Highly-efficient metal-free organic dyes for dye-sensitized solar cells
Literature Information
Tamotsu Horiuchi, Hidetoshi Miura, Satoshi Uchida
A solar-to-electric conversion efficiency of 6.1% is achieved with this new dye, compared to 6.3% for N3 dye under the same experimental conditions. Although these indoline dyes are slightly less efficient than N3 dye, the cost of indoline dye is much less than for N3 due to ease of preparation. Furthermore, indoline dyes are shown to be highly stable to photoredox processes by cyclic voltammogram.
Related Literature
DNP NMR spectroscopy of cross-linked organic polymers: rational guidelines towards optimal sample preparation
Wei-Chih Liao, Atsuko Ogawa, Kazuhiko Sato, Christophe Copéret
DOI: 10.1039/C9CP05208A
Correction: Isomer-specific cryogenic ion vibrational spectroscopy of the D2 tagged Cs+(HNO3)(H2O)n=0–2 complexes: ion-driven enhancement of the acidic H-bond to water
Sayoni Mitra, Chinh H. Duong, Mark A. Johnson
DOI: 10.1039/D0CP90054K
The challenging playground of astrochemistry: an integrated rotational spectroscopy – quantum chemistry strategy
Cristina Puzzarini, Vincenzo Barone
DOI: 10.1039/D0CP00561D
Specific ion effects on the enzymatic activity of alcohol dehydrogenase from Saccharomyces cerevisiae
Andrea Salis, Edmond Magner
DOI: 10.1039/C9CP06800G
Theoretical study on thermal curing mechanism of arylethynyl-containing resins
Zuowei Chen, Liquan Wang, Jiaping Lin, Lei Du
DOI: 10.1039/C9CP06892A
Effects of electrospray mechanisms and structural relaxation on polylactide ion conformations in the gas phase: insights from ion mobility spectrometry and molecular dynamics simulations
Haidy Metwally, Vincent Lemaur, Jérôme Cornil, Julien De Winter, Lars Konermann, Pascal Gerbaux
DOI: 10.1039/C9CP06391A
Halogen⋯halogen interactions in decahalo-closo-carboranes: CSD analysis and theoretical study
Maria de las Nieves Piña, Antonio Bauzá, Antonio Frontera
DOI: 10.1039/D0CP00114G
Molecular dynamics simulations of alkaline earth metal ions binding to DNA reveal ion size and hydration effects
Makenzie Provorse Long, Serra Alland, Madison E. Martin, Christine M. Isborn
DOI: 10.1039/C9CP06844A
Role of ring-enlargement reactions in the formation of aromatic hydrocarbons
Martina Baroncelli, Qian Mao, Simon Galle, Nils Hansen, Heinz Pitsch
DOI: 10.1039/C9CP05854K
You might also like
What precautions should be taken when handling lithium chloride hydrate (1:1:1) (CAS: 16712-20-2)?
When handling lithium chloride hydrate (1:1:1) (CAS: 16712-20-2), it is importan...
Is 4-(4H-1,2,4-Triazol-4-yl)piperidine (CAS: 690261-92-8) safe?
4-(4H-1,2,4-Triazol-4-yl)piperidine is generally considered safe for use in phar...
How should waste containing 1,3-Thiazole-2-carboxamide (CAS: 16733-85-0) be handled?
Waste containing 1,3-Thiazole-2-carboxamide (CAS: 16733-85-0) should be collecte...
What regulatory guidelines apply to 5-(Difluoromethyl)-2-fluorobenzonitrile (CAS: 934175-58-3)?
5-(Difluoromethyl)-2-fluorobenzonitrile (CAS: 934175-58-3) is subject to regulat...
How is Methyl 3-acetamido-2-thiophenecarboxylate (CAS: 22288-79-5) typically synthesized?
Methyl 3-acetamido-2-thiophenecarboxylate can be synthesized by the reaction of ...
What is 4-Isoquinolinecarbonitrile (CAS: 34846-65-6)?
4-Isoquinolinecarbonitrile is a chemical compound with the CAS number 34846-65-6...
How should Methyl 1H-1,2,3-triazole-4-carboxylate (CAS: 877309-59-6) be stored?
Store Methyl 1H-1,2,3-triazole-4-carboxylate (CAS: 877309-59-6) in a cool, dry p...
What regulatory guidelines apply to 6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine (CAS: 1160791-13-8)?
6-Bromo[1,3]thiazolo[5,4-b]pyridin-2-amine (CAS: 1160791-13-8) is subject to the...
Is (2S,3S)-2-Ammonio-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoate (CAS: 23651-95-8) safe?
(2S,3S)-2-Ammonio-3-(3,4-dihydroxyphenyl)-3-hydroxypropanoate (CAS: 23651-95-8) ...
What are the physical and chemical properties of 7-bromo-3-methyl-3,4-dihydroquinazolin-4-one (CAS: 1293987-84-4)?
7-Bromo-3-methyl-3,4-dihydroquinazolin-4-one is a solid with a crystalline form....
Source Journal
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry










![(R)-N-[(S)-1-[2-(Diphenylphosphino)phenyl]ethyl]-2-methylpropane-2-sulfinamide structure (R)-N-[(S)-1-[2-(Diphenylphosphino)phenyl]ethyl]-2-methylpropane-2-sulfinamide structure](https://static.chemtradehub.com/structs/159/1595319-98-4-33e7.webp)
![[(2R)-6,6-Dimethyl-2-morpholinyl]methanol hydrochloride (1:1) structure [(2R)-6,6-Dimethyl-2-morpholinyl]methanol hydrochloride (1:1) structure](https://static.chemtradehub.com/structs/141/1416444-88-6-e06a.webp)
![tert-butyl 8-benzyl-2,8-diazaspiro[4.5]decane-2-carboxylate structure tert-butyl 8-benzyl-2,8-diazaspiro[4.5]decane-2-carboxylate structure](https://static.chemtradehub.com/structs/336/336191-16-3-bb55.webp)
![Ethyl 4-[8-chloro(5,5,6,6,7-~2~H_5_)-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene]-1-piperidinecarboxylate structure Ethyl 4-[8-chloro(5,5,6,6,7-~2~H_5_)-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene]-1-piperidinecarboxylate structure](https://static.chemtradehub.com/structs/102/1020719-57-6-37e2.webp)
