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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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Havenith, Remco W. A.
University of Groningen
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (22/22 displayed)
- 2024Lattice Dynamics and Thermoelectric Properties of 2D LiAlTe 2 , LiGaTe 2 , and LiInTe 2 Monolayerscitations
- 2024Lattice Dynamics and Thermoelectric Properties of 2D LiAlTe2, LiGaTe2, and LiInTe2 Monolayerscitations
- 2023Spark Discharge Doping—Achieving Unprecedented Control over Aggregate Fraction and Backbone Ordering in Poly(3‐hexylthiophene) Solutionscitations
- 2022Strategies for Enhancing the Dielectric Constant of Organic Materialscitations
- 2022Strategies for Enhancing the Dielectric Constant of Organic Materialscitations
- 2021Amphipathic Side Chain of a Conjugated Polymer Optimizes Dopant Location toward Efficient N-Type Organic Thermoelectricscitations
- 2021Amphipathic Side Chain of a Conjugated Polymer Optimizes Dopant Location toward Efficient N-Type Organic Thermoelectricscitations
- 2020N-type organic thermoelectrics:demonstration of ZT > 0.3citations
- 2020How Ethylene Glycol Chains Enhance the Dielectric Constant of Organic Semiconductors:Molecular Origin and Frequency Dependencecitations
- 2020How Ethylene Glycol Chains Enhance the Dielectric Constant of Organic Semiconductorscitations
- 2020N-type organic thermoelectricscitations
- 2019Coverage-Controlled Polymorphism of H-Bonded Networks on Au(111)citations
- 2015Strategy for Enhancing the Dielectric Constant of Organic Semiconductors Without Sacrificing Charge Carrier Mobility and Solubilitycitations
- 2015Strategy for Enhancing the Dielectric Constant of Organic Semiconductors Without Sacrificing Charge Carrier Mobility and Solubility
- 2014Strategy for Enhancing the Electric Permittivity of Organic Semiconductors
- 2014Stabilizing cations in the backbones of conjugated polymerscitations
- 2014Stabilizing cations in the backbones of conjugated polymerscitations
- 2013Molecular flexibility and structural instabilities in crystalline L-methioninecitations
- 2007On the structure of cross-conjugated 2,3-diphenylbutadienecitations
- 2002Ring current and electron delocalisation in an all-metal cluster, Al42-citations
- 2000Infinite, undulating chains of intermolecularly hydrogen bonded (E,E)-2,2-dimethylcyclohexane-1,3-dione dioximes in the solid state. A single crystal X-ray, charge density distribution and spectroscopic studycitations
- 2000Infinite, undulating chains of intermolecularly hydrogen bonded (E,E)-2,2-dimethylcyclohexane-1,3-dione dioximes in the solid state. A single crystal X-ray, charge density distribution and spectroscopic studycitations
Places of action
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article
Stabilizing cations in the backbones of conjugated polymers
Abstract
<p>We synthesized a cross-conjugated polymer containing ketones in the backbone and converted it to a linearly conjugated, cationic polyarylmethine via a process we call "spinless doping" to create a new class of materials, conjugated polyions. This process involves activating the ketones with a Lewis acid and converting them to trivalent cations via the nucleophilic addition of electron-rich aryl moieties. Spinless doping lowers the optical band gap from 3.26 to 1.55 eV while leaving the intrinsic semiconductor properties of the polymer intact. Electrochemical reduction (traditional doping) further decreases the predicted gap to 1.18 eV and introduces radicals to form positive polarons; here, n-doping produces a p-doped polymer in its metallic state. Treatment with a nucleophile (NaOMe) converts the cationic polymer to a neutral, non-conjugated state, allowing the band gap to be tuned chemically, postpolymerization. The synthesis of these materials is carried out entirely without the use of Sn or Pd and relies on scalable Friedel-Crafts chemistry.</p>