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Effect of Five-Membered Heteroaromatic Linkers to the Performance of Phenothiazine-Based 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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1,5-Type nonbonded O⋯S and S⋯S interactions in (acylimino) and (thioacylimino)benzothiazoline systems. Crystal structures and theoretical calculations
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A High Molar Extinction Coefficient Sensitizer for Stable Dye-Sensitized Solar Cells
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Determination of Rate Constants for Charge Transfer and the Distribution of Semiconductor and Electrolyte Electronic Energy Levels in Dye-Sensitized Solar Cells by Open-Circuit Photovoltage Decay Method
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Organic Dyes Containing Coplanar Diphenyl-Substituted Dithienosilole Core for Efficient Dye-Sensitized Solar Cells
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Electrochemical Impedance Spectroscopic Analysis of Dye-Sensitized Solar Cells
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Effect of a Coadsorbent on the Performance of Dye-Sensitized TiO 2 Solar Cells: Shielding versus Band-Edge Movement
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Effects of 5-Membered Heteroaromatic Spacers on Structures of Porphyrin Films and Photovoltaic Properties of Porphyrin-Sensitized TiO2 Cells
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Organic Dyes Containing Furan Moiety for High-Performance Dye-Sensitized Solar Cells
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A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films
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Highly-efficient metal-free organic dyes for dye-sensitized solar cells
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Chemical capacitance of nanostructured semiconductors: its origin and significance for nanocomposite solar cells
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A novel organic chromophore for dye-sensitized nanostructured solar cells
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Lighting porphyrins and phthalocyanines for molecular photovoltaics
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Porphyrins and phthalocyanines in solar photovoltaic cells
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inferred← citeshttps://doi.org/10.1021/acs.jpcc.5b04629openalex-snapshot
Tuning the Photovoltaic Performance of Benzocarbazole-Based Sensitizers for Dye-Sensitized Solar Cells: A Joint Experimental and Theoretical Study of the Influence of π-Spacers
inferred← citeshttps://doi.org/10.1021/acsaem.8b00458openalex-snapshot
Tuning the Photovoltaic Performance of DSSCs by Appending Various Donor Groups on trans-Dimesityl Porphyrin Backbone
inferred← citeshttps://doi.org/10.1021/acsami.5b07205openalex-snapshot
2H-[1,2,3]Triazolo[4,5-c]pyridine Cored Organic Dyes Achieving a High Efficiency: a Systematic Study of the Effect of Different Donors and π Spacers
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/acsomega.0c02060openalex-snapshot
Comparison between Benzothiadizole–Thiophene- and Benzothiadizole–Furan-Based D–A−π–A Dyes Applied in Dye-Sensitized Solar Cells: Experimental and Theoretical Insights
inferred← citeshttps://doi.org/10.1021/acsomega.7b01570openalex-snapshot
Synthesis by a Cost-Effective Method and Electroluminescence of a Novel Efficient Yellowish-Green Thermally Activated Delayed Fluorescent Molecule
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c00054openalex-snapshot
Phenylphenothiazine-Based Porous Organic Polymers as Visible-Light Heterogeneous Photocatalysts for Switchable Bromoalkylation and Cyclopropanation of Unactivated Terminal Alkenes
inferred← citeshttps://doi.org/10.1021/am402036jopenalex-snapshot
Facile and Selective Synthesis of Oligothiophene-Based Sensitizer Isomers: An Approach toward Efficient 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/am506149qopenalex-snapshot
Fluorene-Based Sensitizers with a Phenothiazine Donor: Effect of Mode of Donor Tethering on the Performance of Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/cm400800hopenalex-snapshot
Significant Improvement of Dye-Sensitized Solar Cell Performance Using Simple Phenothiazine-Based Dyes
inferred← citeshttps://doi.org/10.1021/jacs.3c05787openalex-snapshot
Super-Reducing Behavior of Benzo[b]phenothiazine Anion Under Visible-Light Photoredox Condition
inferred← citeshttps://doi.org/10.1021/jp4026305openalex-snapshot
Optical Properties and Aggregation of Phenothiazine-Based Dye-Sensitizers for Solar Cells Applications: A Combined Experimental and Computational Investigation
inferred← citeshttps://doi.org/10.1021/jp501017fopenalex-snapshot
Dual Intramolecular Charge-Transfer Fluorescence Derived from a Phenothiazine-Triphenyltriazine Derivative
inferred← citeshttps://doi.org/10.1021/ma3005058openalex-snapshot
Conjugated Polymers of Rylene Diimide and Phenothiazine for n-Channel Organic Field-Effect Transistors
inferred← citeshttps://doi.org/10.1021/ol4001685openalex-snapshot
Cyclic Thiourea/Urea Functionalized Triphenylamine-Based Dyes for High-Performance Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1038/srep46268openalex-snapshot
Crystallisation-enhanced bulk hole mobility in phenothiazine-based organic semiconductors
inferred← citeshttps://doi.org/10.1039/c2cp40872dopenalex-snapshot
Synthesis and photovoltaic properties of organic sensitizers incorporating a thieno[3,4-c]pyrrole-4,6-dione moiety
inferred← citeshttps://doi.org/10.1039/c2jm32333hopenalex-snapshot
Novel branched coumarin dyes for dye-sensitized solar cells: significant improvement in photovoltaic performance by simple structure modification
inferred← citeshttps://doi.org/10.1039/c2jm35556fopenalex-snapshot
Organic dyes containing oligo-phenothiazine for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c2nj40374aopenalex-snapshot
Synthesis and applications of new triphenylamine dyes with donor–donor–(bridge)–acceptor structure for organic dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c3cs35372aopenalex-snapshot
Arylamine organic dyes for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c3ra22249gopenalex-snapshot
Structural variations of D–π–A dyes influence on the photovoltaic performance of dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c4cc09294eopenalex-snapshot
Eugenic metal-free sensitizers with double anchors for high performance dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c4nj00428kopenalex-snapshot
Electronic tuning effects via π-linkers in tetrathiafulvalene-based dyes
inferred← citeshttps://doi.org/10.1039/c4ra05584eopenalex-snapshot
A novel carbazole–phenothiazine dyad small molecule as a non-fullerene electron acceptor for polymer bulk heterojunction solar cells
inferred← citeshttps://doi.org/10.1039/c4ra07967aopenalex-snapshot
Approach to tune short-circuit current and open-circuit voltage of dye-sensitized solar cells: π-linker modification and photoanode selection
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/c4ra11264dopenalex-snapshot
Fundamental aspects of property tuning in push–pull molecules
inferred← citeshttps://doi.org/10.1039/c4ta02639jopenalex-snapshot
Dithienopyrrolobenzothiadiazole-based organic dyes for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c4ta02720eopenalex-snapshot
Spacer effects in metal-free organic dyes for visible-light-driven dye-sensitized photocatalytic hydrogen production
inferred← citeshttps://doi.org/10.1039/c5nj02967hopenalex-snapshot
Enhanced performance of dye-sensitized solar cells with Y-shaped organic dyes containing di-anchoring groups
inferred← citeshttps://doi.org/10.1039/c5ra07785kopenalex-snapshot
Molecular design of new organic sensitizers based on thieno[1,4]benzothiazine for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c5sc02778kopenalex-snapshot
Unprecedentedly targeted customization of molecular energy levels with auxiliary-groups in organic solar cell sensitizers
inferred← citeshttps://doi.org/10.1039/c5ta01025jopenalex-snapshot
Enhanced performance of quasi-solid-state dye-sensitized solar cells by tuning the building blocks in D–(π)–A′–π–A featured organic dyes
inferred← citeshttps://doi.org/10.1039/c5tc01423aopenalex-snapshot
Rational design of phenothiazine (PTz) and ethylenedioxythiophene (EDOT) based donor–acceptor compounds with a molecular aggregation breaker for solid state emission in red and NIR regions
inferred← citeshttps://doi.org/10.1039/c5tc02014jopenalex-snapshot
Triggering DRAM/SRAM memory behaviors by single atom substitution to alter the molecular planarity
inferred← citeshttps://doi.org/10.1039/c5tc03308jopenalex-snapshot
Molecular engineering of starburst triarylamine donor with selenophene containing π-linker for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c5tc04418aopenalex-snapshot
Phenothiazine-based dyes for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c6nj02040bopenalex-snapshot
Can fused-pyrrole rings act as better π-spacer units than fused-thiophene in dye-sensitized solar cells? A computational study
inferred← citeshttps://doi.org/10.1039/c6qm00271dopenalex-snapshot
Improvement of D–π–A organic dye-based dye-sensitized solar cell performance by simple triphenylamine donor substitutions on the π-linker of the dye
inferred← citeshttps://doi.org/10.1039/c6tc01269hopenalex-snapshot
Improving the electroluminescence performance of donor–acceptor molecules by fine-tuning the torsion angle and distance between donor and acceptor moieties
inferred← citeshttps://doi.org/10.1039/c7nj02181jopenalex-snapshot
Double-anchoring organic dyes for dye-sensitized solar cells: the opto-electronic property and performance
inferred← citeshttps://doi.org/10.1039/c7ta01744hopenalex-snapshot
Novel ethynyl-pyrene substituted phenothiazine based metal free organic dyes in DSSC with 12% conversion efficiency
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/c8ra04450copenalex-snapshot
Efficiency difference between furan- and thiophene-based D–π–A dyes in DSSCs explained by theoretical calculations
inferred← citeshttps://doi.org/10.1039/c9nj01720hopenalex-snapshot
Effect of furan π-spacer and triethylene oxide methyl ether substituents on performance of phenothiazine sensitizers in dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/c9ta00472fopenalex-snapshot
Auxiliary donors for phenothiazine sensitizers for dye-sensitized solar cells – how important are they really?
inferred← citeshttps://doi.org/10.1039/d0cp01664kopenalex-snapshot
Theoretical analysis of the absorption spectrum, electronic structure, excitation, and intramolecular electron transfer of D–A′–π–A porphyrin dyes for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1039/d1ma00499aopenalex-snapshot
Indole fused heterocycles as sensitizers in dye-sensitized solar cells: an overview
inferred← citeshttps://doi.org/10.1039/d1tc03207kopenalex-snapshot
Phenothiazine and phenoxazine sensitizers for dye-sensitized solar cells – an investigative review of two complete dye classes
inferred← citeshttps://doi.org/10.1039/d3cp03664bopenalex-snapshot
Study of the microscopic mechanism of stepwise charge injection in co-sensitive DSSCs in the framework of a D–π–A dye and chlorophyll
inferred← citeshttps://doi.org/10.1039/d5ta00518copenalex-snapshot
The competitive influence of the intramolecular electric field and hydrophilic active sites of D–A conjugated porous polymers on photocatalytic hydrogen evolution performance
inferred← citeshttps://doi.org/10.1039/d5tc01000dopenalex-snapshot
Carbazole–phenothiazine-based organic sensitizers via π-bridge functionalization with different electronegative/steric substituents: photophysical properties and DSSC performance
inferred← citeshttps://doi.org/10.1088/0957-4484/27/26/265701openalex-snapshot
Screening π -conjugated bridges of organic dyes for dye-sensitized solar cells with panchromatic visible light harvesting
inferred← citeshttps://doi.org/10.1107/s160053681200462xopenalex-snapshot
10-Ethyl-3-(5-methyl-1,3,4-oxadiazol-2-yl)-10H-phenothiazine
inferred← citeshttps://doi.org/10.1107/s160053681201361xopenalex-snapshot
2-(5-Bromothiophen-2-yl)-5-[5-(10-ethylphenothiazin-3-yl)thiophen-2-yl]-1,3,4-oxadiazole
inferred← citeshttps://doi.org/10.1107/s2056989017005540openalex-snapshot
Crystal structure of 10-ethyl-7-(9-ethyl-9H-carbazol-3-yl)-10H-phenothiazine-3-carbaldehyde
inferred← citeshttps://doi.org/10.1108/prt-08-2022-0094openalex-snapshot
Phenothiazine- isophorone dyes (D–π–A and A–π–D–π–A): synthesis, electronic properties and DFT computational study
inferred← citeshttps://doi.org/10.1115/1.4028005openalex-snapshot
Nanoparticles of Cadmium Nitrate and Cobalt Nitrate Complexes Bearing Phosphoramide Ligands Designed for Application in Dye Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1134/s0036024423110298openalex-snapshot
Design and Synthesis of Phenylacridine-Based on Organic Dyes and Its Applications in Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1142/s108842461650098xopenalex-snapshot
Broad-absorbing tetrabenzocorrolazine green photosensitizer for the enhanced conversion efficiency in dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1186/s11671-018-2760-6openalex-snapshot
Dye-Sensitized Solar Cells: Fundamentals and Current Status
inferred← citeshttps://doi.org/10.1246/cl.130931openalex-snapshot
Dye-sensitized Solar Cells Based on 1,3-Dithiol-2-ylidene Derivatives: Substituent and π-Spacer Effects on the Efficiency
inferred← citeshttps://doi.org/10.14233/ajchem.2021.23340openalex-snapshot
Fused Thiazine Tethered Metal-Free Dyes for Dye Sensitized Solar Cells: A Computational Investigation
inferred← citeshttps://doi.org/10.21203/rs.3.rs-886812/v1openalex-snapshot
Synthesis, Photophysical, Electrochemical, and DFT Examinations of Two New Organic Dye Molecules Based on Phenothiazine and Dibenzofuran
inferred← citeshttps://doi.org/10.2174/1385272824666200311151421openalex-snapshot
Organic Triads for Solar Cells Application: A Review
inferred← citeshttps://doi.org/10.3184/174751917x14967701767049openalex-snapshot
Synthesis of new derivatives of 4-(4-methyl-5 H -pyrimido[4,5- b ][1,4]thiazin-2-yl)morpholine and 4-methyl-2-(piperidin-1-yl)-5 H -pyrimido[4,5- b ][1,4]thiazine
inferred← citeshttps://doi.org/10.3390/ma12010193openalex-snapshot
Design, Electron Transfer Process, and Opto-Electronic Property of Solar Cell Using Triphenylamine-Based D-π-A Architectures
inferred← citeshttps://doi.org/10.4236/msce.2018.67004openalex-snapshot
Performance Improvement of Dye-Sensitized Solar Cell by Phenanthrothiadiazole Unit-Based π-Conjugated Bridge
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