Tailoring of Energy Levels in D-π-A Organic Dyes via Fluorination of Acceptor Units for Efficient Dye-Sensitized Solar Cells
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Jin Young Kim | M. Ko | Honggon Kim | Kyungkon Kim | Doh-Kwon Lee | Jae‐Yup Kim | H. Son | M. Lee | Duckhwan Lee | B. Kim | Jae-Yup Kim
[1] Mohammad Khaja Nazeeruddin,et al. Perovskite as light harvester: a game changer in photovoltaics. , 2014, Angewandte Chemie.
[2] Basile F. E. Curchod,et al. Dye-sensitized solar cells with 13% efficiency achieved through the molecular engineering of porphyrin sensitizers. , 2014, Nature chemistry.
[3] Mohammad Khaja Nazeeruddin,et al. Metal free sensitizer and catalyst for dye sensitized solar cells , 2013 .
[4] Bong-Gi Kim,et al. Molecular design principle of all-organic dyes for dye-sensitized solar cells. , 2013, Chemistry.
[5] Organic Sensitizers with Bridged Triphenylamine Donor Units for Efficient Dye‐Sensitized Solar Cells , 2013 .
[6] Jin Young Kim,et al. Importance of 4-tert-Butylpyridine in Electrolyte for Dye-Sensitized Solar Cells Employing SnO2 Electrode , 2012 .
[7] Ashraful Islam,et al. Aggregation-free branch-type organic dye with a twisted molecular architecture for dye-sensitized solar cells , 2012 .
[8] M. Kanatzidis,et al. All-solid-state dye-sensitized solar cells with high efficiency , 2012, Nature.
[9] John Kieffer,et al. Organic Dye Design Tools for Efficient Photocurrent Generation in Dye‐Sensitized Solar Cells: Exciton Binding Energy and Electron Acceptors , 2012 .
[10] Y. Chang,et al. Highly efficient triarylene conjugated dyes for sensitized solar cells , 2011 .
[11] F. Fabregat‐Santiago,et al. Characterization of nanostructured hybrid and organic solar cells by impedance spectroscopy. , 2011, Physical chemistry chemical physics : PCCP.
[12] Xin Li,et al. Organic D‐A‐π‐A Solar Cell Sensitizers with Improved Stability and Spectral Response , 2011 .
[13] K. Schanze,et al. Low-bandgap donor-acceptor conjugated polymer sensitizers for dye-sensitized solar cells. , 2011, Journal of the American Chemical Society.
[14] P. Chou,et al. Donor–acceptor dyes with fluorine substituted phenylene spacer for dye-sensitized solar cells , 2011 .
[15] Peng Wang,et al. High-efficiency dye-sensitized solar cells: the influence of lithium ions on exciton dissociation, charge recombination, and surface states. , 2010, ACS nano.
[16] P. Chou,et al. Organic dyes with remarkably high absorptivity; all solid-state dye sensitized solar cell and role of fluorine substitution. , 2010, Chemical communications.
[17] Eric A. Perpète,et al. Towards new efficient dye-sensitised solar cells , 2010 .
[18] Chulwoo Kim,et al. High molar extinction coefficient organic sensitizers for efficient dye-sensitized solar cells. , 2010, Chemistry.
[19] Anders Hagfeldt,et al. Characteristics of the iodide/triiodide redox mediator in dye-sensitized solar cells. , 2009, Accounts of chemical research.
[20] Jia-Hung Tsai,et al. Highly efficient light-harvesting ruthenium sensitizer for thin-film dye-sensitized solar cells. , 2009, ACS nano.
[21] Wenjun Wu,et al. Starburst triphenylamine-based cyanine dye for efficient quasi-solid-state dye-sensitized solar cells , 2009 .
[22] Nam-Gyu Park,et al. Selective positioning of organic dyes in a mesoporous inorganic oxide film. , 2009, Nature materials.
[23] M. Thelakkat,et al. Synthesis, spectral, electrochemical and photovoltaic properties of novel heteroleptic polypyridyl ruthenium(II) donor-antenna dyes , 2009 .
[24] Michael Grätzel,et al. High open-circuit voltage solid-state dye-sensitized solar cells with organic dye. , 2009, Nano letters.
[25] M. Fischer,et al. Metal-free organic dyes for dye-sensitized solar cells: from structure: property relationships to design rules. , 2009, Angewandte Chemie.
[26] Min Xu,et al. Conveniently synthesized isophorone dyes for high efficiency dye-sensitized solar cells: tuning photovoltaic performance by structural modification of donor group in donor-pi-acceptor system. , 2009, Chemical communications.
[27] Yongfang Li,et al. Poly(3,6-dihexyl-thieno[3,2-b]thiophene vinylene): Synthesis, Field-Effect Transistors, and Photovoltaic Properties , 2008 .
[28] Seigo Ito,et al. Bifacial dye-sensitized solar cells based on an ionic liquid electrolyte , 2008 .
[29] N. Park,et al. Size-dependent scattering efficiency in dye-sensitized solar cell , 2008 .
[30] Michael Grätzel,et al. Highly efficient and thermally stable organic sensitizers for solvent-free dye-sensitized solar cells. , 2008, Angewandte Chemie.
[31] N. Park,et al. On the I–V measurement of dye-sensitized solar cell: Effect of cell geometry on photovoltaic parameters , 2007 .
[32] Annabella Selloni,et al. Influence of the sensitizer adsorption mode on the open-circuit potential of dye-sensitized solar cells. , 2007, Nano letters.
[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] Guido Viscardi,et al. Combined experimental and DFT-TDDFT computational study of photoelectrochemical cell ruthenium sensitizers. , 2005, Journal of the American Chemical Society.
[35] Akihiro Furube,et al. Oligothiophene-containing coumarin dyes for efficient dye-sensitized solar cells. , 2005, The journal of physical chemistry. B.
[36] Juan Bisquert,et al. Influence of electrolyte in transport and recombination in dye-sensitized solar cells studied by impedance spectroscopy , 2005 .
[37] Hironori Arakawa,et al. Novel Conjugated Organic Dyes for Efficient Dye‐Sensitized Solar Cells , 2005 .
[38] Hironori Arakawa,et al. Molecular Design of Coumarin Dyes for Efficient Dye-Sensitized Solar Cells , 2003 .
[39] Marco-A. De Paoli,et al. Solid-State and Flexible Dye-Sensitized TiO2 Solar Cells: a Study by Electrochemical Impedance Spectroscopy , 2002 .
[40] M. Grätzel. Photoelectrochemical cells : Materials for clean energy , 2001 .
[41] Michael Grätzel,et al. Photoelectrochemical cells , 2001, Nature.
[42] Tetsuya Noda,et al. A Novel Class of Emitting Amorphous Molecular Materials as Bipolar Radical Formants: 2-{4-[Bis(4-methylphenyl)amino]phenyl}- 5-(dimesitylboryl)thiophene and 2-{4-[Bis(9,9-dimethylfluorenyl)amino]phenyl}- 5-(dimesitylboryl)thiophene , 2000 .
[43] A. Hagfeldt,et al. Molecular photovoltaics. , 2000, Accounts of chemical research.
[44] Mark A. Ratner,et al. 6-31G * basis set for atoms K through Zn , 1998 .
[45] Anders Hagfeldt,et al. Light-Induced Redox Reactions in Nanocrystalline Systems , 1995 .
[46] M. Frisch,et al. Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields , 1994 .
[47] M. Grätzel,et al. A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films , 1991, Nature.
[48] J. Pople,et al. Self‐Consistent Molecular‐Orbital Methods. IX. An Extended Gaussian‐Type Basis for Molecular‐Orbital Studies of Organic Molecules , 1971 .