Development of a functionally separated D–π-A fluorescent dye with a pyrazyl group as an electron-accepting group for dye-sensitized solar cells
Literature Information
Yousuke Ooyama, Koji Uenaka, Joji Ohshita
A functionally separated D–π-A dye OUK-3 with a pyrazyl group as an electron-withdrawing anchoring group and a carboxyl group as an additional anchoring group has been newly developed as a photosensitizer for dye-sensitized solar cells. The optical and electrochemical properties, adsorption states on TiO2 nanoparticles, and photovoltaic performances in dye-sensitized solar cells (DSSCs) were investigated. It was found that the maximum adsorption amount of dye adsorbed on the TiO2 electrode for OUK-3 is 3 times as much as that of the D–π-A dye sensitizer OUK-1 with a pyrazyl group as an electron-withdrawing anchoring group. Moreover, this work revealed that the DSSC based on the dye OUK-3 exhibits a higher photovoltage (Voc) value than the DSSC based on the dye OUK-1. On the basis of the FTIR spectra of the dyes adsorbed on TiO2 nanoparticles and the electrochemical impedance spectroscopy (EIS) analysis of DSSCs based on the two dyes OUK-1 and OUK-3, the differences of photovoltaic performances between the two dyes are discussed by taking into account the adsorption states of the dyes adsorbed on the TiO2 surface. This work demonstrates that functionally separated D–π-A dye sensitizers can achieve effective surface coverage of the TiO2 electrode due to their high adsorption ability onto the TiO2 electrode, leading to not only the improvement of light-harvesting efficiency (LHE), but also an increase in the number of injected electrons in the CB of TiO2, which is responsible for the higher Voc value of functionally separated D–π-A dye sensitizers.
Related Literature
Conformational dynamics for chemical sensing: simplicity and diversity
Justin A. Riddle, Xuan Jiang, Dongwhan Lee
DOI: 10.1039/B715673C
Determination of enzyme kinetics and glutathione conjugates of chlortetracycline and chloroacetanilides using liquid chromatography–mass spectrometry
Michael Farkas, James O. Berry, Diana S. Aga
DOI: 10.1039/B700561J
A review of biosensors and biologically-inspired systems for explosives detection‡
Richard G. Smith, Natasha D'Souza, Stephen Nicklin
DOI: 10.1039/B717933M
Ratiometric photoacoustic sensing of pH using a “sonophore”
Thomas D. Horvath, Gwangseong Kim, Raoul Kopelman, Shai Ashkenazi
DOI: 10.1039/B800116B
Aqueous synthesis of type-II core/shell CdTe/CdSe quantum dots for near-infrared fluorescent sensing of copper(ii)‡
Yunsheng Xia, Changqing Zhu
DOI: 10.1039/B801963K
In situ monitoring of the seed stage of a fermentation process using non-invasive NIR spectrometry
Alison Nordon, David Littlejohn, Alison S. Dann, Paul A. Jeffkins, Mark D. Richardson, Sarah L. Stimpson
DOI: 10.1039/B719318A
Quadruple-allele chemiluminometric assay for simultaneous genotyping of two single-nucleotide polymorphisms
Dimitrios S. Elenis, Penelope C. Ioannou
DOI: 10.1039/B818516F
Hybridization kinetics of double-stranded DNA probes for rapid molecular analysis
Vinay Gidwani, Reza Riahi, Donna D. Zhang
DOI: 10.1039/B906077D
The development of an immobilized enzyme reactor containing glyceraldehyde-3-phosphate dehydrogenase from Trypanosoma cruzi: the effect of species' specific differences on the immobilization
Carmen Lúcia Cardoso, Marcela Cristina de Moraes, Rafael Victorio Carvalho Guido, Glaucius Oliva, Adriano Defini Andricopulo, Irving William Wainer, Quezia Bezerra Cass
DOI: 10.1039/B711145B
Establishing SI traceability for measurements of mercury vapour
Andrew S. Brown, Richard J. C. Brown, Warren T. Corns, Peter B. Stockwell
DOI: 10.1039/B803724H
You might also like
Is 2-(2-chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) safe?
2-(2-Chloroacetamido)-3-phenylpropanoic acid (CAS: 7765-11-9) is generally consi...
Is 2-(Benzyloxy)-5-bromobenzoic acid (CAS: 62176-31-2) safe?
2-(Benzyloxy)-5-bromobenzoic acid can be handled safely if appropriate precautio...
What is (4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride (CAS: 1159825-48-5)?
(4-Methyl-1,2,5-oxadiazol-3-yl)methanamine hydrochloride is a chemical compound ...
What is 2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54-7)?
2-(5-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS: 917985-54...
Are there alternatives to 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS: 102771-26-6) in synthesis?
While 4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine (CAS:...
What is the market or research trend for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine-6-carboxylate (CAS: 851376-80-2)?
The market for tert-butyl 3-hydroxy-4,5,7,8-tetrahydro-2H-pyrazolo[3,4-d]azepine...
How should waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) be handled?
Waste containing 3,5-Diamino-1H-pyrazole-4-carbonitrile (CAS: 6844-58-2) should ...
How is (6-Fluoro-3-pyridinyl)boronic acid (CAS: 351019-18-6) typically synthesized?
(6-Fluoro-3-pyridinyl)boronic acid can be synthesized through the reaction of 6-...
What industries use Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9)?
Dibenzyl carbonimidoylbiscarbamate (CAS: 10065-79-9) finds applications in vario...
What is the market or research trend for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4)?
The market for (beta,beta,2,3,4,5,6-~2~H_7_)Phenylalanine (CAS: 74228-83-4) is g...
Source Journal
Organic Chemistry Frontiers

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry










![(1R)-N-((1R)-1-Phenylethyl)-1-[4-(tert-butyldimethylsilyloxymethyl)cyclohexyl]ethan-1-amine structure (1R)-N-((1R)-1-Phenylethyl)-1-[4-(tert-butyldimethylsilyloxymethyl)cyclohexyl]ethan-1-amine structure](https://static.chemtradehub.com/structs/672/672314-45-3-47ef.webp)


![3,7-Di(1,1':3',1''-terphenyl-5'-yl)-10,11,12,13-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-ol 5-oxide structure 3,7-Di(1,1':3',1''-terphenyl-5'-yl)-10,11,12,13-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-ol 5-oxide structure](https://static.chemtradehub.com/structs/135/1352810-38-8-3f10.webp)
