene-4,6-dione and benzodithiophene units for organic solar cells.New conjugated molecules with two and three dithienyldiketopyrrolopyrrole (DPP) moieties substituted at meta positions of benzene toward p- and n-type organic photovoltaic materials.Dithienopyrrole-based oligothiophenes for solution-processed organic solar cells.A potential perylene diimide dimer-based acceptor material for highly efficient solution-processed non-fullerene organic solar cells with 4.03% efficiency.Cyanated isoindigos for n-type and ambipolar organic thin film transistors.Microcavity-embedded, colour-tuneable, transparent organic solar cells.Graphene quantum dots as the hole transport layer material for high-performance organic solar cells.Solution-processed, molecular photovoltaics that exploit hole transfer from non-fullerene, n-type materials.Solvent additive effects on small molecule crystallization in bulk heterojunction solar cells probed during spin casting.π-Bridge modification of thiazole-bridged DPP polymers for high performance near-IR OSCs.Thiophene-Based Organic Semiconductors.Simple and versatile molecular donors for organic photovoltaics prepared by metal-free synthesis.Experimental and theoretical studies of quadrupolar oligothiophene-cored chromophores containing dimesitylboryl moieties as π-accepting end-groups: syntheses, structures, fluorescence, and one- and two-photon absorption.8.4% efficient fullerene-free organic solar cells exploiting long-range exciton energy transfer.Easy Access to NO2 -Containing Donor-Acceptor-Acceptor Electron Donors for High Efficiency Small-Molecule Organic Solar Cells.Real-space visualization of conformation-independent oligothiophene electronic structure.Sequence Effects in Conjugated Donor-Acceptor Trimers and Polymers.The Importance of End Groups for Solution-Processed Small-Molecule Bulk-Heterojunction Photovoltaic Cells.Photon-absorbing charge-bridging states in organic bulk heterojunctions consisting of diketopyrrolopyrrole derivatives and PCBM.Electronic structure and excited state dynamics in a dicyanovinyl-substituted oligothiophene on Au(111).Organic soluble and uniform film forming oligoethylene glycol substituted BODIPY small molecules with improved hole mobility.Stable and easily accessible functional dyes: dihydrotetraazaanthracenes as versatile precursors for higher acenes.Benzochalcogenodiazole-based donor-acceptor-acceptor molecular donors for organic solar cells.Spontaneous formation of light-trapping nano-structures for top-illumination organic solar cells.Theoretical investigations on fluorinated and cyano copolymers for improvements of photovoltaic performances.Influence of Meso and Nanoscale Structure on the Properties of Highly Efficient Small Molecule Solar CellsFused H-shaped tetrathiafulvalene–oligothiophenes as charge transport materials for OFETs and OPVsUnprecedented low energy losses in organic solar cells with high external quantum efficiencies by employing non-fullerene electron acceptorsAcceptor-SubstitutedS,N-Heteropentacenes of Different Conjugation Length: Structure-Property Relationships and Solar Cell PerformanceA-D-A-typeS,N-Heteropentacenes: Next-Generation Molecular Donor Materials for Efficient Vacuum-Processed Organic Solar Cells
P2860
Q33828658-EE26E2E3-5406-4D56-8ED5-AB978369A1E6Q33907041-E8C70577-42EA-4DD5-AF44-5FAA386D63E1Q37347797-89ED499F-CF6E-4191-8882-F396B19EBF76Q38183647-422BB500-5D9B-47C1-8622-7CEDCD94521CQ38200929-129B68D1-7BF6-4727-AE0A-F02CCE180AA1Q40067998-D7BE7D78-0C29-499B-91B5-78B74478A9F3Q41659128-AC7FD8AB-35E6-4BEC-A378-DC856434A4A6Q41847083-1E71B831-F401-499A-B5D1-1DCE68D873CDQ41879106-CA276F04-8F89-4F56-A230-93A36DC8577BQ41895674-929066D7-E9E8-4A8B-8DE3-987F8E58B701Q42611439-48B14736-3986-4C4E-9F12-71A4C56B3551Q42656392-A88CDC70-9E30-423D-89F8-61E54C19F747Q43600952-030ACF7F-F5BA-4CBB-B583-1F9745B3224BQ44572358-8CDA61C3-C478-4FC7-8E49-392CCD5652A7Q45638296-B7942FA1-88E1-4EC7-BFE5-D2D338F0304BQ45746677-A864599D-8270-4AA9-AB9B-80B2A6334113Q46141641-D14BE640-5F08-447E-8663-7CA8EE31D5ADQ46794443-C51E0D47-A977-4CA9-91DC-24A97B8FC815Q46851120-7133F78B-7723-47AE-9615-56000774D35DQ47230161-2BEB58AF-2A3B-4F84-83A1-5F4FD1A98611Q48139251-78AC3DEC-BA4C-4C89-A21B-33C2ACDEDA4AQ50220204-2BA49E8B-D131-4C41-A94A-D2662E2F837CQ51059794-BCC39658-9236-4B02-8837-1A9FFDB877A6Q51104478-EC81D063-24AD-4087-A003-F14E3A2554F3Q51321651-3E1DF89E-724E-4E69-BD70-C64140B0A49AQ51323136-C88B67A0-8599-452B-BEB1-88FAF6CB88B2Q51371028-E6E49764-D1EA-4AED-8EBA-0F2D41D9023EQ51420946-138275E7-0018-49B1-B518-9656E26F329FQ51439638-0130B0CF-C15B-4D93-A570-576CACDF516AQ52862003-A3C51D01-914E-49B3-B156-2FB57067601FQ53539289-260ECEF5-21BA-4C56-8C30-8A2647863454Q53554485-AE9F3F23-C5CA-4BC9-AC97-D5A19AA72541Q53627643-354476BD-C897-4025-83D1-544716830FF6Q53639824-D7A23226-5547-4976-8919-5535783D70AEQ53668617-65B7B1B6-B2D0-4B03-B012-CC8ED6958EDDQ57563090-FD839C33-3F2C-4CC8-B7A5-58CD07F5496BQ57564998-BF1E3939-4D80-410C-A290-843C87D81EABQ57777582-0FDD6200-8589-4987-A6DF-8DA0203F4CB0Q57777600-4D776E08-8E16-41EF-A182-4CDBF7BFC67AQ57777620-94AEBEE4-FD3B-465B-AD56-FF96C3B6BB2E
P2860
Correlation of π-Conjugated Oligomer Structure with Film Morphology and Organic Solar Cell Performance
description
article
@en
im Juni 2012 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 2012
@uk
ലേഖനം
@ml
name
Correlation of π-Conjugated Ol ...... Organic Solar Cell Performance
@en
Correlation of π-Conjugated Ol ...... Organic Solar Cell Performance
@nl
type
label
Correlation of π-Conjugated Ol ...... Organic Solar Cell Performance
@en
Correlation of π-Conjugated Ol ...... Organic Solar Cell Performance
@nl
prefLabel
Correlation of π-Conjugated Ol ...... Organic Solar Cell Performance
@en
Correlation of π-Conjugated Ol ...... Organic Solar Cell Performance
@nl
P2093
P50
P356
P1476
Correlation of π-Conjugated Ol ...... Organic Solar Cell Performance
@en
P2093
Chris Elschner
Christian Körner
Christian Uhrich
Egon Reinold
Elena Mena-Osteritz
Gisela Schulz
Hannah Ziehlke
Martin Pfeiffer
Matthias Weil
Peter Bäuerle
P304
11064-11067
P356
10.1021/JA302320C
P407
P577
2012-06-26T00:00:00Z