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https://hdl.handle.net/10442/19036
Εξειδίκευση τύπου : | Άρθρο σε επιστημονικό περιοδικό |
Τίτλος: | Rational Design of New Conjugated Polymers with Main Chain Chirality for Efficient Optoelectronic Devices: Carbo[6]Helicene and Indacenodithiophene Copolymers as Model Compounds |
Δημιουργός/Συγγραφέας: | Gedeon, Clement Rio, Natalia Del Furlan, Francesco Taddeucci, Andrea Vanthuyne, Nicolas [EL] Γρηγορίου, Βασίλης Γ.[EN] Gregoriou, Vasilis G. Fuchter, Matthew J Siligardi, Giuliano Gasparini, Nicola Crassous, Jeanne [EL] Χώχος, Χρήστος[EN] Chochos, Christos |
Εκδότης: | Wiley |
Ημερομηνία: | 2024-02-26 |
Γλώσσα: | Αγγλικά |
ISSN: | 0935-9648 1521-4095 |
DOI: | 10.1002/adma.202314337 |
Άλλο: | 38406997 |
Περίληψη: | The unique properties of conjugated polymers (CPs) in various optoelectronic applications are mainly attributed to their different self-assembly processes and superstructures. Various methods have been utilized to tune and control CP structure and properties with less attention paid to the use of chirality. CPs with main chain chirality are rare and their microscopic and macroscopic properties are still unknown. In this work, we provide the first experimental results along these lines by synthesizing a series of racemic and enantiopure CPs containing statistical and alternating carbo[6]helicene and indacenodithiophene moieties and evaluating their microscopic (optical, energy levels) and macroscopic properties (hole mobilities, photovoltaic performance). We demonstrate that a small statistical insertion of either the racemic or enantiopure helicene into the polymer backbone finely tunes the microscopic and macroscopic properties as a function of the statistical content. The microscopic properties of the enantiopure versus the racemic polymers with the same helicene loading remain similar. On the contrary, the macroscopic properties, and more interestingly those between the two enantiomeric forms, are altered as a function of the statistical content. Once incorporated into a solar cell device, these chiral CPs display better performance in their enantiopure versus racemic forms. This article is protected by copyright. All rights reserved. |
Τίτλος πηγής δημοσίευσης: | Advanced materials (Deerfield Beach, Fla.) |
Θεματική Κατηγορία: | [EL] Φασματοσκοπία[EN] Spectroscopy [EL] Χημική τεχνολογία[EN] Chemical technolgy [EL] Χημική μηχανική[EN] Chemical engineering [EL] Χημικά προϊόντα: Παραγωγή, χρήση κλπ[EN] Chemicals: Manufacture, use etc. |
Λέξεις-Κλειδιά: | Chirality Helicene Organic Solar Cells (OSC) Self-assembly Π-conjugated polymers |
EU Grant identifier: | 859752 –HEL4CHIROLED –H2020-MSCA-ITN-2019 EP/R00188X/1 4694 |
Όροι και προϋποθέσεις δικαιωμάτων: | This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
Ηλεκτρονική διεύθυνση στον εκδότη (link): | https://doi.org/10.1002/adma.202314337 |
Σημειώσεις: | Post-print article (accepted version) |
Εμφανίζεται στις συλλογές: | Ινστιτούτο Χημικής Βιολογίας - Επιστημονικό έργο
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