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Effect of Tetrahydroquinoline Dyes Structure on the Performance of Organic Dye-Sensitized Solar Cells
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/adfm.200400272openalex-snapshot
Novel Conjugated Organic Dyes for Efficient Dye‐Sensitized Solar Cells
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Organic Dye for Highly Efficient Solid‐State Dye‐Sensitized Solar Cells
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The advent of mesoscopic injection solar cells
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Highly efficient metal-free organic dyes for dye-sensitized solar cells
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Highly efficient photon-to-electron conversion with mercurochrome-sensitized nanoporous oxide semiconductor solar cells
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Dye-sensitized nanocrystalline TiO2 solar cells based on novel coumarin dyes
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Nano-porous TiO2 photovoltaic cells sensitized with metallochromic triphenylmethane dyes: [n-TiO2/triphenylmethane dye/p-I−/I3− (or CuI)]
inferredcites →https://doi.org/10.1016/s1389-5567(03)00026-1openalex-snapshot
Dye-sensitized solar cells
inferredcites →https://doi.org/10.1021/cm011563sopenalex-snapshot
Quantitative Analysis of Light-Harvesting Efficiency and Electron-Transfer Yield in Ruthenium-Dye-Sensitized Nanocrystalline TiO2Solar Cells
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Phenyl-Conjugated Oligoene Sensitizers for TiO 2 Solar Cells
inferredcites →https://doi.org/10.1021/cr00017a013openalex-snapshot
Photochemistry on nonreactive and reactive (semiconductor) surfaces
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Light-Induced Redox Reactions in Nanocrystalline Systems
inferredcites →https://doi.org/10.1021/ic0508371openalex-snapshot
Solar Energy Conversion by Dye-Sensitized Photovoltaic Cells
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The Reaction of Acetone with Aniline
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Structure−Property Relationships of Donor/Acceptor-Functionalized Tetrakis(phenylethynyl)benzenes and Bis(dehydrobenzoannuleno)benzenes
inferredcites →https://doi.org/10.1021/ja0488277openalex-snapshot
High Efficiency of Dye-Sensitized Solar Cells Based on Metal-Free Indoline Dyes
inferredcites →https://doi.org/10.1021/ja0645640openalex-snapshot
Alkyl-Functionalized Organic Dyes for Efficient Molecular Photovoltaics
inferredcites →https://doi.org/10.1021/jo00811a016openalex-snapshot
Synthesis, oxidation, and electronic spectra of four dithienothiophenes
inferredcites →https://doi.org/10.1021/jo00811a017openalex-snapshot
Solvolyses of 2.alpha.,5-epithio-5.alpha.- and -epoxy-5.alpha.-cholestane derivatives. A reactivity factor of 1011 due to sulfur participation in a 7-thiabicyclo[2.2.1]heptane derivative
inferredcites →https://doi.org/10.1021/jo010713fopenalex-snapshot
Design and Synthesis of Push−Pull Chromophores for Second-Order Nonlinear Optics Derived from Rigidified Thiophene-Based π-Conjugating Spacers
inferredcites →https://doi.org/10.1021/jp0129380openalex-snapshot
Photoelectrochemical Properties of J Aggregates of Benzothiazole Merocyanine Dyes on a Nanostructured TiO2Film
inferredcites →https://doi.org/10.1021/jp0573339openalex-snapshot
STM Study of the Conformation and Reaction of Long-Chain Haloalkanes at Si(111)-7 × 7
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Infrared Spectroscopic Observation of the Group 13 Metal Hydroxides, M(OH) 1,2,3 (M =Al, Ga, In, and Tl) and HAl(OH) 2
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Dye Sensitization of Nanocrystalline Tin Oxide by Perylene Derivatives
inferredcites →https://doi.org/10.1021/la0357615openalex-snapshot
Effect of Additives on the Photovoltaic Performance of Coumarin-Dye-Sensitized Nanocrystalline TiO2Solar Cells
inferredcites →https://doi.org/10.1023/a:1017523701357openalex-snapshot
6-(1,3-Dioxoindan-2-ylidenemethyl)-1,2,2,4-tetramethyl-1,2-dihydro- and 1,2,3,4-Tetrahydroquinolines
inferredcites →https://doi.org/10.1039/a900075eopenalex-snapshot
Synthesis, polymerization and characterization of substituted dithieno[3,4-b:3′,4′-d]thiophenes
inferredcites →https://doi.org/10.1039/b203260kopenalex-snapshot
New perylenes for dye sensitization of TiO2
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Design of new coumarin dyes having thiophene moieties for highly efficient organic-dye-sensitized solar cells
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Self-Consistent Molecular-Orbital Methods. IX. An Extended Gaussian-Type Basis for Molecular-Orbital Studies of Organic Molecules
inferredcites →https://doi.org/10.1080/00397918108063618openalex-snapshot
The Palladium-Catalyzed Cross-Coupling Reaction of Phenylboronic Acid with Haloarenes in the Presence of Bases
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Synthesis, Characterization, and Computational Study of Azo Disperse Dyes Derived from 2-Nitroso-1-Napthol and 1-Nitroso-2-Naphthol with Other Commercial Dyes
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The McMurry Coupling and Related Reactions
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High‐Performance Organic Materials for Dye‐Sensitized Solar Cells: Triarylene‐Linked Dyads with a 4‐tert‐Butylphenylamine Donor
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High‐Performance Dye‐Sensitized Solar Cells Based on Phenothiazine Dyes Containing Double Anchors and Thiophene Spacers
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Double‐Anchored Triphenylamine‐Fluorene Functionalized Dyes for High‐Performance Photocatalytic Hydrogen Generation
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New Pyrrole‐Based Organic Dyes for Dye‐Sensitized Solar Cells: Convenient Syntheses and High Efficiency
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Organic Photovoltaic Devices Based on a New Class of Oligothienylenevinylene Derivatives as Donor Materials
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Efficient Synthesis of a Regioregular Oligothiophene Photovoltaic Dye Molecule, MK‐2, and Related Compounds: A Cooperative Hypervalent Iodine and Metal‐Catalyzed Synthetic Route
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inferred← citeshttps://doi.org/10.1002/cphc.201200064openalex-snapshot
Acene‐Modified Triphenylamine Dyes for Dye‐Sensitized Solar Cells: A Computational Study
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Photophysical and Electrochemical Properties, and Molecular Structures of Organic Dyes for Dye‐Sensitized Solar Cells
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Double D–π–A Dye Linked by 2,2′‐Bipyridine Dicarboxylic Acid: Influence of para‐ and meta‐Substituted Carboxyl Anchoring Group
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Triarylamine‐Substituted Imidazole‐ and Quinoxaline‐Fused Push–Pull Porphyrins for Dye‐Sensitized Solar Cells
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inferred← citeshttps://doi.org/10.1002/ejoc.200900236openalex-snapshot
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Trilateral π-conjugation extensions of phenothiazine-based dyes enhance the photovoltaic performance of the dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2017.11.045openalex-snapshot
Strategies to improve the performance of metal-free dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.09.035openalex-snapshot
Pyranylidene/thienothiophene-based organic sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.107945openalex-snapshot
A novel σ-linkage to dianchor dyes for efficient dyes sensitized solar cells: 3-methyl-1,1-cyclohexane
inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110700openalex-snapshot
Effect of seven different terthiophene π-spacers on dye performance in dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2026.113900openalex-snapshot
Enhanced photoconversion efficiency in a solar cell through the cooperative action of RK1 and MK-2 dyes: An electrochemical study
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2010.07.013openalex-snapshot
Hyperbranched conjugated polymers with donor-π-acceptor architecture as organic sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.ica.2018.01.021openalex-snapshot
Performance improvement of RuII complexes pyridinyl backbone on dye-sensitized solar cells (DSSC)
inferred← citeshttps://doi.org/10.1016/j.jcrysgro.2011.06.031openalex-snapshot
Effect of ethylene glycol on the growth of hexagonal SnS2 nanoplates and their optical properties
inferred← citeshttps://doi.org/10.1016/j.jechem.2015.10.016openalex-snapshot
Synthesis and photophysical properties of donor–acceptor system based bipyridylporphyrins for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2025.113190openalex-snapshot
Conjugation-driven modulation of excited-state dynamics and photobiological activity in Ru(II) bis-terpyridyl oligothienyl complexes
inferred← citeshttps://doi.org/10.1016/j.jlumin.2014.10.056openalex-snapshot
Assemblies composed of oligothiophene–ruthenium complexes bound to CdSe nanoparticles
inferred← citeshttps://doi.org/10.1016/j.jmgm.2021.107852openalex-snapshot
The chemical reactivity and QSPR of organic compounds applied to dye-sensitized solar cells using DFT
inferred← citeshttps://doi.org/10.1016/j.jmgm.2025.108968openalex-snapshot
Strategic control of electron donation in D-A-π-A dyes: Insights from DFT calculations for enhanced DSSC and NLO performance
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2013.09.006openalex-snapshot
Novel dye sensitizers of main chain polymeric metal complexes based on complexes of diaminomaleonitrile with Cd(II), Ni(II): Synthesis, characterization, and photovoltaic performance for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2011.08.001openalex-snapshot
Carbazole donor and carbazole or bithiophene bridged sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2022.113918openalex-snapshot
Synthesis, photophysical, electrochemical and computational studies of novel 2-aminoimidazolones with D-π-A framework
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2012.09.053openalex-snapshot
How to design more efficient organic dyes for dye-sensitized solar cells? Adding more sp2-hybridized nitrogen in the triphenylamine donor
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2013.03.018openalex-snapshot
Bulky dendritic triarylamine-based organic dyes for efficient co-adsorbent-free dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2013.03.091openalex-snapshot
Varied alkyl chain functionalized organic dyes for efficient dye-sensitized solar cells: Influence of alkyl substituent type on photovoltaic properties
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2013.05.188openalex-snapshot
Triphenylamine-based organic dyes with julolidine as the secondary electron donor for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2013.12.032openalex-snapshot
Effects of different alkyl chains on the performance of dye-sensitized solar cells with different electrolytes
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2014.05.079openalex-snapshot
Highly efficient light-harvesting boradiazaindacene sensitizers for dye-sensitized solar cells featuring phenothiazine donor antenna
inferred← citeshttps://doi.org/10.1016/j.molstruc.2017.01.078openalex-snapshot
Conformational landscape, stability, potential energy curves and vibrations of 1,2,3,4 tetrahydroquinoline
inferred← citeshttps://doi.org/10.1016/j.mseb.2009.01.033openalex-snapshot
Quasi solid state dye sensitized solar cells employing a polymer electrolyte and xanthene dyes
inferred← citeshttps://doi.org/10.1016/j.mseb.2014.04.010openalex-snapshot
Influence of annealing temperature and organic dyes as sensitizers on sol–gel derived TiO2 films
inferred← citeshttps://doi.org/10.1016/j.mtsust.2026.101455openalex-snapshot
Emerging architectures of halide perovskite based transistors for optoelectronic and neuromorphic systems
inferred← citeshttps://doi.org/10.1016/j.orgel.2010.05.002openalex-snapshot
Simple sensitizers of low band gap based on 4-nitro-α-cyanostilbene prepared from a one-step reaction for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.orgel.2011.08.010openalex-snapshot
Effects of aromatic π-conjugated bridges on optical and photovoltaic properties of N,N-diphenylhydrazone-based metal-free organic dyes
inferred← citeshttps://doi.org/10.1016/j.orgel.2014.09.003openalex-snapshot
Novel 4 H -pyranylidene organic dyes for dye-sensitized solar cells: Effect of different heteroaromatic rings on the photovoltaic properties
inferred← citeshttps://doi.org/10.1016/j.renene.2011.07.017openalex-snapshot
VIS harvesting unsymmetrical squaraine dye for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.rser.2024.114549openalex-snapshot
Dye-sensitized solar cells: Insights and research divergence towards alternatives
inferred← citeshttps://doi.org/10.1016/j.saa.2010.03.027openalex-snapshot
QSPR study of absorption maxima of organic dyes for dye-sensitized solar cells based on 3D descriptors
inferred← citeshttps://doi.org/10.1016/j.snb.2015.10.057openalex-snapshot
A turn-on fluorescent probe for cyanide based on aggregation of terthienyl and its application for bioimaging
inferred← citeshttps://doi.org/10.1016/j.solener.2010.07.009openalex-snapshot
Pomegranate leaves and mulberry fruit as natural sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.solener.2011.02.023openalex-snapshot
A nickel-complex sensitiser for dye-sensitised solar cells
inferred← citeshttps://doi.org/10.1016/j.solener.2019.05.051openalex-snapshot
Triple bond rigidified anthracene-triphenylamine sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.solener.2019.11.092openalex-snapshot
Theoretical screening of high-efficiency sensitizers with D-π-A framework for DSSCs by altering promising donor group
inferred← citeshttps://doi.org/10.1016/j.solener.2020.05.101openalex-snapshot
Dye-sensitized solar cells based on dimethylamino-π-bridge-pyranoanthocyanin dyes
inferred← citeshttps://doi.org/10.1016/j.solmat.2008.05.007openalex-snapshot
Red Sicilian orange and purple eggplant fruits as natural sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.solmat.2012.08.008openalex-snapshot
Surface passivation: The effects of CDCA co-adsorbent and dye bath solvent on the durability of dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.synthmet.2009.09.013openalex-snapshot
Effect of donor moiety in organic sensitizer on spectral response, electrochemical and photovoltaic properties
inferred← citeshttps://doi.org/10.1016/j.synthmet.2010.08.001openalex-snapshot
Synthesis and characterization of triphenylamine-based organic dyes for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.synthmet.2010.12.028openalex-snapshot
A novel main chain polymeric metal complex based on Zn(II) with thiophene and 2-(2′-pyridyl)benzimidazole ligand: Synthesis, characterization, photovoltaic property and application in DSSCs
inferred← citeshttps://doi.org/10.1016/j.synthmet.2011.03.022openalex-snapshot
Polypyridyl Ru(II)-sensitizers with extended π-system enhances the performance of dye sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.synthmet.2011.06.001openalex-snapshot
Novel 1,3,4-oxadiazole derivatives as efficient sensitizers for dye-sensitized solar cells: A combined experimental and computational study
inferred← citeshttps://doi.org/10.1016/j.synthmet.2014.02.019openalex-snapshot
N-Aryl group influences on the properties of umbrella-shaped thiophene-(N-aryl)pyrrole-thiophene dyes
inferred← citeshttps://doi.org/10.1016/j.tet.2009.09.036openalex-snapshot
Triaryl linked donor acceptor dyads for high-performance dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tet.2010.02.039openalex-snapshot
Novel polymeric metal complexes as dye sensitizers for Dye-sensitized solar cells based on poly thiophene containing complexes of 8-hydroxyquinoline with Zn(II),Cu(II) and Eu(III) in the side chain
inferred← citeshttps://doi.org/10.1016/j.tet.2010.02.095openalex-snapshot
Synthesis of sensitizers containing donor cascade of triarylamine and dimethylarylamine moieties for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tet.2010.09.004openalex-snapshot
Structure–property relationship of acceptor-substituted oligothiophenes
inferred← citeshttps://doi.org/10.1016/j.tet.2011.11.004openalex-snapshot
Engineering of highly efficient tetrahydroquinoline sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tet.2012.04.074openalex-snapshot
Functionalized organic dyes containing a phenanthroimidazole donor for dye-sensitized solar cell applications
inferred← citeshttps://doi.org/10.1016/j.tet.2012.06.064openalex-snapshot
Metal-free organic dyes for dye-sensitized solar cells: recent advances
inferred← citeshttps://doi.org/10.1016/j.tet.2013.08.075openalex-snapshot
Metal-free organic dyes with benzothiadiazole as an internal acceptor for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.050openalex-snapshot
Structural optimization of thiophene-(N-aryl)pyrrole-thiophene-based metal-free organic sensitizer for the enhanced dye-sensitized solar cell performance
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.072openalex-snapshot
Anthracene based organic dipolar compounds for sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tet.2014.02.002openalex-snapshot
N-Alkyl- and N-aryl-dithieno[3,2-b:2′,3′-d]pyrrole-containing organic dyes for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tet.2014.04.039openalex-snapshot
Synthesis and photovoltaic properties of new [1,2,5]thiadiazolo[3,4-c]pyridine-based organic Broadly absorbing sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tet.2015.06.047openalex-snapshot
Aldehyde end-capped terthiophene with aggregation-induced emission characteristics
inferred← citeshttps://doi.org/10.1016/j.tet.2017.04.037openalex-snapshot
The relationship between molecular structure and electronic properties in dicyanovinyl substituted acceptor-donor-acceptor chromophores
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.03.091openalex-snapshot
Thiophene-fused coplanar sensitizer for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.04.052openalex-snapshot
Synthesis and spectroscopic properties of ring-fused thiophene bridged push–pull dyes and their application in dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.theochem.2008.04.022openalex-snapshot
Theoretical studies of natural pigments relevant to dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.5c00449openalex-snapshot
Covalently Platinated DNA Oligonucleotides as Ratiometric Dioxygen Sensors
inferred← citeshttps://doi.org/10.1021/acs.iecr.0c00612openalex-snapshot
Highly Efficient Dye-Sensitized Solar Cells with Composited Food Dyes
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c03216openalex-snapshot
Ru(II) Phenanthroline-Based Oligothienyl Complexes as Phototherapy Agents
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.3c04382openalex-snapshot
Ru(II) Oligothienyl Complexes with Fluorinated Ligands: Photophysical, Electrochemical, and Photobiological Properties
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c03847openalex-snapshot
Hypoxia-Active Iridium(III) Bis-terpyridine Complexes Bearing Oligothienyl Substituents: Synthesis, Photophysics, and Phototoxicity toward Cancer Cells
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.8b00689openalex-snapshot
Cyclometalated Ruthenium(II) Complexes Derived from α-Oligothiophenes as Highly Selective Cytotoxic or Photocytotoxic Agents
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02481openalex-snapshot
Recent Progress in the Chemistry of Pyridazinones for Functional Group Transformations
inferred← citeshttps://doi.org/10.1021/acs.jpca.3c00671openalex-snapshot
Systematic Tuning of Electronic Ground and Excited States in Donor–Acceptor Dyes; Steps toward Designer Compounds for Modern Technologies
inferred← citeshttps://doi.org/10.1021/acs.jpcc.0c04119openalex-snapshot
Influence of Different Molecular Design Strategies on Photovoltaic Properties of a Series of Triphenylamine-Based Organic Dyes for Dye-Sensitized Solar Cells: Insights from Theoretical Investigations
inferred← citeshttps://doi.org/10.1021/acs.jpcc.5b09117openalex-snapshot
Computational Study on the Intramolecular Charge Separation of D-A-π-A Organic Sensitizers with Different Linker Groups
inferred← citeshttps://doi.org/10.1021/acs.jpcc.6b07032openalex-snapshot
Spacer Effects of Donor-π Spacer-Acceptor Sensitizers on Photophysical Properties in Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01302openalex-snapshot
Tetrahydroquinolines via Stereospecific [3 + 3]-Annulation of Donor–Acceptor Cyclopropanes with Nitrosoarenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03981openalex-snapshot
Synthesis of Carboxy ATTO 647N Using Redox Cycling for Xanthone Access
inferred← citeshttps://doi.org/10.1021/acsaem.3c00072openalex-snapshot
Densely Packed D−π–A Photosensitizers on TiO 2 Enable Efficient Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acsami.5b11554openalex-snapshot
Influence of Phenylethynylene of Push–Pull Zinc Porphyrins on the Photovoltaic Performance
inferred← citeshttps://doi.org/10.1021/acsenergylett.9b00141openalex-snapshot
13.6% Efficient Organic Dye-Sensitized Solar Cells by Minimizing Energy Losses of the Excited State
inferred← citeshttps://doi.org/10.1021/acsomega.0c01255openalex-snapshot
Photovoltaic Performance of 4,8-Bis(2′-ethylhexylthiophene)thieno[2,3- f ]benzofuran-Based Dyes Fabricated with Different Donors in Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acssuschemeng.5b00332openalex-snapshot
Unravel the Impact of Anchoring Groups on the Photovoltaic Performances of Diketopyrrolopyrrole Sensitizers for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/am301907zopenalex-snapshot
Comparative Interface Metrics for Metal-Free Monolayer-Based Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/am4010545openalex-snapshot
Molecular Design and Performance of Hydroxylpyridium Sensitizers for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/am402675qopenalex-snapshot
Novel Carbazole-Phenothiazine Dyads for Dye-Sensitized Solar Cells: A Combined Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1021/cm3036357openalex-snapshot
Molecular Engineering of Organic Dyes for Improved Recombination Lifetime in Solid-State Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/cm703459popenalex-snapshot
Ladder-Type Pentaphenylene Dyes for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/cr8004229openalex-snapshot
Functional Oligothiophenes: Molecular Design for Multidimensional Nanoarchitectures and Their Applications
inferred← citeshttps://doi.org/10.1021/ja803534uopenalex-snapshot
Interfacial Electron-Transfer Kinetics in Metal-Free Organic Dye-Sensitized Solar Cells: Combined Effects of Molecular Structure of Dyes and Electrolytes
inferred← citeshttps://doi.org/10.1021/jo800159topenalex-snapshot
Starburst Triarylamine Based Dyes for Efficient Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/jo8005182openalex-snapshot
Molecular Engineering of Organic Sensitizers Containing p-Phenylene Vinylene Unit for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/jp1004049openalex-snapshot
Effects of π-Elongation and the Fused Position of Quinoxaline-Fused Porphyrins as Sensitizers in Dye-Sensitized Solar Cells on Optical, Electrochemical, and Photovoltaic Properties
inferred← citeshttps://doi.org/10.1021/jp101238kopenalex-snapshot
Molecular Design of Anthracene-Bridged Metal-Free Organic Dyes for Efficient Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/jp101945zopenalex-snapshot
Novel Broadly Absorbing Sensitizers with Cyanovinylene 4-Nitrophenyl Segments and Various Anchoring Groups: Synthesis and Application for High-Efficiency Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/jp102486bopenalex-snapshot
Effects of meso-Diarylamino Group of Porphyrins as Sensitizers in Dye-Sensitized Solar Cells on Optical, Electrochemical, and Photovoltaic Properties
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