Effects of oligothiophene π-bridge length on physical and photovoltaic properties of star-shaped molecules for bulk heterojunction solar cells
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Christoph J. Brabec | Derya Baran | Tayebeh Ameri | M. A. Shcherbina | Yuriy N. Luponosov | Petr V. Dmitryakov | Sergei N. Chvalun | Sergei A. Ponomarenko | Jie Min | Artem V. Bakirov | C. Brabec | S. Chvalun | D. Baran | J. Min | Y. Luponosov | S. Ponomarenko | T. Ameri | S. Peregudova | Svetlana M. Peregudova | A. Bakirov | P. Dmitryakov | Nina Kausch-Busies | Maxim A. Shcherbina | Nina Kausch-Busies | M. Shcherbina | Derya Baran
[1] Christoph J. Brabec,et al. Alkyl Chain Engineering of Solution‐Processable Star‐Shaped Molecules for High‐Performance Organic Solar Cells , 2014 .
[2] Yang Yang,et al. Solution-processed small-molecule solar cells: breaking the 10% power conversion efficiency , 2013, Scientific Reports.
[3] Weiwei Li,et al. Effect of structure on the solubility and photovoltaic properties of bis-diketopyrrolopyrrole molecules , 2013 .
[4] J. Roncali,et al. Tuning of the Photovoltaic Parameters of Molecular Donors by Covalent Bridging , 2013 .
[5] Daoben Zhu,et al. A Solution‐Processable Small Molecule Based on Benzodithiophene and Diketopyrrolopyrrole for High‐Performance Organic Solar Cells , 2013 .
[6] H. Tong,et al. Small molecules based on 2,7-carbazole for efficient solution-processed organic solar cells , 2013 .
[7] Alan J. Heeger,et al. Barium: An Efficient Cathode Layer for Bulk-heterojunction Solar Cells , 2013, Scientific Reports.
[8] Qian Zhang,et al. Solution-processed and high-performance organic solar cells using small molecules with a benzodithiophene unit. , 2013, Journal of the American Chemical Society.
[9] Yongfang Li,et al. Solution-Processable Organic Molecule Photovoltaic Materials with Bithienyl-benzodithiophene Central Unit and Indenedione End Groups , 2013 .
[10] Alan J. Heeger,et al. Intensity dependence of current-voltage characteristics and recombination in high-efficiency solution-processed small-molecule solar cells. , 2013, ACS nano.
[11] C. Brabec,et al. A new two-dimensional oligothiophene end-capped with alkyl cyanoacetate groups for highly efficient solution-processed organic solar cells. , 2013, Chemical communications.
[12] Yongfang Li,et al. Synthesis and photovoltaic properties of a D–A copolymer of dithienosilole and fluorinated-benzotriazole , 2013 .
[13] Hongzheng Chen,et al. Star-shaped D-A small molecules based on diketopyrrolopyrrole and triphenylamine for efficient solution-processed organic solar cells. , 2013, ACS applied materials & interfaces.
[14] Thuc‐Quyen Nguyen,et al. Effects of Heteroatom Substitutions on the Crystal Structure, Film Formation, and Optoelectronic Properties of Diketopyrrolopyrrole‐Based Materials , 2013 .
[15] Christoph J. Brabec,et al. A solution-processable star-shaped molecule for high-performance organic solar cells via alkyl chain engineering and solvent additive , 2013 .
[16] Alan J. Heeger,et al. Narrow-band-gap conjugated chromophores with extended molecular lengths. , 2012, Journal of the American Chemical Society.
[17] Yongfang Li,et al. Conjugated Side-Chain-Isolated D–A Copolymers Based on Benzo[1,2-b:4,5-b′]dithiophene-alt-dithienylbenzotriazole: Synthesis and Photovoltaic Properties , 2012 .
[18] A. Facchetti,et al. A "zig-zag" naphthodithiophene core for increased efficiency in solution-processed small molecule solar cells. , 2012, Chemical communications.
[19] Soo‐Hyoung Lee,et al. Novel naphtho[1,2-b:5,6-b′]dithiophene core linear donor–π–acceptor conjugated small molecules with thiophene-bridged bithiazole acceptor: design, synthesis, and their application in bulk heterojunction organic solar cells , 2012 .
[20] Pei Cheng,et al. Small molecules based on bithiazole for solution-processed organic solar cells , 2012 .
[21] Ignaty Leshchiner,et al. Bithiophenesilane-Based Dendronized Polymers: Facile Synthesis and Properties of Novel Highly Branched Organosilicon Macromolecular Structures , 2012 .
[22] Klaus Meerholz,et al. Efficient solution-processed bulk heterojunction solar cells by antiparallel supramolecular arrangement of dipolar donor-acceptor dyes. , 2011, Angewandte Chemie.
[23] J. Roncali,et al. Unsymmetrical Triphenylamine‐Oligothiophene Hybrid Conjugated Systems as Donor Materials for High‐Voltage Solution‐Processed Organic Solar Cells , 2011 .
[24] Yongfang Li,et al. Solution-Processable Star-Shaped Molecules with Triphenylamine Core and Dicyanovinyl Endgroups for Organic Solar Cells† , 2011 .
[25] Thuc-Quyen Nguyen,et al. Small Molecule Solution-Processed Bulk Heterojunction Solar Cells† , 2011 .
[26] Thuc‐Quyen Nguyen,et al. Influence of alkyl substituents and thermal annealing on the film morphology and performance of solution processed, diketopyrrolopyrrole-based bulk heterojunction solar cells , 2009 .
[27] Thuc-Quyen Nguyen,et al. Nanoscale Phase Separation and High Photovoltaic Efficiency in Solution‐Processed, Small‐Molecule Bulk Heterojunction Solar Cells , 2009 .
[28] Jean Roncali,et al. Molecular bulk heterojunctions: an emerging approach to organic solar cells. , 2009, Accounts of chemical research.
[29] Martin Egginger,et al. Material Solubility‐Photovoltaic Performance Relationship in the Design of Novel Fullerene Derivatives for Bulk Heterojunction Solar Cells , 2009 .
[30] Scaling analysis of the morphology of nanostructured poly(p-xylylene) films synthesized by vapor deposition polymerization , 2008 .
[31] J. Roncali,et al. Light‐Emitting Organic Solar Cells Based on a 3D Conjugated System with Internal Charge Transfer , 2006 .
[32] P. Frère,et al. A star-shaped triphenylamine pi-conjugated system with internal charge-transfer as donor material for hetero-junction solar cells. , 2006, Chemical communications.
[33] Jean Roncali,et al. Triphenylamine-thienylenevinylene hybrid systems with internal charge transfer as donor materials for heterojunction solar cells. , 2006, Journal of the American Chemical Society.
[34] Xiaoniu Yang,et al. Nanoscale morphology of high-performance polymer solar cells. , 2005, Nano letters.
[35] M. Melucci,et al. Solution-phase microwave-assisted synthesis of unsubstituted and modified alpha-quinque- and sexithiophenes. , 2004, The Journal of organic chemistry.
[36] C. Brabec,et al. Origin of the Open Circuit Voltage of Plastic Solar Cells , 2001 .
[37] C. Brabec,et al. Plastic Solar Cells , 2001 .
[38] Toh-Ming Lu,et al. Characterization of Amorphous and Crystalline Rough Surface: Principles and Applications , 2001 .
[39] H. Sun,et al. COMPASS: An ab Initio Force-Field Optimized for Condensed-Phase ApplicationsOverview with Details on Alkane and Benzene Compounds , 1998 .
[40] Paul Meakin,et al. Fractals, scaling, and growth far from equilibrium , 1998 .
[41] Pengyu Y. Ren,et al. The COMPASS force field: parameterization and validation for phosphazenes , 1998 .
[42] Huai Sun,et al. Computer simulations of poly(ethylene oxide): force field, pvt diagram and cyclization behaviour , 1997 .
[43] J. Hummelen,et al. Polymer Photovoltaic Cells: Enhanced Efficiencies via a Network of Internal Donor-Acceptor Heterojunctions , 1995, Science.
[44] N. Kotov,et al. Spreading of Clay Organocomplexes on Aqueous Solutions: Construction of Langmuir-Blodgett Clay Organocomplex Multilayer Films , 1994 .
[45] A. Rappé,et al. Application of a universal force field to metal complexes , 1993 .
[46] A. Rappé,et al. Application of a Universal Force Field to Organic Molecules , 1992 .
[47] W. Goddard,et al. UFF, a full periodic table force field for molecular mechanics and molecular dynamics simulations , 1992 .
[48] G. Cahiez,et al. Organomanganese (II) reagents XXIII: Manganese-catalyzed acylation of organomagnesium compounds by car☐ylic acid chlorides , 1992 .