Significant Improvement of Dye-Sensitized Solar Cell Performance by Small Structural Modification in π-Conjugated Donor-Acceptor Dyes
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Data mining with molecular design rules identifies new class of dyes for dye-sensitised solar cells.Rational molecular engineering of cyclopentadithiophene-bridged D-A-π-A sensitizers combining high photovoltaic efficiency with rapid dye adsorptionOrganic 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.Vegetable-based dye-sensitized solar cells.Efficiency Records in Mesoscopic Dye-Sensitized Solar Cells.Metal-Free Sensitizers for Dye-Sensitized Solar Cells.Structure-performance correlations of organic dyes with an electron-deficient diphenylquinoxaline moiety for dye-sensitized solar cells.Status of dye solar cell technology as a guideline for further research.π-Extension of a 4-ethoxy-1,3-thiazole via aryl alkyne cross coupling: synthesis and exploration of the electronic structure.A robust organic dye for dye sensitized solar cells based on iodine/iodide electrolytes combining high efficiency and outstanding stability.Novel Ru(II) sensitizers bearing an unsymmetrical pyridine-quinoline hybrid ligand with extended π-conjugation: synthesis and application in dye-sensitized solar cells.Benzotriazole-containing D-π-A conjugated organic dyes for dye-sensitized solar cells.Photoinduced electron transfer of platinum(II) bipyridine diacetylides linked by triphenylamine- and naphthaleneimide-derivatives and their application to photoelectric conversion systems.Computational study of porphyrin-based dyes with better performance.Hydrothermal growth of TiO2 nanorod arrays and in situ conversion to nanotube arrays for highly efficient quantum dot-sensitized solar cells.Structure-property relationships for three indoline dyes used in dye-sensitized solar cells: TDDFT study of visible absorption and photoinduced charge-transfer processes.Photoinduced ultrafast dynamics of the triphenylamine-based organic sensitizer D35 on TiO2, ZrO2 and in acetonitrile.Electron and hole transfer dynamics of a triarylamine-based dye with peripheral hole acceptors on TiO2 in the absence and presence of solvent.Near-Infrared-Absorbing Metal-Free Organic, Porphyrin, and Phthalocyanine Sensitizers for Panchromatic Dye-Sensitized Solar Cells.A Perylene-Based Polycyclic Aromatic Hydrocarbon Electron Donor for a Highly Efficient Solar Cell Dye.The role of π-linkers in tuning the optoelectronic properties of triphenylamine derivatives for solar cell applications - A DFT/TDDFT study.Effect of Donor Strength and Bulk on Thieno[3,4-b]-pyrazine-Based Panchromatic Dyes in Dye-Sensitized Solar Cells.Aggregation-Induced Emission and Sensing Characteristics of Triarylborane-Oligothiophene-Dicyanovinyl Triads.Molecular engineering of panchromatic isoindigo sensitizers for dye-sensitized solar cell applications.Fine tuning the performance of DSSCs by variation of the π-spacers in organic dyes that contain a 2,7-diaminofluorene donor.Synthesis of organic photosensitizers containing dithienogermole and thiadiazolo[3,4-c]pyridine units for dye-sensitized solar cells.Near-infrared squaraine co-sensitizer for high-efficiency dye-sensitized solar cells.Novel porphyrin-preparation, characterization, and applications in solar energy conversion.Modification of D-A-π-A configuration toward a high-performance triphenylamine-based sensitizer for dye-sensitized solar cells: a theoretical investigation.Molecular Engineering of Pyrido[3,4-b]pyrazine-Based Donor-Acceptor-π-Acceptor Organic Sensitizers: Effect of Auxiliary Acceptor in Cobalt- and Iodine-Based Electrolytes.Molecular engineering of push-pull porphyrin dyes for highly efficient dye-sensitized solar cells: the role of benzene spacers.Molecular design principle of all-organic dyes for dye-sensitized solar cells.Structural control of hierarchically-ordered TiO2 films by water for dye-sensitized solar cells.Benzimidazole/Pyridoimidazole-Based Organic Sensitizers for High-Performance Dye-Sensitized Solar Cells.Unprecedentedly targeted customization of molecular energy levels with auxiliary-groups in organic solar cell sensitizers.New pyrido[3,4-b]pyrazine-based sensitizers for efficient and stable dye-sensitized solar cellsStructure–property relationship of naphthalene based donor–π–acceptor organic dyes for dye-sensitized solar cells: remarkable improvement of open-circuit photovoltageThree novel bis carbazole organic dyes for dye-sensitized solar cellsPhenothiazine–triphenylamine based organic dyes containing various conjugated linkers for efficient dye-sensitized solar cellsA Ruthenium-Based Light-Harvesting Antenna Bearing an Anthracene Moiety in Dye-Sensitized Solar Cells
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P2860
Significant Improvement of Dye-Sensitized Solar Cell Performance by Small Structural Modification in π-Conjugated Donor-Acceptor Dyes
description
im Januar 2012 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 2012
@uk
name
Significant Improvement of Dye ...... Conjugated Donor-Acceptor Dyes
@en
Significant Improvement of Dye ...... Conjugated Donor-Acceptor Dyes
@nl
type
label
Significant Improvement of Dye ...... Conjugated Donor-Acceptor Dyes
@en
Significant Improvement of Dye ...... Conjugated Donor-Acceptor Dyes
@nl
prefLabel
Significant Improvement of Dye ...... Conjugated Donor-Acceptor Dyes
@en
Significant Improvement of Dye ...... Conjugated Donor-Acceptor Dyes
@nl
P2093
P2860
P50
P356
P1476
Significant Improvement of Dye ...... Conjugated Donor-Acceptor Dyes
@en
P2093
Amaresh Mishra
Jacques-E. Moser
Joël Teuscher
Magdalena Marszalek
Mateusz Wielopolski
Peter Bäuerle
Stefan Haid
P2860
P304
P356
10.1002/ADFM.201102519
P407
P577
2012-01-26T00:00:00Z