WITHDRAWN: Cosensitization process effect of D-A-π-A featured dyes on photovoltaic performances☆

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[1]  M. Grätzel,et al.  Unravel the Impact of Anchoring Groups on the Photovoltaic Performances of Diketopyrrolopyrrole Sensitizers for Dye-Sensitized Solar Cells , 2015 .

[2]  Junxiang Zhang,et al.  Effect of Molecular Structure Perturbations on the Performance of the D–A−π–A Dye Sensitized Solar Cells , 2014 .

[3]  Effect of a long alkyl group on cyclopentadithiophene as a conjugated bridge for D-A-π-A organic sensitizers: IPCE, electron diffusion length, and charge recombination. , 2014, ACS applied materials & interfaces.

[4]  Kenji Kakiage,et al.  Fabrication of a high-performance dye-sensitized solar cell with 12.8% conversion efficiency using organic silyl-anchor dyes. , 2015, Chemical communications.

[5]  M. Grätzel,et al.  A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films , 1991, Nature.

[6]  Xin Li,et al.  Organic D‐A‐π‐A Solar Cell Sensitizers with Improved Stability and Spectral Response , 2011 .

[7]  H. Tian,et al.  Rational molecular engineering of cyclopentadithiophene-bridged D-A-π-A sensitizers combining high photovoltaic efficiency with rapid dye adsorption , 2015, Scientific Reports.

[8]  Y. Eom,et al.  Thieno[3,2‐b][1]benzothiophene Derivative as a New π‐Bridge Unit in D–π–A Structural Organic Sensitizers with Over 10.47% Efficiency for Dye‐Sensitized Solar Cells , 2015 .

[9]  T. Lan,et al.  A near-infrared dithieno[2,3-a:3',2'-c]phenazine-based organic co-sensitizer for highly efficient and stable quasi-solid-state dye-sensitized solar cells. , 2014, ACS applied materials & interfaces.

[10]  Zhen Li,et al.  New triphenylamine-based sensitizers bearing double anchor units for dye-sensitized solar cells , 2015, Science China Chemistry.

[11]  Liyuan Han,et al.  Improvement of efficiency of dye-sensitized solar cells based on analysis of equivalent circuit , 2006 .

[12]  Zhihui Wang,et al.  Significant Enhancement of Open-Circuit Voltage in Indoline-Based Dye-Sensitized Solar Cells via Retarding Charge Recombination , 2013 .

[13]  N-Annulated perylene-based metal-free organic sensitizers for dye-sensitized solar cells. , 2015, Chemical communications.

[14]  Ping Chen,et al.  Lending Triarylphosphine Oxide to Phenanthroline: a Facile Approach to High‐Performance Organic Small‐Molecule Cathode Interfacial Material for Organic Photovoltaics utilizing Air‐Stable Cathodes , 2014 .

[15]  P. Liska,et al.  Engineering of efficient panchromatic sensitizers for nanocrystalline TiO(2)-based solar cells. , 2001, Journal of the American Chemical Society.

[16]  O. Inganäs,et al.  D-A(1)-D-A(2) Copolymers with Extended Donor Segments for Efficient Polymer Solar Cells , 2015 .

[17]  Effects of various π-conjugated spacers in thiadiazole[3,4-c]pyridine-cored panchromatic organic dyes for dye-sensitized solar cells , 2015 .

[18]  M. Liang,et al.  Influence of the Terminal Electron Donor in D-D-π-A Organic Dye-Sensitized Solar Cells: Dithieno[3,2-b:2',3'-d]pyrrole versus Bis(amine). , 2015, ACS applied materials & interfaces.

[19]  Yu-Cheng Chang,et al.  Highly efficient porphyrin-sensitized solar cells with enhanced light harvesting ability beyond 800 nm and efficiency exceeding 10% , 2014 .

[20]  Basile F. E. Curchod,et al.  Dye-sensitized solar cells with 13% efficiency achieved through the molecular engineering of porphyrin sensitizers. , 2014, Nature chemistry.

[21]  Shruti A. Agarkar,et al.  Functionally Engineered Egg Albumen Gel for Quasi-Solid Dye Sensitized Solar Cells , 2014 .

[22]  Jiann T. Lin,et al.  2H-[1,2,3]Triazolo[4,5-c]pyridine Cored Organic Dyes Achieving a High Efficiency: a Systematic Study of the Effect of Different Donors and π Spacers. , 2015, ACS applied materials & interfaces.

[23]  Kenji Kakiage,et al.  Highly-efficient dye-sensitized solar cells with collaborative sensitization by silyl-anchor and carboxy-anchor dyes. , 2015, Chemical communications.

[24]  Y. Chang,et al.  Effect of the co-sensitization sequence on the performance of dye-sensitized solar cells with porphyrin and organic dyes. , 2016, Physical chemistry chemical physics : PCCP.

[25]  Yu-Cheng Chang,et al.  A strategy to design highly efficient porphyrin sensitizers for dye-sensitized solar cells. , 2011, Chemical communications.

[26]  S. Zakeeruddin,et al.  Molecular engineering of push-pull porphyrin dyes for highly efficient dye-sensitized solar cells: the role of benzene spacers. , 2014, Angewandte Chemie.

[27]  H. Tian,et al.  Efficient solar cells sensitized by porphyrins with an extended conjugation framework and a carbazole donor: from molecular design to cosensitization. , 2014, Angewandte Chemie.

[28]  P. Chou,et al.  Highly efficient dye-sensitized solar cells based on panchromatic ruthenium sensitizers with quinolinylbipyridine anchors. , 2014, Angewandte Chemie.

[29]  G. Gigli,et al.  Sustainability of Organic Dye-Sensitized Solar Cells: The Role of Chemical Synthesis , 2015 .

[30]  G. Boschloo,et al.  Carbazole‐Based Hole‐Transport Materials for Efficient Solid‐State Dye‐Sensitized Solar Cells and Perovskite Solar Cells , 2014, Advanced materials.

[31]  H. Tian,et al.  Cosensitization of D-A-π-A quinoxaline organic dye: efficiently filling the absorption valley with high photovoltaic efficiency. , 2015, ACS applied materials & interfaces.

[32]  H. Tian,et al.  New D-A-π-A organic sensitizers for efficient dye-sensitized solar cells. , 2015, Chemical communications.

[33]  Chulwoo Kim,et al.  Enhancing the Performance of Organic Dye-Sensitized Solar Cells via a Slight Structure Modification , 2011 .

[34]  E. Palomares,et al.  A single atom change “switches-on” the solar-to-energy conversion efficiency of Zn-porphyrin based dye sensitized solar cells to 10.5% , 2015 .

[35]  H. Miura,et al.  Improvement of Light Harvesting by Addition of a Long-Wavelength Absorber in Dye-Sensitized Solar Cells Based on ZnO and Indoline Dyes , 2015 .

[36]  Ping Liu,et al.  Manipulation of the band gap and efficiency of a minimalist push–pull molecular donor for organic solar cells , 2015 .

[37]  A. J. Frank,et al.  Influence of Electrical Potential Distribution, Charge Transport, and Recombination on the Photopotential and Photocurrent Conversion Efficiency of Dye-Sensitized Nanocrystalline TiO2 Solar Cells: A Study by Electrical Impedance and Optical Modulation Techniques , 2000 .

[38]  S. Singh,et al.  Panchromatic Ru (II) Dipyrrins as NCS Free Sensitizers Showing Highest Efficiency for DSSCs , 2015 .

[39]  Michael Grätzel,et al.  Porphyrin-Sensitized Solar Cells with Cobalt (II/III)–Based Redox Electrolyte Exceed 12 Percent Efficiency , 2011, Science.

[40]  H. Tian,et al.  Porphyrin cosensitization for a photovoltaic efficiency of 11.5%: a record for non-ruthenium solar cells based on iodine electrolyte. , 2015, Journal of the American Chemical Society.

[41]  H. Ågren,et al.  Cosensitizers for simultaneous filling up of both absorption valleys of porphyrins: a novel approach for developing efficient panchromatic dye-sensitized solar cells. , 2014, Chemical communications.

[42]  Peng Wang,et al.  A metal-free N-annulated thienocyclopentaperylene dye: power conversion efficiency of 12% for dye-sensitized solar cells. , 2015, Angewandte Chemie.

[43]  Weihong Zhu,et al.  Organic sensitizers from D-π-A to D-A-π-A: effect of the internal electron-withdrawing units on molecular absorption, energy levels and photovoltaic performances. , 2013, Chemical Society reviews.

[44]  Liyuan Han,et al.  Molecular Engineering of New Thienyl‐Bodipy Dyes for Highly Efficient Panchromatic Sensitized Solar Cells , 2014 .

[45]  Licheng Sun,et al.  Phenoxazine-based panchromatic organic sensitizers for dye-sensitized solar cells , 2015 .

[46]  F. D’Souza,et al.  Electron Transfer Studies of High Potential Zinc Porphyrin–Fullerene Supramolecular Dyads , 2014 .

[47]  Weihong Zhu,et al.  Insight into D-A-π-A Structured Sensitizers: A Promising Route to Highly Efficient and Stable Dye-Sensitized Solar Cells. , 2015, ACS applied materials & interfaces.

[48]  H. Tian,et al.  D-A-π-A featured sensitizers bearing phthalimide and benzotriazole as auxiliary acceptor: effect on absorption and charge recombination dynamics in dye-sensitized solar cells. , 2012, ACS applied materials & interfaces.

[49]  P. Chou,et al.  Panchromatic Ru(II) sensitizers bearing single thiocyanate for high efficiency dye sensitized solar cells , 2014 .