다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기
Organic electronics, v.49, 2017년, pp.142 - 151
Lombeck, Florian (Optoelectronics Group, Cavendish Laboratory, J.J. Thomson Avenue, University of Cambridge, Cambridge, CB3 0HE, United Kingdom) , Müllers, Stefan (Makromolekulare Chemie, Universitä) , Komber, Hartmut (t Freiburg, Stefan-Meier-Straße 31, 79104, Freiburg, Germany) , Menke, S. Matthew (Leibniz-Institut fü) , Pearson, Andrew J. (r Polymerforschung Dresden e.V., Hohe Straße 6, 01069, Dresden, Germany) , Conaghan, Patrick J. (Optoelectronics Group, Cavendish Laboratory, J.J. Thomson Avenue, University of Cambridge, Cambridge, CB3 0HE, United Kingdom) , McNeill, Christopher R. (Optoelectronics Group, Cavendish Laboratory, J.J. Thomson Avenue, University of Cambridge, Cambridge, CB3 0HE, United Kingdom) , Friend, Richard H. (Optoelectronics Group, Cavendish Laboratory, J.J. Thomson Avenue, University of Cambridge, Cambridge, CB3 0HE, United Kingdom) , Sommer, Michael (Department of Materials Science and Engineering, Monash University, Wellington Road, Clayton, Victoria, 3800, Australia)
AI-Helper
Abstract The synthesis, characterization and solar cell performance of PCDTBT and its highly soluble analogue hexyl-PCDTBT with cross-conjugated benzoyl moieties at the carbazole comonomer are presented. Through the use of both model reactions and time-controlled microwave-assisted Suzuki polyconde...
Chem. Soc. Rev. Mazzio 44 78 2014 10.1039/C4CS00227J The future of organic photovoltaics
Chem. Soc. Rev. Heeger 39 2354 2010 10.1039/b914956m Semiconducting polymers: the third generation
Chem. Mater. Mei 26 604 2014 10.1021/cm4020805 Side chain engineering in solution-processable conjugated polymers
Sci. China Chem. Zhang 58 192 2015 10.1007/s11426-014-5260-2 Side-chain engineering of high-efficiency conjugated polymer photovoltaic materials
Chem. Rev. Lu 115 12666 2015 10.1021/acs.chemrev.5b00098 Recent advances in bulk heterojunction polymer solar cells
Adv. Mater. Blouin 19 2295 2007 10.1002/adma.200602496 A low-bandgap poly(2,7-carbazole) derivative for use in high-performance solar cells
Adv. Energy Mater. Peters 1 491 2011 10.1002/aenm.201100138 High efficiency polymer solar cells with long operating lifetimes
Adv. Energy Mater. Lombeck 21 1601232 2016 10.1002/aenm.201601232 Organic solar cells: on the effect of prevalent carbazole homocoupling defects on the photovoltaic performance of PCDTBT: PC71BM solar cells
Macrolecules Zotti 35 2122 2002 10.1021/ma011311c Electrochemical, conductive, and magnetic properties of 2,7-carbazole-based conjugated polymers
Chem. Mater. Le 19 2128 2007 10.1021/cm070063h Synthesis and thermoelectric properties of polycarbazole, polyindolocarbazole, and polydiindolocarbazole derivatives
J. Mater. Chem. Manceau 21 4132 2011 10.1039/c0jm03105d Photochemical stability of π-conjugated polymers for polymer solar cells: a rule of thumb
Adv. Energy Mater. Tournebize 4 1 2014 10.1002/aenm.201301530 How photoinduced crosslinking under operating conditions can reduce PCDTBT-based solar cell efficiency and then stabilize it
Nat. Commun. Kong 5 5688 2014 10.1038/ncomms6688 Long-term stable polymer solar cells with significantly reduced burn-in loss
Acc. Chem. Res. Blouin 41 1110 2008 10.1021/ar800057k Poly(2,7-Carbazole)s: structure - property relationships
Macromol. Rapid Commun. Lombeck 36 231 2015 10.1002/marc.201400437 Simple Synthesis of P (Cbz- Alt -TBT ) and PCDTBT by combining direct arylation with Suzuki polycondensation of heteroaryl chlorides
ACS Macro Lett. Lombeck 3 819 2014 10.1021/mz5004147 Identifying homocouplings as critical side reactions in direct arylation polycondensation
Macromolecules Lombeck 49 9382 2016 10.1021/acs.macromol.6b02216 PCDTBT: from polymer photovoltaics to light-emitting diodes by side-chain-controlled luminescence
J. Organom. Chem. Suzuki 576 147 1999 10.1016/S0022-328X(98)01055-9 Recent advances in the cross-coupling reactions of organoboron derivatives with organic electrophiles
Polym. Chem. Metzler 6 3694 2015 10.1039/C5PY00141B High molecular weight mechanochromic spiropyran main chain copolymers via reproducible microwave-assisted Suzuki polycondensation
Macromolecules Kim 44 1909 2011 10.1021/ma102467w Carbazole-based copolymers: effects of conjugation breaks and steric hindrance
Phys. Rev. B - Condens. Matter Mater. Phys. Vandewal 81 1 2010 10.1103/PhysRevB.81.125204 Relating the open-circuit voltage to interface molecular properties of donor:acceptor bulk heterojunction solar cells
Org. Electron. Phys. Mater. Appl. Ratcliff 3 744 2012 Energy level alignment in PCDTBT: PC70BM solar cells: solution processed NiOX for improved hole collection and efficiency
Nat. Photonics Park 3 297 2009 10.1038/nphoton.2009.69 Bulk heterojunction solar cells with internal quantum efficiency approaching 100%
Adv. Energy Mater. Moon 2 304 2012 10.1002/aenm.201100667 Nanomorphology of PCDTBT: PC70BM bulk heterojunction solar cells
Adv. Mater. Liu 24 669 2012 10.1002/adma.201103097 Solvent additive control of morphology and crystallization in semiconducting polymer blends
Angew. Chem. - Int. Ed. Wang 50 5519 2011 10.1002/anie.201101021 Enhancement of donor - acceptor polymer bulk heterojunction solar cell power conversion efficiencies by addition of Au nanoparticles
Appl. Phys. Lett. Chu 95 63304 2009 10.1063/1.3182797 Highly efficient polycarbazole-based organic photovoltaic devices
Angew. Chem. - Int. Ed. Wang 52 2874 2013 10.1002/anie.201209999 Transferable graphene oxide by stamping nanotechnology: electron-transport layer for efficient bulk-heterojunction solar cells
Adv. Energy Mater. Burke 5 1500123 2015 10.1002/aenm.201500123 Beyond Langevin recombination: how equilibrium between free carriers and charge transfer states determines the open-circuit voltage of organic solar cells
J. Am. Chem. Soc. Wang 136 12576 2014 10.1021/ja506785w High open circuit voltage in regioregular narrow band-gap polymer solar cells
J. Am. Chem. Soc. Graham 136 9608 2014 10.1021/ja502985g Importance of the donor:fullerene intermolecular arrangement for high-efficiency organic photovoltaics
J. Mater. Chem. Yi 21 13649 2011 10.1039/c1jm12089a Carbazole and thienyl benzo[1,2,5]thiadiazole based polymers with improved open circuit voltages and processability for application in solar cells
Macrolecules Casey 47 2279 2014 10.1021/ma5000943 Thioalkyl-substituted benzothiadiazole acceptors: copolymerization with carbazole affords polymers with large Stokes shifts and high solar cell voltages
ACS Appl. Mater. Interfaces Kim 6 7523 2014 10.1021/am500891z Synthesis of PCDTBT-based fluorinated polymers for high open-circuit voltage in organic photovoltaics: towards an understanding of relationships between polymer energy levels engineering and ideal morphology control
Nat. Commun. Lu 3 795 2012 10.1038/ncomms1790 Bilayer order in a polycarbazole-conjugated polymer
Adv. Energy Mater. Jung 4 1400432 2014 10.1002/aenm.201400432 All-inkjet-printed, all-air-processed solar cells
Sci. Rep. Kingsley 4 5286 2014 10.1038/srep05286 Molecular weight dependent vertical composition profiles of PCDTBT: PC71BM blends for organic photovoltaics
*원문 PDF 파일 및 링크정보가 존재하지 않을 경우 KISTI DDS 시스템에서 제공하는 원문복사서비스를 사용할 수 있습니다.
저자가 APC(Article Processing Charge)를 지불한 논문에 한하여 자유로운 이용이 가능한, hybrid 저널에 출판된 논문
Copyright KISTI. All Rights Reserved.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.