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The Influence of Substituent Orientation on the Photovoltaic Performance of Phthalocyanine‐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/(sici)1521-3765(19980904)4:9<1633::aid-chem1633>3.0.co;2-oopenalex-snapshot
The Synthesis of Some Phthalocyanines and Napthalocyanines Derived from Sterically Hindered Phenols
inferredcites →https://doi.org/10.1002/ajoc.201402117openalex-snapshot
Light‐Harvesting in the Near‐Infrared Region: Dye‐Sensitized Solar Cells Sensitized with Asymmetric Ring‐Expanded Zinc(II) Phthalocyanines
inferredcites →https://doi.org/10.1002/ange.200603098openalex-snapshot
Efficient Sensitization of Nanocrystalline TiO2 Films by a Near‐IR‐Absorbing Unsymmetrical Zinc Phthalocyanine
inferredcites →https://doi.org/10.1002/ange.200703106openalex-snapshot
Molecular Cosensitization for Efficient Panchromatic Dye‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1002/ange.201105950openalex-snapshot
Molecular Engineering of Zinc Phthalocyanines with Phosphinic Acid Anchoring Groups
inferredcites →https://doi.org/10.1002/ange.201108610openalex-snapshot
Dye Molecules for Simple Co‐Sensitization Process: Fabrication of Mixed‐Dye‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1002/ange.201108963openalex-snapshot
Carboxyethynyl Anchoring Ligands: A Means to Improving the Efficiency of Phthalocyanine‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1002/anie.200603098openalex-snapshot
Efficient Sensitization of Nanocrystalline TiO2 Films by a Near‐IR‐Absorbing Unsymmetrical Zinc Phthalocyanine
inferredcites →https://doi.org/10.1002/anie.200703106openalex-snapshot
Molecular Cosensitization for Efficient Panchromatic Dye‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1002/anie.201105950openalex-snapshot
Molecular Engineering of Zinc Phthalocyanines with Phosphinic Acid Anchoring Groups
inferredcites →https://doi.org/10.1002/anie.201108610openalex-snapshot
Dye Molecules for Simple Co‐Sensitization Process: Fabrication of Mixed‐Dye‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1002/anie.201108963openalex-snapshot
Carboxyethynyl Anchoring Ligands: A Means to Improving the Efficiency of Phthalocyanine‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1002/chem.200500176openalex-snapshot
Deformed Phthalocyanines: Synthesis and Characterization of Zinc Phthalocyanines Bearing Phenyl Substituents at the 1‐, 4‐, 8‐, 11‐, 15‐, 18‐, 22‐, and/or 25‐Positions
inferredcites →https://doi.org/10.1002/chem.201300716openalex-snapshot
Molecular Design Rule of Phthalocyanine Dyes for Highly Efficient Near‐IR Performance in Dye‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1002/cphc.201301118openalex-snapshot
Sterically Hindered Phthalocyanines for Dye‐Sensitized Solar Cells: Influence of the Distance between the Aromatic Core and the Anchoring Group
inferredcites →https://doi.org/10.1002/ejoc.201301009openalex-snapshot
Recent Advances in Phthalocyanine‐Based Sensitizers for Dye‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1016/j.ica.2013.07.052openalex-snapshot
Near-infrared absorbing unsymmetrical Zn(II) phthalocyanine for dye-sensitized solar cells
inferredcites →https://doi.org/10.1016/j.jfluchem.2014.09.012openalex-snapshot
Synthesis and property of novel phthalocyanine having a 3,5-bis-pentafluorosulfanylphenyl group on the α-peripheral position
inferredcites →https://doi.org/10.1016/j.solmat.2007.05.004openalex-snapshot
Unsymmetrical alkoxy zinc phthalocyanine for sensitization of nanocrystalline TiO2 films
inferredcites →https://doi.org/10.1021/cr5001964openalex-snapshot
Meso-Substituted Porphyrins for Dye-Sensitized Solar Cells
inferredcites →https://doi.org/10.1021/ja0113753openalex-snapshot
Extremely Non-Planar Phthalocyanines with Saddle or Helical Conformation: Synthesis and Structural Characterizations
inferredcites →https://doi.org/10.1021/ja9109677openalex-snapshot
Enhancement of Incident Photon-to-Current Conversion Efficiency for Phthalocyanine-Sensitized Solar Cells by 3D Molecular Structuralization
inferredcites →https://doi.org/10.1021/jo100766hopenalex-snapshot
Synthesis and Characterization of Monoisomeric 1,8,15,22-Substituted (A3B and A2B2) Phthalocyanines and Phthalocyanine−Fullerene Dyads
inferredcites →https://doi.org/10.1021/jp908552topenalex-snapshot
Structural Modification of Organic Dyes for Efficient Coadsorbent-Free Dye-Sensitized Solar Cells
inferredcites →https://doi.org/10.1021/ol503557copenalex-snapshot
Convergent Strategy for the Regioselective Synthesis of Nonaggregated α-Triaryl-β-carboxy Zinc Phthalocyanines
inferredcites →https://doi.org/10.1038/nchem.1861openalex-snapshot
Dye-sensitized solar cells with 13% efficiency achieved through the molecular engineering of porphyrin sensitizers
inferredcites →https://doi.org/10.1039/b911397popenalex-snapshot
Symmetric and unsymmetric donor functionalization. comparing structural and spectral benefits of chromophores for dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c0cc02213fopenalex-snapshot
Lighting porphyrins and phthalocyanines for molecular photovoltaics
inferredcites →https://doi.org/10.1039/c3cc47714bopenalex-snapshot
Molecular engineering of zinc phthalocyanine sensitizers for efficient dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c3ra45170dopenalex-snapshot
Emerging molecular design strategies of unsymmetrical phthalocyanines for dye-sensitized solar cell applications
inferredcites →https://doi.org/10.1039/c4cs00309hopenalex-snapshot
Vegetable-based dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c4ta01894jopenalex-snapshot
Advances in phthalocyanine-sensitized solar cells (PcSSCs)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4791694openalex-extracted
Photovoltaic Performance Enhancement Via Cocktail Co-Sensitization of D–A–Π–A and D–Π–A–Π–A Dyes in Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1002/cplu.201600325openalex-snapshot
Role of the Bulky Aryloxy Group at the Non‐Peripheral Position of Phthalocyanines for Dye Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1016/j.ccr.2018.10.007openalex-snapshot
Phthalocyanines for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2024.112317openalex-snapshot
Photovoltaic performance enhancement via cocktail co-sensitization of D–A–π–A and D–π–A–π–A dyes in dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.electacta.2016.11.052openalex-snapshot
Soluble tetratriphenylamine Zn phthalocyanine as Hole Transporting Material for Perovskite Solar Cells
inferred← citeshttps://doi.org/10.1016/j.jclepro.2020.122236openalex-snapshot
Enhanced phthalocyanine-sensitized solar cell efficiency via cooperation of nitrogen-doped carbon dots
inferred← citeshttps://doi.org/10.1016/j.jpcs.2017.05.018openalex-snapshot
Polyoxometalate-modified TiO 2 nanotube arrays photoanode materials for enhanced dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.synthmet.2018.09.004openalex-snapshot
Synthesis, characterization and ethanol sensing properties of carboxylic acid-terminated naphthoxy substituted phthalocyanines
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00070openalex-snapshot
Wide-Range Near-Infrared Sensitizing 1H-Benzo[c,d]indol-2-ylidene-Based Squaraine Dyes for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acs.jpcc.7b01562openalex-snapshot
Photoinduced Electron Injection from Zinc Phthalocyanines into Zinc Oxide Nanorods: Aggregation Effects
inferred← citeshttps://doi.org/10.1021/acs.nanolett.7b02471openalex-snapshot
Monitoring Charge Separation Processes in Quasi-One-Dimensional Organic Crystalline Structures
inferred← citeshttps://doi.org/10.1021/acsomega.8b00600openalex-snapshot
Effect of Co-Adsorbate and Hole Transporting Layer on the Photoinduced Charge Separation at the TiO2–Phthalocyanine Interface
inferred← citeshttps://doi.org/10.1039/c6cp06513aopenalex-snapshot
Development of type-I/type-II hybrid dye sensitizer with both pyridyl group and catechol unit as anchoring group for type-I/type-II dye-sensitized solar cell
inferred← citeshttps://doi.org/10.1039/c6cp07386gopenalex-snapshot
Impact of the molecular structure and adsorption mode of D–π–A dye sensitizers with a pyridyl group in dye-sensitized solar cells on the adsorption equilibrium constant for dye-adsorption on TiO 2 surface
inferred← citeshttps://doi.org/10.1039/c7nj02057kopenalex-snapshot
Synthesis, the electronic properties and efficient photoinduced electron transfer of new pyrrolidine[60]fullerene- and isoxazoline[60]fullerene-BODIPY dyads: nitrile oxide cycloaddition under mild conditions using PIFA
inferred← citeshttps://doi.org/10.1039/c7ra00799jopenalex-snapshot
Synthesis, optical and electrochemical properties, and photovoltaic performance of a panchromatic and near-infrared (D) 2 –π–A type BODIPY dye with pyridyl group or cyanoacrylic acid
inferred← citeshttps://doi.org/10.1039/c8nj04672gopenalex-snapshot
Synthesis of near-infrared absorbing and fluorescing thiophene-fused BODIPY dyes with strong electron-donating groups and their application in dye-sensitised solar cells
inferred← citeshttps://doi.org/10.1039/d0cc03161eopenalex-snapshot
Iridium-catalysed 3,5-bis-borylation of phthalonitrile enables access to a family of C 4h octaarylphthalocyanines
inferred← citeshttps://doi.org/10.1134/s2070205118020090openalex-snapshot
New Hybrid Materials Based on Nanostructured Aluminum Oxyhydroxide and Terbium(III) Bis(Tetra-15-Crown-5-Phthalocyaninate)
inferred← citeshttps://doi.org/10.1142/s1088424616501121openalex-snapshot
Introducing rigid π-conjugated peripheral substituents in phthalocyanines for DSSCs
inferred← citeshttps://doi.org/10.1142/s1088424624500469openalex-snapshot
The role of spacer heteroatomic fragment in spectroscopic and luminescent behaviour of phenyl-substituted phthalocyanine complexes
inferred← citeshttps://doi.org/10.15407/ujpe64.1.63openalex-snapshot
Photoreactions of Macrocyclic Dyes on (1010) Wurtzite Surface – Interplay Between Conformation and Electronic Effects
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