High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye.
about
Elucidating the structure-property relationships of donor-π-acceptor dyes for dye-sensitized solar cells (DSSCs) through rapid library synthesis by a one-pot procedure.Ultrafast charge-transfer reactions of indoline dyes with anchoring alkyl chains of varying length in mesoporous ZnO solar cells.Metal-free organic dyes for TiO2 and ZnO dye-sensitized solar cells.Sensitizer molecular structure-device efficiency relationship in dye sensitized solar cells.Photophysical and electrochemical properties, and molecular structures of organic dyes for dye-sensitized solar cells.Phosphorus-containing materials for organic electronics.Co-adsorbents: a key component in efficient and robust dye-sensitized solar cells.Vegetable-based dye-sensitized solar cells.Efficiency Records in Mesoscopic Dye-Sensitized Solar Cells.Applications of Fluorogens with Rotor Structures in Solar Cells.Surface Structure Modification of ZnO and the Impact on Electronic Properties.Covalent Design for Dye-Sensitized H2-Evolving Photocathodes Based on a Cobalt Diimine-Dioxime Catalyst.Light-driven water oxidation for solar fuelsIsomerization and Aggregation of the Solar Cell Dye D149.A Quasi-Solid State DSSC with 10.1% Efficiency through Molecular Design of the Charge-Separation and -Transport.Intermolecular [3+2] cycloaddition of cyclopropylamines with olefins by visible-light photocatalysisInteractions of the N3 dye with the iodide redox shuttle: quantum chemical mechanistic studies of the dye regeneration in the dye-sensitized solar cell.The role of π bridges in high-efficiency DSCs based on unsymmetrical squaraines.High Energy Conversion Efficiency with 3-D Micro-Patterned Photoanode for Enhancement Diffusivity and Modification of Photon Distribution in Dye-Sensitized Solar Cells.Molecular engineering of organic sensitizers with planar bridging units for efficient dye-sensitized solar cells.Efficient dye-sensitized solar cells using a tetramethylthiourea redox mediator.New di-anchoring A-π-D-π-A configured organic chromophores for DSSC application: sensitization and co-sensitization studies.A General Strategy to Enhance the Performance of Dye-Sensitized Solar Cells by Incorporating a Light-Harvesting Dye with a Hydrophobic Polydiacetylene Electrolyte-Blocking Layer.Multimolecular assemblies on high surface area metal oxides and their role in interfacial energy and electron transfer.Adsorption of organic dyes on TiO2 surfaces in dye-sensitized solar cells: interplay of theory and experiment.Controlling light absorption and photoelectric properties of coumarin-triphenylaminedye by different acceptor functional groups.A low bandgap asymmetrical squaraine for high-performance solution-processed small molecule organic solar cells.Triarylamine-substituted imidazole- and quinoxaline-fused push-pull porphyrins for dye-sensitized solar cells.Donor-π-acceptors containing the 10-(1,3-dithiol-2-ylidene)anthracene unit for dye-sensitized solar cells.Diketopyrrolopyrrole-porphyrin conjugates as broadly absorbing sensitizers for dye-sensitized solar cells.Tuning the spectroscopic, electrochemical, and photovoltaic properties of triaryl amine based sensitizers through ring-fused thiophene bridges.Ultrafast photoinduced relaxation dynamics of the indoline dye D149 in organic solvents.Ruthenium sensitizer with a thienylvinylbipyridyl ligand for dye-sensitized solar cells.Bisquinoxaline-fused porphyrins for dye-sensitized solar cells.Charge Transfer Enhancement in the D-π-A Type Porphyrin Dyes: A Density Functional Theory (DFT) and Time-Dependent Density Functional Theory (TD-DFT) Study.Molecular Design Principles for Near-Infrared Absorbing and Emitting Indolizine Dyes.Rapid Synthesis of D-A'-π-A Dyes through a One-Pot Three-Component Suzuki-Miyaura Coupling and an Evaluation of their Photovoltaic Properties for Use in Dye-Sensitized Solar Cells.Does the position of the electron-donating nitrogen atom in the ring system influence the efficiency of a dye-sensitized solar cell? A computational study.Can silicon substituted metal-free organic dyes achieve better efficiency compared to silicon free organic dyes? A computational study.Modification of D-A-π-A configuration toward a high-performance triphenylamine-based sensitizer for dye-sensitized solar cells: a theoretical investigation.
P2860
Q35193018-BA0FFBAD-17B2-4E7D-B2DB-2BBA84B756A0Q35555296-DA968708-9541-43E3-B829-48DA9071E69AQ36438607-BD579E71-2B36-4182-9B74-4D7E273380CBQ37809476-7B83F00A-C49E-4DBE-99B8-D2043B566366Q38027127-B905F7FE-3E58-4FB9-9984-445E5CD4BE1BQ38200080-40B010C2-EB4D-445F-A719-7CD4D2AF0B5BQ38343880-2FDA42C2-D0D1-4CC1-B2C9-395DE4D95801Q38412082-1197D0AD-74EC-4508-89E7-736299461D49Q38548892-CA283612-DCCC-4666-8EC3-943B2F9C47AEQ38677617-F75B2962-60E7-4B2B-BA70-B91CE3865A94Q38758504-4E0A134B-FF72-4704-B046-A687CB9CB7BBQ41674571-5208FAEC-7D4B-4F4E-8404-B99C3EDA3D70Q41842435-905941E2-F684-4F79-9A2D-4A2684458EF1Q41849453-7FB9E52A-6808-409D-909A-5AEA96DC387FQ42072165-32605017-2A98-45CB-B9DA-9C16F9993B7EQ42146512-6716672D-E5B1-4940-8758-5FEFFECA27ABQ43698892-C23CC95E-719A-4478-8D10-F007E845E76EQ44076121-07243A8A-605D-4085-9D46-042510D0CA7CQ44132290-C2A9589C-2F74-4F08-B73C-9BEAD2896E82Q46094913-57E77411-A335-47C1-A28C-783031BE46A4Q46404713-0A156891-DB53-436E-8646-870859B62DAFQ48237651-D716909A-95C7-4684-9890-46F74FA37EB0Q48872703-FA5131AA-23F8-417D-8098-ABDF21C353BDQ49946026-24AC2B3A-EF4A-4746-87CD-8E035CE52F95Q50057934-34E0223D-3D3A-40F7-B732-BAD87FCAFA5FQ50225595-1B3250D0-EDD4-479A-98E9-4FF193A27B65Q50453364-1F01B19E-25EF-4A3F-9143-A851190C3DC2Q50495310-18C6A3B5-02A7-4D0B-B2B6-0B39655439F0Q50505733-C577417C-5731-487A-A59F-5B43314726DAQ50506970-4B888430-61E9-4DCF-A184-4BE9D8E0B0C5Q50518071-DC23853D-465F-4E3B-8DD2-985533153726Q50524877-320FF30E-3D8F-4008-BFC0-02B3DEF51331Q50529027-40E8F6E9-370E-4346-A2E5-5FAC4FA0F117Q50536218-EDFDA5DF-9A09-4998-8A65-CAAD896FABD3Q51038072-C5279F10-90CD-4B3B-BE0B-A9767B95C8ABQ51165961-0BB06819-20D5-4682-8E3A-31CAB4566777Q51555500-1B59B706-4E2E-42CA-ABFE-B99B7A6167F8Q51571655-3B8C7589-0CFB-462C-A66A-F7E6FA6DF3A9Q51575879-4D13D432-2A37-497B-9D07-E934C3C22F7CQ51584887-7D7C8CD1-90B5-46D5-94FE-874956FDCCF1
P2860
High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye.
@en
High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye.
@nl
type
label
High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye.
@en
High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye.
@nl
prefLabel
High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye.
@en
High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye.
@nl
P2093
P356
P1476
High-conversion-efficiency organic dye-sensitized solar cells with a novel indoline dye.
@en
P2093
Hidetoshi Miura
Koichi Sumioka
Masakazu Takata
Pascal Comte
Paul Liska
Peter Péchy
Satoshi Uchida
P304
P356
10.1039/B809093A
P407
P577
2008-09-12T00:00:00Z