Efficient co-sensitization of nanocrystalline TiO2 films by organic sensitizers
Literature Information
Jun-Ho Yum, Song-Rim Jang, Pablo Walter, T. Geiger, F. Nüesch, Sanghoon Kim, Jaejung Ko, Michael Grätzel, Mohammad K. Nazeeruddin
Dye-sensitized solar cells based on co-sensitization of organic dyes having complementary spectral absorption in the visible region resulted in a panchromatic response, which exhibited 86% incident monochromatic photon-to-current conversion efficiency in the visible region; the optimized cell gave a short circuit current density of 15.5 mA cm−2, an open circuit voltage of 685 mV and a fill factor of 0.70 corresponding to an overall conversion efficiency of 7.43% under solar simulated light irradiation of 100 mW cm−2.
Related Literature
Molecular basis for competitive solvation of the Burkholderia cepacia lipase by sorbitol and urea
Ivan P. Oliveira, Leandro Martínez
DOI: 10.1039/C6CP01789D
Cysteine containing dipeptides show a metal specificity that matches the composition of seawater
Luca Belmonte, Daniele Rossetto, Michele Forlin, Simone Scintilla, Claudia Bonfio, Sheref S. Mansy
DOI: 10.1039/C6CP00608F
The properties of substituted 3D-aromatic neutral carboranes: the potential for σ-hole bonding
Rabindranath Lo, Jindřich Fanfrlík, Martin Lepšík
DOI: 10.1039/C5CP03617H
Interlayer coupling in two-dimensional titanium carbide MXenes
Chao Zhang, Jingyang Wang, Xiaohui Wang
DOI: 10.1039/C6CP01699E
Computational simulation and interpretation of the low-lying excited electronic states and electronic spectrum of thioanisole
Shaohong L. Li, Xuefei Xu, Donald G. Truhlar
DOI: 10.1039/C5CP02461G
Correction: Kinetics and mechanism of the reaction of perfluoro propyl vinyl ether (PPVE, C3F7OCHCH2) with OH: assessment of its fate in the atmosphere
D. Amedro, L. Vereecken, J. N. Crowley
DOI: 10.1039/C5CP90133B
Water sorption behaviour of two series of PHA/montmorillonite films and determination of the mean water cluster size
N. Follain, R. Crétois, L. Lebrun, S. Marais
DOI: 10.1039/C6CP04147G
Spontaneously electrical solids in a new light
Jérôme Lasne, Alexander Rosu-Finsen, Andrew Cassidy, Martin R. S. McCoustra, David Field
DOI: 10.1039/C5CP03174E
You might also like
What is 1-(2,4,6-Trifluorophenyl)ethanol (CAS: 1250113-83-7)?
1-(2,4,6-Trifluorophenyl)ethanol is an organic compound with the CAS number 1250...
Is 1-(2,4-Dimethoxybenzyl)-4-(hydroxymethyl)-2-pyrrolidinone (CAS: 919111-34-5) safe?
1-(2,4-Dimethoxybenzyl)-4-(hydroxymethyl)-2-pyrrolidinone (CAS: 919111-34-5) is ...
What are the physical and chemical properties of (7S,15R)-6β,15-Diacetoxy-7α,20-epoxy-7-hydroxykaura-2,16-dien-1-one (CAS: 51419-51-3)?
(7S,15R)-6β,15-Diacetoxy-7α,20-epoxy-7-hydroxykaura-2,16-dien-1-one is a crystal...
What regulatory guidelines apply to rac-ethyl (1r,4r)-4-hydroxycyclohexane-1-carboxylate, trans (CAS: 3618-04-0)?
The compound rac-ethyl (1r,4r)-4-hydroxycyclohexane-1-carboxylate, trans (CAS: 3...
What is the market or research trend for 2-(2,4-Difluorophenoxy)-3-nitropyridine (CAS: 175135-62-3)?
The market for 2-(2,4-Difluorophenoxy)-3-nitropyridine (CAS: 175135-62-3) is cur...
What are the main uses of 6-Diazo-5-oxo-L-norleucine (CAS: 157-03-9)?
The main uses of 6-Diazo-5-oxo-L-norleucine (CAS: 157-03-9) include research in ...
What precautions should be taken when handling 2-Aminoethyl-mono-amide-DOTA-tris(tBu ester) (CAS: 173308-19-5)?
When handling 2-Aminoethyl-mono-amide-DOTA-tris(tBu ester) (CAS: 173308-19-5), i...
How is 5-Methylimidazo[1,2-a]pyridine-3-carbaldehyde (CAS: 178488-37-4) typically synthesized?
5-Methylimidazo[1,2-a]pyridine-3-carbaldehyde (CAS: 178488-37-4) can be synthesi...
Are there alternatives to 2,4,6-Trihydroxyisophthalaldehyde (CAS: 4396-13-8) in synthesis?
There are alternative reagents that can be used in the synthesis of 2,4,6-Trihyd...
What is (2Z)-3-(5-Fluoro-1H-indol-3-yl)-2-sulfanylacrylic acid (CAS: 179461-52-0)?
(2Z)-3-(5-Fluoro-1H-indol-3-yl)-2-sulfanylacrylic acid is a chemical compound wi...
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














