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Effect of Extended π-Conjugation of the Donor Structure of Organic D–A−π–A Dyes on the Photovoltaic Performance of Dye-Sensitized Solar Cells
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adfm.201001801openalex-snapshot
Organic D‐A‐π‐A Solar Cell Sensitizers with Improved Stability and Spectral Response
inferredcites →https://doi.org/10.1002/adfm.201102519openalex-snapshot
Significant Improvement of Dye‐Sensitized Solar Cell Performance by Small Structural Modification in π‐Conjugated Donor–Acceptor Dyes
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Molecular Engineering of Push–Pull Porphyrin Dyes for Highly Efficient Dye‐Sensitized Solar Cells: The Role of Benzene Spacers
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Benzothiadiazole Containing D‐π‐A Conjugated Compounds for Dye‐Sensitized Solar Cells: Synthesis, Properties, and Photovoltaic Performances
inferredcites →https://doi.org/10.1002/chem.201204343openalex-snapshot
Molecular Design Principle of All‐organic Dyes for Dye‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1016/j.jphotochem.2009.01.017openalex-snapshot
Photovoltaic performance of dye-sensitized solar cells based on a series of new-type donor–acceptor π-conjugated sensitizer, benzofuro[2,3-c]oxazolo[4,5-a]carbazole fluorescent dyes
inferredcites →https://doi.org/10.1016/j.tet.2006.12.082openalex-snapshot
Molecular engineering of organic dyes containing N-aryl carbazole moiety for solar cell
inferredcites →https://doi.org/10.1016/j.tet.2009.04.024openalex-snapshot
Dye-sensitized solar cell utilizing organic dyads containing triarylene conjugates
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Phenyl-Conjugated Oligoene Sensitizers for TiO 2 Solar Cells
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Hexylthiophene-Functionalized Carbazole Dyes for Efficient Molecular Photovoltaics: Tuning of Solar-Cell Performance by Structural Modification
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Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields
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High Efficiency of Dye-Sensitized Solar Cells Based on Metal-Free Indoline Dyes
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Alkyl-Functionalized Organic Dyes for Efficient Molecular Photovoltaics
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Molecular Engineering of Organic Sensitizers for Dye-Sensitized Solar Cell Applications
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Synthesis and Photovoltaic Properties of Efficient Organic Dyes Containing the Benzo[b]furan Moiety for Solar Cells
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Starburst Triarylamine Based Dyes for Efficient Dye-Sensitized Solar Cells
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Enhanced Energy and Quantum Efficiencies of a Nanocrystalline Photoelectrochemical Cell Sensitized with a Donor−Acceptor Dyad Derived from Fluorescein
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Lithium Ion Effect on Electron Injection from a Photoexcited Coumarin Derivative into a TiO2 Nanocrystalline Film Investigated by Visible-to-IR Ultrafast Spectroscopy
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Molecular Design of Coumarin Dyes for Stable and Efficient Organic Dye-Sensitized Solar Cells
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Simple Triarylamine-Based Dyes Containing Fluorene and Biphenyl Linkers for Efficient Dye-Sensitized Solar Cells
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Unsymmetrical Squaraines Incorporating the Thiophene Unit for Panchromatic Dye-Sensitized Solar Cells
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inferredcites →https://doi.org/10.1039/c2cs35346fopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c2ee22108jopenalex-snapshot
High-conversion-efficiency organic dye-sensitized solar cells: molecular engineering on D–A–π-A featured organic indoline dyes
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6-31G* basis set for atoms K through Zn
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Porphyrin-Sensitized Solar Cells with Cobalt (II/III)–Based Redox Electrolyte Exceed 12 Percent Efficiency
inferredcites →https://doi.org/10.1246/cl.1998.753openalex-snapshot
Photosensitization of Porous TiO2 Semiconductor Electrode with Xanthene Dyes
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.dyepig.2015.05.012openalex-snapshot
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