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Insight into D–A−π–A Structured Sensitizers: A Promising Route to Highly Efficient and Stable Dye-Sensitized Solar Cells
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Organic D‐A‐π‐A Solar Cell Sensitizers with Improved Stability and Spectral Response
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Significant Improvement of Dye‐Sensitized Solar Cell Performance by Small Structural Modification in π‐Conjugated Donor–Acceptor Dyes
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Stability of Polymer Solar Cells
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Hexylthiophene‐Featured D–A–π–A Structural Indoline Chromophores for Coadsorbent‐Free and Panchromatic Dye‐Sensitized Solar Cells
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Metal‐Free Organic Dyes for Dye‐Sensitized Solar Cells: From Structure: Property Relationships to Design Rules
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Highly Efficient Mesoscopic Dye‐Sensitized Solar Cells Based on Donor–Acceptor‐Substituted Porphyrins
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Highly Efficient Dye‐Sensitized Solar Cells Based on Panchromatic Ruthenium Sensitizers with Quinolinylbipyridine Anchors
inferredcites →https://doi.org/10.1002/anie.201309343openalex-snapshot
Molecular Engineering of Push–Pull Porphyrin Dyes for Highly Efficient Dye‐Sensitized Solar Cells: The Role of Benzene Spacers
inferredcites →https://doi.org/10.1002/anie.201406190openalex-snapshot
Efficient Solar Cells Sensitized by Porphyrins with an Extended Conjugation Framework and a Carbazole Donor: From Molecular Design to Cosensitization
inferredcites →https://doi.org/10.1002/asia.201100967openalex-snapshot
Benzotriazole‐Bridged Sensitizers Containing a Furan Moiety for Dye‐Sensitized Solar Cells with High Open‐Circuit Voltage Performance
inferredcites →https://doi.org/10.1002/asia.201200648openalex-snapshot
Tuning the Electrical and Optical Properties of Diketopyrrolopyrrole Complexes for Panchromatic Dye‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1002/asia.201201173openalex-snapshot
Benzotriazole‐Containing D–π–A Conjugated Organic Dyes for Dye‐Sensitized Solar Cells
inferredcites →https://doi.org/10.1002/chem.201103542openalex-snapshot
Constructing Organic D–A–π‐A‐Featured Sensitizers with a Quinoxaline Unit for High‐Efficiency Solar Cells: The Effect of an Auxiliary Acceptor on the Absorption and the Energy Level Alignment
inferredcites →https://doi.org/10.1002/ejoc.201201424openalex-snapshot
5,6‐Bis(octyloxy)benzo[c][1,2,5]thiadiazole‐Bridged Dyes for Dye‐Sensitized Solar Cells with High Open‐Circuit Voltage Performance
inferredcites →https://doi.org/10.1002/qua.24611openalex-snapshot
Molecular design of organic dyes with diketopyrrolopyrrole for dye‐sensitized solar cell: A theoretical approach
inferredcites →https://doi.org/10.1007/s11426-012-4517-xopenalex-snapshot
New D-π-A dyes for efficient dye-sensitized solar cells
inferredcites →https://doi.org/10.1016/j.dyepig.2012.02.015openalex-snapshot
Novel D–A–π–A coumarin dyes containing low band-gap chromophores for dye-sensitised solar cells
inferredcites →https://doi.org/10.1016/j.dyepig.2012.05.020openalex-snapshot
How to design proper π-spacer order of the D-π-A dyes for DSSCs? A density functional response
inferredcites →https://doi.org/10.1016/j.dyepig.2013.02.008openalex-snapshot
Density functional theory characterization and verification of high-performance indoline dyes with D–A–π–A architecture for dye-sensitized solar cells
inferredcites →https://doi.org/10.1016/j.dyepig.2013.04.031openalex-snapshot
Organic sensitizers incorporating 3,4-ethylenedioxythiophene as the conjugated bridge: Joint photophysical and electrochemical analysis of photovoltaic performance
inferredcites →https://doi.org/10.1016/j.dyepig.2014.08.005openalex-snapshot
Structure–property relationships: Steric effect in ancillary ligand and how it influences photocurrent and photovoltage in dye-sensitized solar cells
inferredcites →https://doi.org/10.1016/j.jpowsour.2013.08.034openalex-snapshot
Effects of the acceptors in triphenylamine-based D–A′–π–A dyes on photophysical, electrochemical, and photovoltaic properties
inferredcites →https://doi.org/10.1016/j.jpowsour.2014.11.107openalex-snapshot
Probing the regeneration process of triphenylamine-based organic dyes in dye-sensitized solar cells
inferredcites →https://doi.org/10.1016/j.mattod.2013.01.020openalex-snapshot
Recent trends in mesoscopic solar cells based on molecular and nanopigment light harvesters
inferredcites →https://doi.org/10.1016/j.saa.2014.07.094openalex-snapshot
DFT and TD-DFT study on geometries, electronic structures and electronic absorption of some metal free dye sensitizers for dye sensitized solar cells
inferredcites →https://doi.org/10.1016/s1389-5567(03)00026-1openalex-snapshot
Dye-sensitized solar cells
inferredcites →https://doi.org/10.1021/am3001049openalex-snapshot
D-A-π-A Featured Sensitizers Bearing Phthalimide and Benzotriazole as Auxiliary Acceptor: Effect on Absorption and Charge Recombination Dynamics in Dye-Sensitized Solar Cells
inferredcites →https://doi.org/10.1021/am300925eopenalex-snapshot
Series of New D-A-π-A Organic Broadly Absorbing Sensitizers Containing Isoindigo Unit for Highly Efficient Dye-Sensitized Solar Cells
inferredcites →https://doi.org/10.1021/am400754dopenalex-snapshot
Constructing High-Efficiency D–A−π–A-Featured Solar Cell Sensitizers: a Promising Building Block of 2,3-Diphenylquinoxaline for Antiaggregation and Photostability
inferredcites →https://doi.org/10.1021/am503891qopenalex-snapshot
Effect of a Long Alkyl Group on Cyclopentadithiophene as a Conjugated Bridge for D–A−π–A Organic Sensitizers: IPCE, Electron Diffusion Length, and Charge Recombination
inferredcites →https://doi.org/10.1021/am507261jopenalex-snapshot
Efficient Triarylamine–Perylene Dye-Sensitized Solar Cells: Influence of Triple-Bond Insertion on Charge Recombination
inferredcites →https://doi.org/10.1021/am508623eopenalex-snapshot
Cosensitization of D-A-π-A Quinoxaline Organic Dye: Efficiently Filling the Absorption Valley with High Photovoltaic Efficiency
inferredcites →https://doi.org/10.1021/ar2002446openalex-snapshot
Molecular Design of Photovoltaic Materials for Polymer Solar Cells: Toward Suitable Electronic Energy Levels and Broad Absorption
inferredcites →https://doi.org/10.1021/cm202226jopenalex-snapshot
Incorporating Benzotriazole Moiety to Construct D–A−π–A Organic Sensitizers for Solar Cells: Significant Enhancement of Open-Circuit Photovoltage with Long Alkyl Group
inferredcites →https://doi.org/10.1021/ja003299uopenalex-snapshot
Engineering of Efficient Panchromatic Sensitizers for Nanocrystalline TiO 2 -Based Solar Cells
inferredcites →https://doi.org/10.1021/ja052467lopenalex-snapshot
Combined Experimental and DFT-TDDFT Computational Study of Photoelectrochemical Cell Ruthenium Sensitizers
inferredcites →https://doi.org/10.1021/ja0771989openalex-snapshot
Toward a Rational Design of Poly(2,7-Carbazole) Derivatives for Solar Cells
inferredcites →https://doi.org/10.1021/ja207978vopenalex-snapshot
It Takes More Than an Imine: The Role of the Central Atom on the Electron-Accepting Ability of Benzotriazole and Benzothiadiazole Oligomers
inferredcites →https://doi.org/10.1021/ja500280ropenalex-snapshot
Influence of the Donor Size in D−π–A Organic Dyes for Dye-Sensitized Solar Cells
inferredcites →https://doi.org/10.1021/jacs.5b01537openalex-snapshot
Donor/Acceptor Indenoperylene Dye for Highly Efficient Organic Dye-Sensitized Solar Cells
inferredcites →https://doi.org/10.1021/jp402645hopenalex-snapshot
Molecular Engineering of Indoline-Based D–A−π–A Organic Sensitizers toward High Efficiency Performance from First-Principles Calculations
inferredcites →https://doi.org/10.1021/jp411504popenalex-snapshot
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
inferredcites →https://doi.org/10.1021/jp412259topenalex-snapshot
Dye-Sensitized Solar Cells Based on Quinoxaline Dyes: Effect of π-Linker on Absorption, Energy Levels, and Photovoltaic Performances
inferredcites →https://doi.org/10.1021/jp909786kopenalex-snapshot
New Diketopyrrolopyrrole (DPP) Dyes for Efficient Dye-Sensitized Solar Cells
inferredcites →https://doi.org/10.1021/ol2012378openalex-snapshot
Novel Quinoxaline-Based Organic Sensitizers for Dye-Sensitized Solar Cells
inferredcites →https://doi.org/10.1021/ol501163bopenalex-snapshot
Incorporating a New 2H-[1,2,3]Triazolo[4,5-c]pyridine Moiety To Construct D–A−π–A Organic Sensitizers for High Performance Solar Cells
inferredcites →https://doi.org/10.1021/sc500035jopenalex-snapshot
Insight into Benzothiadiazole Acceptor in D–A−π–A Configuration on Photovoltaic Performances of Dye-Sensitized Solar Cells
inferredcites →https://doi.org/10.1038/353737a0openalex-snapshot
A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films
inferredcites →https://doi.org/10.1038/nature11476openalex-snapshot
Materials interface engineering for solution-processed photovoltaics
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/10.1038/nphoton.2013.136openalex-snapshot
Wideband dye-sensitized solar cells employing a phosphine-coordinated ruthenium sensitizer
inferredcites →https://doi.org/10.1038/srep02446openalex-snapshot
Blue-Coloured Highly Efficient Dye-Sensitized Solar Cells by Implementing the Diketopyrrolopyrrole Chromophore
inferredcites →https://doi.org/10.1038/srep04033openalex-snapshot
A Robust Organic Dye for Dye Sensitized Solar Cells Based on Iodine/Iodide Electrolytes Combining High Efficiency and Outstanding Stability
inferredcites →https://doi.org/10.1039/b820964bopenalex-snapshot
Conveniently synthesized isophorone dyes for high efficiency dye-sensitized solar cells: tuning photovoltaic performance by structural modification of donor group in donor–π–acceptor system
inferredcites →https://doi.org/10.1039/b900372jopenalex-snapshot
Highly stable sensitizer dyes for dye-sensitized solar cells: role of the oligothiophene moiety
inferredcites →https://doi.org/10.1039/c003841eopenalex-snapshot
Improvement of dye-sensitized solar cells: what we know and what we need to know
inferredcites →https://doi.org/10.1039/c0ee00788aopenalex-snapshot
Absorption and photovoltaic properties of organic solar cell sensitizers containing fluorene unit as conjunction bridge
inferredcites →https://doi.org/10.1039/c2cc17886aopenalex-snapshot
Diketopyrrolopyrrole (DPP)-based materials for organic photovoltaics
inferredcites →https://doi.org/10.1039/c2cc31998eopenalex-snapshot
A novel D–A-π-A organic sensitizer containing a diketopyrrolopyrrole unit with a branched alkyl chain for highly efficient and stable dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c2cc35125kopenalex-snapshot
A structural study of DPP-based sensitizers for DSC applications
inferredcites →https://doi.org/10.1039/c2cc35597copenalex-snapshot
Towards high-performance DPP-based sensitizers for DSC applications
inferredcites →https://doi.org/10.1039/c2cs35346fopenalex-snapshot
Organic sensitizers from D–π–A to D–A–π–A: effect of the internal electron-withdrawing units on molecular absorption, energy levels and photovoltaic performances
inferredcites →https://doi.org/10.1039/c2ee03418bopenalex-snapshot
High-efficiency dye-sensitized solar cell with a novel co-adsorbent
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
inferredcites →https://doi.org/10.1039/c2jm30362kopenalex-snapshot
Recent developments in molecule-based organic materials for dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c2jm33105eopenalex-snapshot
Incorporating a stable fluorenone unit into D–A–π–A organic dyes for dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c2jm33833eopenalex-snapshot
High performance organic sensitizers based on 11,12-bis(hexyloxy) dibenzo[a,c]phenazine for dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c3cc00060eopenalex-snapshot
New donor–π–acceptor sensitizers containing 5H-[1,2,5]thiadiazolo [3,4-f]isoindole-5,7(6H)-dione and 6H-pyrrolo[3,4-g]quinoxaline-6,8(7H)-dione units
inferredcites →https://doi.org/10.1039/c3ta10618gopenalex-snapshot
A novel compact DPP dye with enhanced light harvesting and charge transfer properties for highly efficient DSCs
inferredcites →https://doi.org/10.1039/c3ta13643dopenalex-snapshot
Diketopyrrolopyrrole-based sensitizers for dye-sensitized solar cell applications: anchor engineering
inferredcites →https://doi.org/10.1039/c4cc00577eopenalex-snapshot
A benzothiazole–cyclopentadithiophene bridged D–A–π–A sensitizer with enhanced light absorption for high efficiency dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c4cc00783bopenalex-snapshot
Molecular engineering of panchromatic isoindigo sensitizers for dye-sensitized solar cell applications
inferredcites →https://doi.org/10.1039/c4cs00152dopenalex-snapshot
Stability enhancement of fluorophores for lighting up practical application in bioimaging
inferredcites →https://doi.org/10.1039/c4dt02756fopenalex-snapshot
Porphyrins as excellent dyes for dye-sensitized solar cells: recent developments and insights
inferredcites →https://doi.org/10.1039/c4ra01858copenalex-snapshot
Phenothiazine derivatives-based D–π–A and D–A–π–A organic dyes for dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c4ta02111hopenalex-snapshot
Deposition of loosely bound organic D–A–π–A′ dyes on sensitized TiO 2 film: a possible strategy to suppress charge recombination and enhance power conversion efficiency in dye-sensitized solar cells
inferredcites →https://doi.org/10.1039/c4ta05350hopenalex-snapshot
Effects of various π-conjugated spacers in thiadiazole[3,4-c]pyridine-cored panchromatic organic dyes for dye-sensitized solar cells
inferredcites →https://doi.org/10.1126/science.1209688openalex-snapshot
Porphyrin-Sensitized Solar Cells with Cobalt (II/III)–Based Redox Electrolyte Exceed 12 Percent Efficiency
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Tuning the photophysical properties of triphenylamine pyrazine-based dyes: role of π-spacers in DSSCs with iodine and copper-based redox shuttle
inferred← citeshttps://doi.org/10.1007/s10008-022-05119-9openalex-snapshot
Novel metal complexes of pyridineimine derivative used as auxiliary electron acceptor of D-(A-π-A)2 motif dye sensitizer: synthesis and photovoltaic application
inferred← citeshttps://doi.org/10.1007/s10853-023-08376-9openalex-snapshot
Calcium-doped TiO2 microspheres and near-infrared carbazole-based sensitizer for efficient co-sensitized dye-sensitized solar cell
inferred← citeshttps://doi.org/10.1007/s10854-017-6594-2openalex-snapshot
Effects of donor position on dibenzofulvene-based organic dyes for photovoltaics
inferred← citeshttps://doi.org/10.1007/s10854-017-7787-4openalex-snapshot
Effect of electron-deficient linkers on the physical and photovoltaic properties of dithienopyrrole-based organic dyes
inferred← citeshttps://doi.org/10.1007/s10876-026-03009-yopenalex-snapshot
Enhancing DSSC Performance Via Comparative Design of D–A–π–A and D–D–π–A Organic Dyes: DFT Calculations of Structure–property Correlation
inferred← citeshttps://doi.org/10.1007/s10895-025-04404-wopenalex-snapshot
Impact of π-Extended Auxiliary Acceptors on the Photovoltaic Performance of Dithienosilole-Based Sensitizers. A DFT/TDDFT Investigation
inferred← citeshttps://doi.org/10.1007/s10904-021-02220-wopenalex-snapshot
Novel Polymeric Metal Complexes for Dye Sensitizer: Synthesis and Photovoltaic Performances
inferred← citeshttps://doi.org/10.1007/s11164-016-2803-5openalex-snapshot
Synthesis and photoelectric property of N-confused porphyrins bearing an ethynylbenzoic and benzoic acid moiety
inferred← citeshttps://doi.org/10.1007/s11172-024-4341-4openalex-snapshot
Dye-sensitized solar cells based on D—A—π—A′ structures with a 4H-cyclopenta[2,1-b:3,4-b′]dithiophene fragment containing branched alkyl groups
inferred← citeshttps://doi.org/10.1007/s11664-019-07228-0openalex-snapshot
Molecular Design of D-π-A-A Organic Dyes Based on Triphenylamine Derivatives with Various Auxiliary Acceptors for High Performance DSSCs
inferred← citeshttps://doi.org/10.1007/s11664-019-07777-4openalex-snapshot
Theoretical Study on Factors Influencing the Efficiency of D–π′–A′–π–A Isoindigo-Based Sensitizer for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1007/s12034-020-02198-0openalex-snapshot
Design and synthesis of organic dyes with various donor groups: promising dyes for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1007/s12200-016-0563-xopenalex-snapshot
Donor design and modification strategies of metal-free sensitizers for highly-efficient n-type dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1007/s12200-016-0567-6openalex-snapshot
Effect of electron-withdrawing groups in conjugated bridges: molecular engineering of organic sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1007/s13762-024-06065-xopenalex-snapshot
Porphyrinoid macrocycles as potential photosensitizers for photodynamic inhibition of biofilm formation in household water storage systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-815647-6.00001-7openalex-snapshot
Introduction and Importance of Synthetic Organic Dyes
inferred← citeshttps://doi.org/10.1016/j.apcatb.2016.06.061openalex-snapshot
Bottom-up construction of highly photoactive dye-sensitized titania using Ru(II) and Ir(III) complexes as building blocks
inferred← citeshttps://doi.org/10.1016/j.apsusc.2017.06.329openalex-snapshot
Superhydrophobicity construction with dye-sensitised TiO 2 on fabric surface for both oil/water separation and water bulk contaminants purification
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.04.007openalex-snapshot
Transition metal-catalyzed cross-coupling methodologies for the engineering of small molecules with applications in organic electronics and photovoltaics
inferred← citeshttps://doi.org/10.1016/j.ccr.2024.216143openalex-snapshot
Recent advances in metal-free photosensitizers for dye-sensitized photoelectrochemical cells
inferred← citeshttps://doi.org/10.1016/j.chemphys.2022.111738openalex-snapshot
Carbazole based D-πi-π-A dyes for DSSC applications: DFT/TDDFT study of the influence of πi-spacers on the photovoltaic performance
inferred← citeshttps://doi.org/10.1016/j.chemphys.2024.112562openalex-snapshot
Theoretical study of the photovoltaic properties of dye-sensitized solar cells with novel D-A-π-A-type benzothiazole molecules as auxiliary acceptors
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2016.08.083openalex-snapshot
Interfacial self-assembly, characterization, electrochemical, and photo-catalytic properties of porphyrin-ruthenium complex/polyoxomelate triad hybrid multilayers
inferred← citeshttps://doi.org/10.1016/j.colsurfa.2022.128500openalex-snapshot
Pyridine enhances the efficiency of 1D-CdS nanowire solar cells fabricated using novel organic dyes
inferred← citeshttps://doi.org/10.1016/j.comptc.2018.09.003openalex-snapshot
Tuning of some novel triphenylamine-based organic dyes for their potential application in dye-sensitized solar cells: A theoretical study
inferred← citeshttps://doi.org/10.1016/j.dyepig.2016.04.020openalex-snapshot
Molecular engineering of largely π-extended metal-free sensitizers containing benzothiadiazole units: Approaching 10% efficiency dye-sensitized solar cells using iodine-based electrolytes
inferred← citeshttps://doi.org/10.1016/j.dyepig.2016.10.006openalex-snapshot
Synthesis and photovoltaic performance of the porphyrin based sensitizers with 2H-[1,2,3]triazolo[4,5-c]pyridine and benzotriazole as auxiliary acceptors
inferred← citeshttps://doi.org/10.1016/j.dyepig.2016.10.041openalex-snapshot
Branched and linear alkoxy chains-wrapped push-pull porphyrins for developing efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2016.12.027openalex-snapshot
Influence of the additional electron-withdrawing unit in β-functionalized porphyrin sensitizers on the photovoltaic performance of dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2016.12.053openalex-snapshot
Dye sensitizers of polymer using the complex of Cd (II) or Cu (II) with imidazole as auxiliary electron acceptor for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2017.02.013openalex-snapshot
New benzoselenadiazole-based D–A–π–A type triarylamine sensitizers for highly efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2017.02.017openalex-snapshot
Effects of donors of bodipy dyes on the performance of dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2017.06.068openalex-snapshot
The impact of adjusting auxiliary donors on the performance of dye-sensitized solar cells based on phenothiazine D-D-π-A sensitizers
inferred← citeshttps://doi.org/10.1016/j.dyepig.2017.08.055openalex-snapshot
Synthesis and properties of new benzothiadiazole-based push-pull dyes for p-type dye sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2017.09.055openalex-snapshot
Incorporating quinoxaline unit as additional acceptor for constructing efficient donor-free solar cell sensitizers
inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.05.044openalex-snapshot
Tailoring the benzotriazole (BTZ) auxiliary acceptor in a D-A′-π-A type sensitizer for high performance dye-sensitized solar cells (DSSCs)
inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.05.060openalex-snapshot
Molecular engineering of ruthenium-diacetylide organometallic complexes towards efficient green dye for DSSC
inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.08.029openalex-snapshot
Trans-A2B2 Zn(II) porphyrin dyes with various donor groups and their Co-sensitization for highly efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.12.042openalex-snapshot
New 2,3-diphenylquinoxaline containing organic D-A-π-A dyes with nickel oxide photocathode prepared by surfactant-mediated synthesis for high performance p-type dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.02.013openalex-snapshot
Triazine-branched mono- and dianchoring organic dyes: Effect of acceptor arms on optical and photovoltaic properties
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.107954openalex-snapshot
Dopant-free benzothiadiazole bridged hole transport materials for highly stable and efficient perovskite solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.107984openalex-snapshot
Porphyrin sensitizers involving a fluorine-substituted benzothiadiazole as auxiliary acceptor and thiophene as π bridge for use in dye-sensitized solar cells (DSSCs)
inferred← citeshttps://doi.org/10.1016/j.dyepig.2019.108036openalex-snapshot
The planarization of side chain in carbazole sensitizer and its effect on optical, electrochemical, and interfacial charge transfer properties
inferred← citeshttps://doi.org/10.1016/j.dyepig.2020.109074openalex-snapshot
Donor group influence on dye-sensitized solar cell device performances: Balancing dye loading and donor size
inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109220openalex-snapshot
Influence of various dithienoheterocycles as conjugated linker in Naphtho[2,3-d] [1,2,3]triazole-based organic dyes for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109447openalex-snapshot
Antagonistic activity of hydroxycoumarin-based antioxidants as possible singlet oxygen precursor photosensitizers
inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109582openalex-snapshot
Effect of substituents of phenyl of π-linkage in carbazole sensitizers on the photovoltaic performance of the dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109638openalex-snapshot
Advances in phenothiazine and phenoxazine-based electron donors for organic dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109667openalex-snapshot
New benzotriazole-based D–A–D type solvatochromic dyes for water content detection in organic solvents
inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109922openalex-snapshot
Molecular engineering of the fused azacycle donors in the D-A-π-A metal-free organic dyes for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110566openalex-snapshot
Pyranylidene/trifluoromethylbenzoic acid-based chromophores for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110615openalex-snapshot
A strategy for efficient parallel tandem dye-sensitized solar cells based on doubled-sided Pt electrode with a novel phenothiazine-based dye and N719
inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110771openalex-snapshot
Novel polymeric metal complexes of pyridine derivatives for being used as dye sensitizers
inferred← citeshttps://doi.org/10.1016/j.dyepig.2023.111322openalex-snapshot
Molecular engineering of auxiliary acceptor for the development of efficient organic D-A-π-A sensitizers
inferred← citeshttps://doi.org/10.1016/j.dyepig.2024.112018openalex-snapshot
A novel AIE-based imidazolium for carbonate ion detection
inferred← citeshttps://doi.org/10.1016/j.electacta.2019.02.013openalex-snapshot
Phenothiazine dye featuring encapsulated insulated molecular wire as auxiliary donor for high photovoltage of dye-sensitized solar cells by suppression of aggregation
inferred← citeshttps://doi.org/10.1016/j.enchem.2019.100015openalex-snapshot
Recent advances in dye-sensitized photoelectrochemical cells for water splitting
inferred← citeshttps://doi.org/10.1016/j.gce.2022.07.005openalex-snapshot
D-A-π-A organic dyes with fluorenyl-substituted bulky donor for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.gee.2016.02.001openalex-snapshot
WITHDRAWN: Cosensitization process effect of D-A-π-A featured dyes on photovoltaic performances
inferred← citeshttps://doi.org/10.1016/j.gee.2016.04.003openalex-snapshot
Cosensitization process effect of D-A-π-A featured dyes on photovoltaic performances
inferred← citeshttps://doi.org/10.1016/j.gee.2016.12.001openalex-snapshot
Amazing long-lived lifetime
inferred← citeshttps://doi.org/10.1016/j.ijleo.2020.165030openalex-snapshot
A DFT study of influence of dichloromethane solvent and electric field on light absorption and electronic properties of two Quinoxaline-based solar cells
inferred← citeshttps://doi.org/10.1016/j.jallcom.2023.172000openalex-snapshot
A concise review of recent advances in carbon nitride-based intramolecular donor–acceptor architectures for photocatalytic hydrogen production: Heteromolecular coupling of organic compounds
inferred← citeshttps://doi.org/10.1016/j.jelechem.2015.05.028openalex-snapshot
The effect of the different donor units on fluorescent conjugated polymers containing 2,1,3-benzooxadiazole as the acceptor unit
inferred← citeshttps://doi.org/10.1016/j.jlumin.2018.09.001openalex-snapshot
Synthesis, luminescence and excited state absorption properties of conjugated D-π-A and D-π-D phenothiazine compounds
inferred← citeshttps://doi.org/10.1016/j.jmgm.2023.108512openalex-snapshot
The impact of aromatic π-spacers and internal acceptors in triphenylamine dyes for DSSCs: A DFT approach
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2016.05.015openalex-snapshot
Incorporation of a fluorophenylene spacer into a highly efficient organic dye for solid-state dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2016.08.033openalex-snapshot
Influence of the auxiliary acceptor and π-bridge in carbazole dyes on photovoltaic properties
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2016.10.006openalex-snapshot
Electronic effects on a D-π-A organic sensitizer upon heteroatom substitutions in the π-bridge
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2019.02.015openalex-snapshot
The solvatochromism and aggregation-induce enhanced emission of triphenylamine substituted styrene derivatives and its application in dye sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2019.112333openalex-snapshot
9-(p-Tolyl)-2,3,4,4a,9,9a-hexahydro-1H-carbazole—A new donor building-block in the design of sensitizers for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2020.112936openalex-snapshot
The improvement of photovoltaic performance of quinoline-based dye-sensitized solar cells by modification of the auxiliary acceptors
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2021.113738openalex-snapshot
Impact of internal (donor/acceptor) moieties and π-spacer in triphenylamine-based dyes for DSSCs
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2025.116368openalex-snapshot
New carbazole-based symmetric double D–A type chromophores for DSSC application: Impact of di-anchoring nature on photoelectrochemical processes
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2025.116874openalex-snapshot
D-A-D based NIR and visible homodimeric squaraine dyes for dye-sensitized solar cells: Modulation of excitonic coupling
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2026.117320openalex-snapshot
Derivative design from a high-performance dye: A theoretical investigation on ZS12-based sensitizers with modified π-spacers
inferred← citeshttps://doi.org/10.1016/j.jphotochem.2026.117639openalex-snapshot
DFT/TDDFT study on auxiliary acceptor engineering of D–A1–π1–A2–π2–A3 organic dyes for high-performance dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2015.10.111openalex-snapshot
Nitrogen-doped carbon onions encapsulating metal alloys as efficient and stable catalysts for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2016.09.141openalex-snapshot
New benzothiadiazole-based dyes incorporating dithieno[3,2-b:2′,3′-d]pyrrole (DTP) π-linker for dye-sensitized solar cells with different electrolytes
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2016.09.149openalex-snapshot
Studies on D-A-π-A structured porphyrin sensitizers with different additional electron-withdrawing unit
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2017.01.115openalex-snapshot
Novel D-π-A-π-A coumarin dyes for highly efficient dye-sensitized solar cells: Effect of π-bridge on optical, electrochemical, and photovoltaic performance
inferred← citeshttps://doi.org/10.1016/j.jpowsour.2018.03.059openalex-snapshot
The improved photovoltaic performance of phenothiazine-dithienopyrrole based dyes with auxiliary acceptors
inferred← citeshttps://doi.org/10.1016/j.matlet.2018.05.127openalex-snapshot
Nanocomposites of carbon allotropes with TiO2 as effective photoanodes for efficient dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.molliq.2020.112594openalex-snapshot
Effect of charge transport channel and interaction of IDT type dyes on photoelectric characteristics
inferred← citeshttps://doi.org/10.1016/j.molliq.2022.120797openalex-snapshot
Revealing the photoelectric performance and multistep electron transfer mechanism in D-A-π-A dyes coupled with a chlorophyll derivative for co-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.126405openalex-snapshot
Investigation of the impact of internal acceptor and π-linker in 2, 5-di(2-thienyl)pyrrole based organic dye photosensitizer for DSSCs
inferred← citeshttps://doi.org/10.1016/j.molstruc.2018.12.052openalex-snapshot
Novel D-A-π-A type benzocarbazole sensitizers for dye sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.molstruc.2020.129367openalex-snapshot
D-A-π-A Carbazole Dyes Bearing Fluorenone Acceptor for Dye Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.142026openalex-snapshot
Graphene-decorated Indigo based Photosensitizers for DSSC applications: A DFT approach
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146450openalex-snapshot
Engineering electrically productive J-aggregation in cis-squaraine sensitizers via dual anchoring for high-performance near-IR DSSCs
inferred← citeshttps://doi.org/10.1016/j.mser.2019.100517openalex-snapshot
Device characteristics and material developments of indoor photovoltaic devices
inferred← citeshttps://doi.org/10.1016/j.mtcomm.2019.100731openalex-snapshot
Theoretical design of new triphenylamine based dyes for the fabrication of DSSCs: A DFT/TD-DFT study
inferred← citeshttps://doi.org/10.1016/j.mtsust.2022.100271openalex-snapshot
Unreported resistance in charge transport limits the photoconversion efficiency of aqueous dye-sensitised solar cells: an electrochemical impedance spectroscopy study
inferred← citeshttps://doi.org/10.1016/j.optmat.2018.01.022openalex-snapshot
D-A-π-A dye-sensitizers with Cd (Ⅱ) or Cu (Ⅱ) complex as auxiliary electron acceptor
inferred← citeshttps://doi.org/10.1016/j.orgel.2016.07.022openalex-snapshot
Panchromatic dyes having diketopyrrolopyrrole and ethylenedioxythiophene applied to dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.orgel.2016.09.014openalex-snapshot
Influence of oligothiophene-functionalized co-sensitizer on the electron injection efficiency for multiple dye-TiO2 interface
inferred← citeshttps://doi.org/10.1016/j.orgel.2016.10.024openalex-snapshot
Influence of m-fluorine substituted phenylene spacer dyes in dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.orgel.2016.12.043openalex-snapshot
Effects of different electron donating groups on dye regeneration and aggregation in phenothiazine-based dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.orgel.2017.07.019openalex-snapshot
Twisted donor substituted simple thiophene dyes retard the dye aggregation and charge recombination in dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.poly.2017.09.024openalex-snapshot
Enhancement of the photovoltaic performance in D 3 A porphyrin-based DSCs by incorporating an electron withdrawing triazole spacer
inferred← citeshttps://doi.org/10.1016/j.procbio.2025.06.006openalex-snapshot
Fast and green process to obtain astaxanthin-rich extracts from shrimp shell waste for dye sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.progpolymsci.2021.101428openalex-snapshot
Versatile Applications of Metallopolymers
inferred← citeshttps://doi.org/10.1016/j.saa.2017.01.054openalex-snapshot
Function of CN group in organic sensitizers: The first principle study
inferred← citeshttps://doi.org/10.1016/j.saa.2017.12.012openalex-snapshot
Effect of auxiliary group for p-type organic dyes in NiO-based dye-sensitized solar cells: The first principal study
inferred← citeshttps://doi.org/10.1016/j.saa.2024.123880openalex-snapshot
Screening novel candidates of ZL003-based organic dyes for dye-sensitized solar cells by modifying auxiliary electron acceptors: A theoretical study
inferred← citeshttps://doi.org/10.1016/j.saa.2025.125754openalex-snapshot
The influence of the position and quantity of thiophene or acetylene groups on the photoelectric properties of dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.saa.2026.128380openalex-snapshot
DFT investigation of thiophene-based auxiliary acceptors and π-conjugated linkers in the photosensitization mechanism of dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.saa.2026.128692openalex-snapshot
Novel benzo[1,2-d:4,5-d']bis([1,2,3]thiadiazole) electron-withdrawing building block for the design of materials with tunable photophysical properties and highly efficient luminescence
inferred← citeshttps://doi.org/10.1016/j.solener.2017.01.016openalex-snapshot
Dye-sensitized solar cells: Investigation of D-A-π-A organic sensitizers based on [1,2,5]selenadiazolo[3,4-c]pyridine
inferred← citeshttps://doi.org/10.1016/j.solener.2019.05.053openalex-snapshot
Improving energy transfer efficiency of dye-sensitized solar cell by fine tuning of dye planarity
inferred← citeshttps://doi.org/10.1016/j.solener.2020.08.001openalex-snapshot
Effect of auxiliary donors and position of benzothiadiazole on the optical and photovoltaic properties of dithieno[3,2-b:2′,3′-d]pyrrole-based sensitizers
inferred← citeshttps://doi.org/10.1016/j.solener.2020.08.084openalex-snapshot
Influence of internal acceptor and thiophene based π-spacer in D-A-π-A system on photophysical and charge transport properties for efficient DSSCs: A DFT insight
inferred← citeshttps://doi.org/10.1016/j.solener.2020.10.027openalex-snapshot
Triazatruxene-based sensitizers for highly efficient solid-state dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.solener.2022.05.043openalex-snapshot
Expanding π-bridge and introducing auxiliary acceptor for realizing panchromatic absorption of the phenothiazine dyes in dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.synthmet.2016.03.031openalex-snapshot
Toward tightly bound carboxylic acid-based organic dyes for DSCs: relative TiO2 binding strengths of benzoic acid, cyanoacrylic acid, and conjugated double carboxylic acid anchoring dyes
inferred← citeshttps://doi.org/10.1016/j.synthmet.2018.01.004openalex-snapshot
Rational tailoring of C275 towards promising organic dyes: Enhancing light absorption and charge separation
inferred← citeshttps://doi.org/10.1016/j.synthmet.2022.117137openalex-snapshot
The effect of conjugated groups for favourable molecular planarity and efficient suppression of charge recombination simultaneously of phenothiazine-based organic dyes for dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.synthmet.2023.117344openalex-snapshot
The application of a novel D−A− π − A phenothiazine-based organic dye with N719 in efficient parallel tandem dye-sensitized solar cells
inferred← citeshttps://doi.org/10.1016/j.tet.2015.08.068openalex-snapshot
D-A-π-A organic dyes for dye-sensitized solar cells: effect of π-bridge length between two acceptors on photovoltaic properties
inferred← citeshttps://doi.org/10.1016/j.tet.2016.10.057openalex-snapshot
Design of high-performance dye-sensitized solar cells by variation of the dihedral angles of dyes
inferred← citeshttps://doi.org/10.1016/j.tet.2022.132756openalex-snapshot
Novel polymeric metal complexes of salicylaldehyde schiff base derivative being used for dye sensitizer
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00807openalex-snapshot
Ultrafast Electron Dynamics in Solar Energy Conversion
inferred← citeshttps://doi.org/10.1021/acs.energyfuels.1c02955openalex-snapshot
Novel D–A−π–A Organic Dyes with Phenoxazine as a Donor Unit for Dye-Sensitized Solar Cells: The Effect of an Ethynyl Group on Performance
inferred← citeshttps://doi.org/10.1021/acs.energyfuels.4c06413openalex-snapshot
Single Component Dye-Sensitized Solar Cells Enabled by Copper Chemistry: Introduction of the Retro Cell
inferred← citeshttps://doi.org/10.1021/acs.jpca.8b09048openalex-snapshot
Photoannealing of Merocyanine Aggregates
inferred← citeshttps://doi.org/10.1021/acs.jpcc.0c00369openalex-snapshot
Effect of Electron-Withdrawing/-Donating Groups on the Sensitizing Action of the Novel Organic Dye “3-(5-(4-(Diphenylamino)styryl)thiophen-2-yl)-2-cyanoacrylic Acid” for N-Type Dye-Sensitized Solar Cells: A Theoretical Study
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.1c05051openalex-snapshot
Probing Interfacial Halogen-Bonding Effects with Halogenated Organic Dyes and a Lewis Base-Decorated Transition Metal-Based Redox Shuttle at a Metal Oxide Interface in Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acs.jpcc.7b01621openalex-snapshot
A Stable Panchromatic Green Dual Acceptor, Dual Donor Organic Dye for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acs.jpcc.7b02328openalex-snapshot
D–A−π–A System: Light Harvesting, Charge Transfer, and Molecular Designing
inferred← citeshttps://doi.org/10.1021/acs.jpcc.8b07122openalex-snapshot
Systematic Study of the Effect of Auxiliary Acceptors in D–A′−π–A Sensitizers Used on Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acs.jpcc.8b07965openalex-snapshot
Anchoring Group and π-Spacer Effects on the Dynamics and Kinetics of the Photovoltaic Processes in the Quinoxaline-Based Organic Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acs.jpcc.8b09372openalex-snapshot
CAHM1: A Theory-Based Proposal for a New DSSC D–A−π–A Dye
inferred← citeshttps://doi.org/10.1021/acs.jpcc.8b10708openalex-snapshot
Electronic Structure and Optical Properties of Designed Photo-Efficient Indoline-Based Dye-Sensitizers with D–A−π–A Framework
inferred← citeshttps://doi.org/10.1021/acs.jpcc.9b03986openalex-snapshot
Energy-Level Control via Molecular Planarization and Its Effect on Interfacial Charge-Transfer Processes in Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acs.jpcc.9b10616openalex-snapshot
First-Principles Approach for Assessing Cold Electron Injection Efficiency of Dye-Sensitized Solar Cell: Elucidation of Mechanism of Charge Injection and Recombination
inferred← citeshttps://doi.org/10.1021/acs.langmuir.7b00683openalex-snapshot
Determining the Conduction Band-Edge Potential of Solar-Cell-Relevant Nb2O5 Fabricated by Atomic Layer Deposition
inferred← citeshttps://doi.org/10.1021/acsaem.0c00464openalex-snapshot
Anthracene Organic Sensitizer with Dual Anchors for Efficient and Robust Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acsaem.0c02199openalex-snapshot
Molecular Engineering of Indoline Dyes and Their Application in Dye-Sensitized Solar Cells: Effect of Planarity and Side Chain on Interfacial Charge-Transfer Processes
inferred← citeshttps://doi.org/10.1021/acsaem.4c02977openalex-snapshot
Dual-Strategy from a Single Molecule: Low-Cost, Dopant-Free, Stable D–A–D Type Quinoxaline-Based Hole-Transporting Materials for Perovskite Solar Cells in Both Indoor and Outdoor Applications
inferred← citeshttps://doi.org/10.1021/acsaem.8b00261openalex-snapshot
Novel Organic Dyes Featuring Spiro[dibenzo[3,4:6,7]cyclohepta[1,2-b]quinoxaline-10,9′-fluorene] (SDBQX) as a Rigid Moiety for Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acsaem.8b00380openalex-snapshot
Dyad Sensitizer of Chlorophyll with Indoline Dye for Panchromatic Photocatalytic Hydrogen Evolution
inferred← citeshttps://doi.org/10.1021/acsaem.8b02100openalex-snapshot
Molecular Design Strategy toward Robust Organic Dyes in Thin-Film Photoanodes
inferred← citeshttps://doi.org/10.1021/acsami.1c00559openalex-snapshot
Structural Engineering of Organic D–A−π–A Dyes Incorporated with a Dibutyl-Fluorene Moiety for High-Performance Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acsami.1c11547openalex-snapshot
Effect of the Spatial Configuration of Donors on the Photovoltaic Performance of Double D−π–A Organic Dyes
inferred← citeshttps://doi.org/10.1021/acsami.4c15133openalex-snapshot
Umbrella-Shaped m-Terphenyls for Highly π-Extended Planar Dyes toward High-Performance Dye-Sensitized Solar Cells
inferred← citeshttps://doi.org/10.1021/acsami.5b06743openalex-snapshot
Dynamic Characteristics of Aggregation Effects of Organic Dyes in Dye-Sensitized Solar Cells
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/acsami.5b08888openalex-snapshot
Rational Molecular Engineering of Indoline-Based D-A-π-A Organic Sensitizers for Long-Wavelength-Responsive Dye-Sensitized Solar Cells
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