Donor–Acceptor Conjugated Polymer Based on Naphtho[1,2-c:5,6-c]bis[1,2,5]thiadiazole for High-Performance Polymer Solar Cells
about
Ultrathin polyaniline-based buffer layer for highly efficient polymer solar cells with wide applicabilityEffective D-A-D type chromophore of fumaronitrile-core and terminal alkylated bithiophene for solution-processed small molecule organic solar cellsHighly Efficient and Stable Solar Cells Based on Thiazolothiazole and Naphthobisthiadiazole Copolymers.Solution-processed small-molecule solar cells: breaking the 10% power conversion efficiencyBenzo[1,2-b:4,5-b']dithiophene building block for the synthesis of semiconducting polymers.Organic photoresponse materials and devices.25th anniversary article: isoindigo-based polymers and small molecules for bulk heterojunction solar cells and field effect transistors.Water/alcohol soluble conjugated polymers for the interface engineering of highly efficient polymer light-emitting diodes and polymer solar cells.Low bandgap semiconducting polymers for polymeric photovoltaics.Recent Advances in Wide-Bandgap Photovoltaic Polymers.Surface Structure Modification of ZnO and the Impact on Electronic Properties.Naphthobischalcogenadiazole Conjugated Polymers: Emerging Materials for Organic Electronics.Synthesis of poly(benzothiadiazole-co-dithienobenzodithiophenes) and effect of thiophene insertion for high-performance polymer solar cells.Thiophene-thiazolothiazole copolymers: significant impact of side chain composition on backbone orientation and solar cell performances.A material combination principle for highly efficient polymer solar cells investigated by mesoscopic phase heterogeneity.Synergistic effect of fluorination on molecular energy level modulation in highly efficient photovoltaic polymers.D-π-A-π-A Strategy to Design Benzothiadiazole-carbazole-based Conjugated Polymer with High Solar Cell Voltage and Enhanced Photocurrent.Tuning the electronic and optical properties of NDT-based conjugated polymers by adopting fused heterocycles as acceptor units: a theoretical study.Chiral triptycene-pyrene π-conjugated chromophores with circularly polarized luminescence.A Novel Naphtho[1,2-c:5,6-c']Bis([1,2,5]Thiadiazole)-Based Narrow-Bandgap π-Conjugated Polymer with Power Conversion Efficiency Over 10.Dithienobenzothiadiazole-based conjugated polymer: processing solvent-relied interchain aggregation and device performances in field-effect transistors and polymer solar cells.High polymer/fullerene ratio realized in efficient polymer solar cells by tailoring of the polymer side-chains.Synthesis, optical and electrochemical properties of the A-π-D-π-A porphyrin and its application as an electron donor in efficient solution processed bulk heterojunction solar cells.A roundabout approach to control morphological orientation and solar-cell performance by modulating side-chain branching position in benzodithiophene-based polymers.The synthesis of 5-alkyl[3,4-c]thienopyrrole-4,6-dione-based polymers using a Pd-catalyzed oxidative C-H/C-H homopolymerization reaction.Donor-acceptor-type copolymers based on a naphtho[1,2-c:5,6-c]bis(1,2,5-thiadiazole) scaffold for high-efficiency polymer solar cells.Wide-Bandgap Benzodithiophene-Benzothiadiazole Copolymers for Highly Efficient Multijunction Polymer Solar Cells.Recent advances in polymer solar cells: realization of high device performance by incorporating water/alcohol-soluble conjugated polymers as electrode buffer layer.An easy and effective method to modulate molecular energy level of the polymer based on benzodithiophene for the application in polymer solar cells.Strategies for controlling the active layer morphologies in OPVsDomain Purity, Miscibility, and Molecular Orientation at Donor/Acceptor Interfaces in High Performance Organic Solar Cells: Paths to Further ImprovementCompetition between morphological attributes in the thermal annealing and additive processing of polymer solar cellsLocation, Location, Location - Strategic Positioning of 2,1,3-Benzothiadiazole Units within Trigonal Quaterfluorene-Truxene Star-Shaped StructuresBODIPY-based conjugated polymers for broadband light sensing and harvesting applicationsOptical and electrical properties of dithienothiophene based conjugated polymers: medium donor vs. weak, medium, and strong acceptorsSynthesis and characterization of thieno[3,2-b]thiophene-isoindigo-based copolymers as electron donor and hole transport materials for bulk-heterojunction polymer solar cellsSynthesis of a Novel Low-Bandgap Polymer Based on a Ladder-Type Heptacyclic Arene Consisting of Outer Thieno[3,2-b]thiophene Units for Efficient Photovoltaic ApplicationTrifluoromethylated thieno[3,4-b]thiophene-2-ethyl carboxylate as a building block for conjugated polymersOrganometallic Approaches to Conjugated Polymers for Plastic Solar Cells: From Laboratory Synthesis to Industrial ProductionSynthesis and characterization of benzodithiophene–isoindigo polymers for solar cells
P2860
Q34317962-AF0DCD80-375C-40A5-8368-97BC5D999BF3Q35728008-EF1D1D2C-A424-461D-AE95-B2F7055AD5FBQ36099526-4A1C80EE-F54B-4A0E-B2BF-A6E0B0B470B4Q37347797-7C450AD5-55FD-4485-9309-BD6A77B1A3B3Q37965443-7AE3E0C1-7A4E-430B-865B-F9ACB9C49317Q37967147-29B9FA99-A2A6-43DF-8174-A626395A87EDQ38187629-3DCE0665-B30C-4EBC-9393-F30C9088E561Q38343646-3F0E997B-6258-44C2-AF59-564133C31D5DQ38628025-88864EB4-C4A6-4DB5-84D8-326CC2E0CA96Q38735954-FCD4C19B-BF6B-4804-A180-495310CE47C2Q38758504-F1336013-3B9E-4D9C-91BC-ED045FA2141CQ39152638-C0C11457-811E-4234-A41D-C2060047055AQ43845752-C7328C5A-0F8D-4293-AD20-39311ACCAC56Q44713395-900EBBE9-A199-4B84-A048-4ECEC6EFD924Q45125366-7DACD56F-4F84-45E1-9732-8378C1C292CBQ45399898-285F2F81-C41B-4246-BA13-3A25866BE213Q47605774-9AE477C1-F7F9-4A6A-A2AD-1B83319B81EAQ47921539-2DFE7608-A208-447D-95E3-036B0AC4ECCAQ49791073-84C513C0-9CF3-4911-8E7A-90F627BCBE8CQ51158963-2B6737B9-1D43-4CB9-9FDB-38242DCBEC51Q52780234-80A89E86-4632-4FBF-84BF-F5F718589F5FQ53291062-78F1825E-D846-4BE9-9821-743110FE236AQ53389541-D353C337-33C2-424E-92A8-1B9657BD9B00Q53407536-2A1D1D4A-E1DA-49FB-8ACC-60C2FE5C02F6Q53455834-DF4E49D3-29D8-4321-B968-0D3557CEF404Q53572847-E4922FBA-35C0-4586-808E-C89786691AE4Q53635278-63F59649-9800-4A1E-9662-C39F33C248E9Q53655113-40F91547-FAAD-4090-8053-102ABF6630F3Q54426721-AC5C4E7D-FEA6-466F-889D-18CB2DCC2495Q57379570-213BF530-E3C5-4948-85A1-18AFF246D01CQ57426368-AC1BC943-9108-4469-A9F0-C8AAB4617E3EQ57428828-B86F72E7-DBEC-450C-8A64-43FBCFC5624AQ57565028-C6733C70-6072-4E07-8068-C8A1EBAC0197Q57565066-E8826AE4-AAC1-4841-BDD0-EAAAC8A089B4Q57566945-341A167C-D495-4BB2-A783-3CB93EBD2022Q57637788-29C3ED78-263C-4AB6-8BA7-8A14A4D784ADQ57637789-DBD4B8AE-2FBD-4762-8758-0D33A5A5B5B5Q57688321-C4872AE6-F42E-4AEC-AF51-0ED6586EE4B9Q57718449-B456E021-98CE-4460-862F-9213D11C29DCQ57798357-A88B5D82-C38C-4EF7-A9DA-069141DE902A
P2860
Donor–Acceptor Conjugated Polymer Based on Naphtho[1,2-c:5,6-c]bis[1,2,5]thiadiazole for High-Performance Polymer Solar Cells
description
im Juni 2011 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 06 June 2011
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в червні 2011
@uk
name
Donor–Acceptor Conjugated Poly ...... erformance Polymer Solar Cells
@en
Donor–Acceptor Conjugated Poly ...... erformance Polymer Solar Cells
@nl
type
label
Donor–Acceptor Conjugated Poly ...... erformance Polymer Solar Cells
@en
Donor–Acceptor Conjugated Poly ...... erformance Polymer Solar Cells
@nl
prefLabel
Donor–Acceptor Conjugated Poly ...... erformance Polymer Solar Cells
@en
Donor–Acceptor Conjugated Poly ...... erformance Polymer Solar Cells
@nl
P2093
P356
P1476
Donor-acceptor conjugated poly ...... erformance polymer solar cells
@en
P2093
P304
P356
10.1021/JA201131H
P407
P577
2011-06-06T00:00:00Z