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Efficient Structural Modification of Triphenylamine-Based Organic Dyes for Dye-Sensitized Solar Cells
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Novel Indolenine-Based hemicyanine dyes with extended π-Linker and auxiliary donor as potential Photosensitizers: Synthesis, Photophysical, electrochemical and computational Insights
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Enhancing the performance of dye-sensitized solar cells based on organic dye sensitized TiO 2 nanoparticles/nanowires composite photoanodes with ionic liquid electrolyte
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.129208openalex-snapshot
Solvent free and green synthesis of efficient solvochromism based coumarin moieties for quick visualization of LFPs and OLEDs applications
inferred← citeshttps://doi.org/10.1016/j.orgel.2015.06.033openalex-snapshot
Investigation of benzo(1,2-b:4,5-b′)dithiophene as a spacer in organic dyes for high efficient dye-sensitized solar cell
inferred← citeshttps://doi.org/10.1016/j.orgel.2018.04.048openalex-snapshot
Rational design of cost-effective dyes for high performance dye-sensitized cells in indoor light environments
inferred← citeshttps://doi.org/10.1016/j.saa.2015.03.032openalex-snapshot
Bi-anchoring organic sensitizers of type D-(π-A) 2 comprising thiophene-2-acetonitrile as π-spacer and malonic acid as electron acceptor for dye sensitized solar cell applications
inferred← citeshttps://doi.org/10.1016/j.saa.2017.01.048openalex-snapshot
New dyes for DSSC containing triphenylamine based extended donor: Synthesis, photophysical properties and device performance
inferred← citeshttps://doi.org/10.1016/j.snb.2019.04.123openalex-snapshot
A signal-on detection of organophosphorus pesticides by fluorescent probe based on aggregation-induced emission
inferred← citeshttps://doi.org/10.1016/j.solener.2015.11.015openalex-snapshot
Triphenylamine based dyes for dye sensitized solar cells: A review
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.2012.09.018openalex-snapshot
Influences of the electron donor groups on the properties of thiophene-(N-aryl)pyrrole-thiophene-based organic sensitizers
inferred← citeshttps://doi.org/10.1016/j.synthmet.2015.03.033openalex-snapshot
Novel organic dyes based on diarylmethylene-bridged triphenylamine for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.synthmet.2015.10.024openalex-snapshot
Indole-based organic dyes with different electron donors for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.synthmet.2016.05.012openalex-snapshot
Synthesis and evaluation of simple molecules for dye sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.038openalex-snapshot
Dipolar organic pyridyl dyes for dye-sensitized solar cell applications
inferred← citeshttps://doi.org/10.1016/j.tet.2012.04.104openalex-snapshot
Synthesis of triphenylamine-based thiophene-(N-aryl)pyrrole-thiophene dyes for dye-sensitized solar cell applications
inferred← citeshttps://doi.org/10.1016/j.tet.2012.08.027openalex-snapshot
Macrocyclic triphenylamine based organic dyes for efficient 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.2015.04.089openalex-snapshot
Benzothiadiazole-based organic dyes with pyridine anchors for dye-sensitized solar cells: effect of donor on optical properties
inferred← citeshttps://doi.org/10.1016/j.tet.2018.04.043openalex-snapshot
Azulene – Thiophene – Cyanoacrylic acid dyes with donor-π-acceptor structures. Synthesis, characterisation and evaluation in dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.theochem.2009.06.010openalex-snapshot
Structures and excitation energies of Zn–tetraarylporphyrin analogues: A theoretical study
inferred← citeshttps://doi.org/10.1016/s1003-6326(10)60114-8openalex-snapshot
Naphthalene-containing polyimides: Synthesis, characterization and photovoltaic properties of novel donor-acceptor dyes used in solar cell
inferred← citeshttps://doi.org/10.1016/s1452-3981(23)06564-1openalex-snapshot
Structure Modification to Tune the Electronic and Charge Transport Properties of Solar Cell Materials: Quantum Chemical Study
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.8b03005openalex-snapshot
Systematic Control of the Overlapping Energy Region for an Efficient Intramolecular Energy Transfer: Functionalized Salen–Al/Triphenylamine Guest–Host Assemblies
inferred← citeshttps://doi.org/10.1021/acs.jchemed.2c00261openalex-snapshot
Synthesis and Characterization of a Metal-Free Organic Dye-Sensitizer for Solar Cell: An Advanced Organic Chemistry Research-Based Laboratory
inferred← citeshttps://doi.org/10.1021/acs.joc.5b02590openalex-snapshot
Benzimidazole-Branched Isomeric Dyes: Effect of Molecular Constitution on Photophysical, Electrochemical, and Photovoltaic Properties
inferred← citeshttps://doi.org/10.1021/acs.jpca.8b09048openalex-snapshot
Photoannealing of Merocyanine Aggregates
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02246openalex-snapshot
Palladium(II)-Catalyzed Direct C–H Alkenylation of Thienothiophene and Related Fused Heteroarenes
inferred← citeshttps://doi.org/10.1021/acsami.6b00226openalex-snapshot
Different Effect of the Additional Electron-Withdrawing Cyano Group in Different Conjugation Bridge: The Adjusted Molecular Energy Levels and Largely Improved Photovoltaic Performance
inferred← citeshttps://doi.org/10.1021/acsomega.3c08165openalex-snapshot
Design and Exploration by Quantum Chemical Analysis of Photosensitizers Having [D−π–π–A]- and [D-D-triad-A]-Type Molecular Structure Models for DSSC
inferred← citeshttps://doi.org/10.1021/am401201qopenalex-snapshot
Porphyrin-Sensitized Solar Cells: Effect of Carboxyl Anchor Group Orientation on the Cell Performance
inferred← citeshttps://doi.org/10.1021/cr8004229openalex-snapshot
Functional Oligothiophenes: Molecular Design for Multidimensional Nanoarchitectures and Their Applications
inferred← citeshttps://doi.org/10.1021/es100920jopenalex-snapshot
Design of New Triphenylamine-Sensitized Solar Cells: A Theoretical Approach
inferred← citeshttps://doi.org/10.1021/ja900612gopenalex-snapshot
Photoinduced Charge Transfer and Electrochemical Properties of Triphenylamine Ih-Sc3N@C80 Donor−Acceptor Conjugates
inferred← citeshttps://doi.org/10.1021/jo201057bopenalex-snapshot
Organic Dye Bearing Asymmetric Double Donor-π-Acceptor Chains for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/jp1050035openalex-snapshot
Photoinduced Energy-Transfer and Electron-Transfer Processes in Dye-Sensitized Solar Cells: TDDFT Insights for Triphenylamine Dyes
inferred← citeshttps://doi.org/10.1021/jp107439dopenalex-snapshot
Organic Dyes Incorporating Bis-hexapropyltruxeneamino Moiety for Efficient Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/jp302145xopenalex-snapshot
Effects of Porphyrinic meso-Substituents on the Photovoltaic Performance of Dye-Sensitized Solar Cells: Number and Position of p-Carboxyphenyl and Thienyl Groups on Zinc Porphyrins
inferred← citeshttps://doi.org/10.1021/jp304489topenalex-snapshot
D–D−π–A-Type Organic Dyes for Dye-Sensitized Solar Cells with a Potential for Direct Electron Injection and a High Extinction Coefficient: Synthesis, Characterization, and Theoretical Investigation
inferred← citeshttps://doi.org/10.1021/jp305884uopenalex-snapshot
Fluorous Molecules for Dye-Sensitized Solar Cells: Synthesis and Characterization of Fluorene-Bridged Donor/Acceptor Dyes with Bulky Perfluoroalkoxy Substituents
inferred← citeshttps://doi.org/10.1021/jp400336ropenalex-snapshot
Role of Adsorption Structures of Zn-Porphyrin on TiO2 in Dye-Sensitized Solar Cells Studied by Sum Frequency Generation Vibrational Spectroscopy and Ultrafast Spectroscopy
inferred← citeshttps://doi.org/10.1021/jp5049953openalex-snapshot
Design of Efficient Metal-Free Organic Dyes Having an Azacyclazine Scaffold as the Donor Fragment for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/jp808275zopenalex-snapshot
Energy-Level and Molecular Engineering of Organic D-π-A Sensitizers in Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/jp904946aopenalex-snapshot
Enhanced Efficiency of Organic Dye-Sensitized Solar Cells: Triphenylamine Derivatives
inferred← citeshttps://doi.org/10.1021/jp911139xopenalex-snapshot
High Molar Extinction Coefficient Branchlike Organic Dyes Containing Di(p-tolyl)phenylamine Donor for Dye-Sensitized Solar Cells Applications
inferred← citeshttps://doi.org/10.1021/jp911630zopenalex-snapshot
Effect of Cations in Coadsorbate on Charge Recombination and Conduction Band Edge Movement in Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/ol301730copenalex-snapshot
Fine-tuning the Electronic Structure of Organic Dyes for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/sc400293vopenalex-snapshot
Influence of Donor Configurations on Photophysical, Electrochemical, and Photovoltaic Performances in D−π–A Organic Sensitizers
inferred← citeshttps://doi.org/10.1039/b815649bopenalex-snapshot
Molecular design of triarylamine-based organic dyes for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/b822190aopenalex-snapshot
Novel TPD-based organic D–π–A dyes for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/b906687jopenalex-snapshot
A novel ruthenium-free TiO2 sensitizer consisting of di-p-tolylaminophenyl ethylenedioxythiophene and cyanoacrylate groups
inferred← citeshttps://doi.org/10.1039/b908802dopenalex-snapshot
Triarylamine: a promising core unit for efficient photovoltaic materials
inferred← citeshttps://doi.org/10.1039/c000474jopenalex-snapshot
Towards new efficient dye-sensitised solar cells
inferred← citeshttps://doi.org/10.1039/c003841eopenalex-snapshot
Improvement of dye-sensitized solar cells: what we know and what we need to know
inferred← citeshttps://doi.org/10.1039/c0dt00199fopenalex-snapshot
Spectral and redox properties of zinc porphyrin core dendrimers with triarylamines as dendron
inferred← citeshttps://doi.org/10.1039/c0nj00585aopenalex-snapshot
New molecular design of donor-π-acceptor dyes for dye-sensitized solar cells: control of molecular orientation and arrangement on TiO 2 surface
inferred← citeshttps://doi.org/10.1039/c1cc11130bopenalex-snapshot
Preparation of donor–acceptor type organic dyes bearing various electron-withdrawing groups for dye-sensitized solar cell application
inferred← citeshttps://doi.org/10.1039/c1ee01638eopenalex-snapshot
Investigation of the photoinduced electron injection processes for p-type triphenylamine-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c2cc17079eopenalex-snapshot
Spirally configured cis-stilbene/fluorene hybrids as bipolar, organic sensitizers for solar cell applications
inferred← citeshttps://doi.org/10.1039/c2jm30254copenalex-snapshot
Metal-free organic dyes derived from triphenylethylene for dye-sensitized solar cells: tuning of the performance by phenothiazine and carbazole
inferred← citeshttps://doi.org/10.1039/c2ra20777jopenalex-snapshot
New organic dyes containing tert-Butyl-capped N-Arylcarbazole moiety for Dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c3cc41861hopenalex-snapshot
Circle chain embracing donor–acceptor organic dye: simultaneous improvement of photocurrent and photovoltage for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c3cp51019kopenalex-snapshot
Electronic and optical properties of the triphenylamine-based organic dye sensitized TiO2 semiconductor: insight from first principles calculations
inferred← citeshttps://doi.org/10.1039/c3ee24453aopenalex-snapshot
Highly efficient dye-sensitized solar cells: progress and future challenges
inferred← citeshttps://doi.org/10.1039/c3ra41816bopenalex-snapshot
TDDFT studies of electronic spectra and excited states of the triphenylamine-based organic sensitizers and organic sensitizer–titanium dioxide cluster complexes
inferred← citeshttps://doi.org/10.1039/c3ta10423kopenalex-snapshot
Fluorine–thiophene-substituted organic dyes for dye sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c3ta11870copenalex-snapshot
D–π–A structured porphyrins for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c3ta12901bopenalex-snapshot
Dye-sensitized solar cells based on organic dyes with naphtho[2,1- b :3,4- b ′]dithiophene as the conjugated linker
inferred← citeshttps://doi.org/10.1039/c3ta15456dopenalex-snapshot
Organic dyes containing fluoren-9-ylidene chromophores for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c4qo00285gopenalex-snapshot
Thieno[2,3,a]carbazole donor-based organic dyes for high efficiency dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c4ra09300copenalex-snapshot
Functional tuning of phenothiazine-based dyes by a benzimidazole auxiliary chromophore: an account of optical and photovoltaic studies
inferred← citeshttps://doi.org/10.1039/c4ra15234dopenalex-snapshot
Functional tuning of organic dyes containing 2,7-carbazole and other electron-rich segments in the conjugation pathway
inferred← citeshttps://doi.org/10.1039/c4ta02161dopenalex-snapshot
New organic dyes based on a dibenzofulvene bridge for highly efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c5ra05287dopenalex-snapshot
A D–π–A–π–A type dye for highly efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c5ra15100gopenalex-snapshot
New thieno[3,2-b][1]benzothiophene-based organic sensitizers containing π-extended thiophene spacers for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c6ra06247dopenalex-snapshot
Efficient dye-sensitized solar cells with broad absorption and enhanced photo-current generation
inferred← citeshttps://doi.org/10.1039/c8cp06314aopenalex-snapshot
Excited state C–N bond dissociation and cyclization of tri-aryl amine-based OLED materials: a theoretical investigation
inferred← citeshttps://doi.org/10.1039/c8tc02017eopenalex-snapshot
Unsymmetrical starburst triarylamines: synthesis, properties, and characteristics of OFETs
inferred← citeshttps://doi.org/10.1039/d1nj02714jopenalex-snapshot
Computational study of 4,4′-dimethoxy triphenylamine donor linked with low band gap π-spacers by single and double bonds for DSSC applications
inferred← citeshttps://doi.org/10.1070/rc2009v078n02abeh003900openalex-snapshot
Merocyanine dyes: synthesis, structure, properties and applications
inferred← citeshttps://doi.org/10.1103/physrevb.84.245115openalex-snapshot
Electronic structure of dye-sensitized TiO 2 clusters from many-body perturbation theory
inferred← citeshttps://doi.org/10.1155/2014/548914openalex-snapshot
Steric and Solvent Effect in Dye-Sensitized Solar Cells Utilizing Phenothiazine-Based Dyes
inferred← citeshttps://doi.org/10.1246/bcsj.20100098openalex-snapshot
Dye-Sensitized Solar Cells Based on D–π–A Fluorescent Dyes with Pyridine Ring Forming Strong Interaction with Nanocrystalline TiO2
inferred← citeshttps://doi.org/10.1246/cl.151101openalex-snapshot
Linear and Tripodal Squaraine Sensitizers with Triphenylamine Donor Components for Dye-sensitized Solar Cells
inferred← citeshttps://doi.org/10.1246/cl.160242openalex-snapshot
Effect of Hexylthiophene and Hexyloxy Substituents on Triphenylamine-based DSSCs after TiCl4Treatment
inferred← citeshttps://doi.org/10.1246/cl.2012.1560openalex-snapshot
Novel 4-Trifluoromethylthiazole-5-carboxylic Acid as Acceptor in Photosensitized Dyes
inferred← citeshttps://doi.org/10.12794/metadc407837openalex-snapshot
Substitution Effects of Phenothiazine and Porphyrin Dyes in Dye-sensitized Solar Cells
inferred← citeshttps://doi.org/10.14233/ajchem.2021.23427openalex-snapshot
Comparative Study of Counter Electrodes Affecting the Conversion Efficiency in Fabrication of Dye Sensitized Solar Cell using Mixture of Dyes in Different Solvents
inferred← citeshttps://doi.org/10.2991/ap3er-15.2015.25openalex-snapshot
Synthesis of a Dye Containing Benzothiadiazole for Highly Efficient Dye-sensitized Solar Cells
inferred← citeshttps://doi.org/10.31590/ejosat.1118274openalex-snapshot
Karbazol Temelli (D–π–A) Duyarlaştırıcı: Sentezi, Karakterizasyonu ve DSSC Uygulaması
inferred← citeshttps://doi.org/10.32657/10356/44003openalex-snapshot
Enhancing the conversion effeciency of dye-sensitized solar cells (DSSCS) by optimizing the photoanode and dye
inferred← citeshttps://doi.org/10.3390/molecules23020421openalex-snapshot
Modulation of Donor-Acceptor Distance in a Series of Carbazole Push-Pull Dyes; A Spectroscopic and Computational Study
inferred← citeshttps://doi.org/10.3390/polym6102645openalex-snapshot
Fused-Thiophene Based Materials for Organic Photovoltaics and Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.4236/msce.2018.67004openalex-snapshot
Performance Improvement of Dye-Sensitized Solar Cell by Phenanthrothiadiazole Unit-Based π-Conjugated Bridge
inferred← citeshttps://doi.org/10.48138/cjo.943191openalex-snapshot
Boyaya Duyarlı Güneş Pillerinde Trifenilamin Tabanlı Organik Boyaların Kuantum Kimyasal Hesaplamaları
inferred← citeshttps://doi.org/10.5012/bkcs.2009.30.5.1157openalex-snapshot
Crystal Structures and Luminescence Properties of Pd(II) and Pt(II) Complexes with 2,5-Bis(thiophene)-1-nonyl-3,4-bis(methylthio)pyrrole
inferred← citeshttps://doi.org/10.5012/bkcs.2013.34.7.2093openalex-snapshot
Quantum Chemical Designing of Efficient Sensitizers for Dye Sensitized Solar Cells
inferred← citeshttps://doi.org/10.70675/374996d1z13c7z4be0za8a2zafdbc5a8536copenalex-snapshot
Approches théoriques pour les cellules photovoltaïques : étude des effets de substitution, du greffage et de la géométrie sur les propriétés optiques des sensibilisateurs
inferred← citeshttps://doi.org/10.70675/a4f1ecfez13a3z4efbza4fez5c45dea2da99openalex-snapshot
Ultrafast dynamics of excitons and charge carriers in colloidal perovskite nanostructures studied by time-resolved optical spectroscopies
inferred← citeshttps://doi.org/10.7598/cst2016.1191openalex-snapshot
Effect of Inserting Azabenzenes Linkers into TPA-Based Dye Sensitizers for Use in Solar Cells: DFT and TDDFT Calculations
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