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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Cleij, Thomas J.
Maastricht University
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (22/22 displayed)
- 2024Electrochemical Detection of Pseudomonas aeruginosa Quorum Sensing Molecule (S)-N-Butyryl Homoserine Lactone Using Molecularly Imprinted Polymerscitations
- 2024Electrochemical Detection of Pseudomonas aeruginosa Quorum Sensing Molecule ( S )- N -Butyryl Homoserine Lactone Using Molecularly Imprinted Polymerscitations
- 2023Recent Advances in Molecularly Imprinted Polymers for Glucose Monitoring: From Fundamental Research to Commercial Applicationcitations
- 2023Dipstick Sensor Based on Molecularly Imprinted Polymer‐Coated Screen‐Printed Electrodes for the Single‐Shot Detection of Glucose in Urine Samples—From Fundamental Study toward Point‐of‐Care Applicationcitations
- 2022Polyphosphate-Based Hydrogels as Drug-Loaded Wound Dressing: An In Vitro Studycitations
- 2021Topographical Vacuum Sealing of 3D-Printed Multiplanar Microfluidic Structurescitations
- 2015Strategy for Enhancing the Dielectric Constant of Organic Semiconductors Without Sacrificing Charge Carrier Mobility and Solubilitycitations
- 2011Phase behavior of PCBM blends with different conjugated polymerscitations
- 2011Identification and Quantification of Defect Structures in Poly(2,5-thienylene vinylene) Derivatives Prepared via the Dithiocarbamate Precursor Route by Means of NMR Spectroscopy on C-13-Labeled Polymerscitations
- 2011An Efficient Acid-Induced Conversion of Dithiocarbamate Precursor Polymers into Conjugated Materialscitations
- 2011Tetra-alkoxy substituted PPV derivatives: a new class of highly soluble liquid crystalline conjugated polymerscitations
- 2010Alkyl-Chain-Length-Independent Hole Mobility via Morphological Control with Poly(3-alkylthiophene) Nanofiberscitations
- 2010MIP-based sensor platforms for the detection of histamine in the nano- and micromolar range in aqueous mediacitations
- 2009Exploring the Dithiocarbamate Precursor Route: Observation of a Base Induced Regioregularity Excess in Poly[(2-methoxy-5-(3 ',7 '-dimethyloctyloxy))-1,4-phenylenevinylene] (MDMO-PPV)citations
- 2009Controlling the morphology of nanofiber-P3HT:PCBM blends for organic bulk heterojunction solar cellscitations
- 2008Effect of temperature on the morphological and photovoltaic stability of bulk heterojunction polymer: fullerene solar cellscitations
- 2008Charge dissociation in polymer:fullerene bulk heterojunction solar cells with enhanced permittivitycitations
- 2008NMR study of the nanomorphology in thin films of polymer blends used in organic PV devices: MDMO-PPV/PCBMcitations
- 2007The synthesis of regio-regular poly(3-alkyl-2,5-thienylene vinylene) derivatives using lithium bis(trimethylsilyl)amide (LHMDS) in the dithiocarbamate precursorcitations
- 20072,5-substituted PPV-derivatives with different polarities: The effect of side chain polarity on solubility, optical and electronic propertiescitations
- 2007The synthesis of poly(thienylene vinylene) derivatives via the dithiocarbamate route: low band gap p-type conjugated polymers for photovoltaicscitations
- 2000Occurrence of radical cation localization in chemically modified poly(methylphenylsilane): Poly(methylphenyl-co-4-dimethylaminophenylmethylsilane)s and poly (methylphenyl-co-4-bromophenylmethylsilane)scitations
Places of action
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article
Strategy for Enhancing the Dielectric Constant of Organic Semiconductors Without Sacrificing Charge Carrier Mobility and Solubility
Abstract
<p>Current organic semiconductors for organic photovoltaics (OPV) have relative dielectric constants (relative permittivities, epsilon(r)) in the range of 2-4. As a consequence, Coulombically bound electron-hole pairs (excitons) are produced upon absorption of light, giving rise to limited power conversion efficiencies. We introduce a strategy to enhance epsilon(r) of well-known donors and acceptors without breaking conjugation, degrading charge carrier mobility or altering the transport gap. The ability of ethylene glycol (EG) repeating units to rapidly reorient their dipoles with the charge redistributions in the environment was proven via density functional theory (DFT) calculations. Fullerene derivatives functionalized with triethylene glycol side chains were studied for the enhancement of epsilon(r) together with poly(p-phenylene vinylene) and diketo-pyrrolopyrrole based polymers functionalized with similar side chains. The polymers showed a doubling of epsilon(r) with respect to their reference polymers in identical backbone. Fullerene derivatives presented enhancements up to 6 compared with phenyl-C-61-butyric acid methyl ester (PCBM) as the reference. Importantly, the applied modifications did not affect the mobility of electrons and holes and provided excellent solubility in common organic solvents.</p>