Abstract
Two novel donor-π-acceptor (D-π-A)-type pull-push materials, M1 and M2, having triphenylamine as a donor and dimesitylboron as an acceptor, linked through a thieno[3,2-b]thiophene (TT) π-conjugated spacer bearing different functional substituents, such as -PhCN and -Ph, were synthesized and fabricated via a solution process for OLED applications. They exhibited mega Stokes shifts of 120 nm and emissions both in the solid-state and in solution. The monomers M1 and M2 had strong intramolecular charge-transfer behaviors; the solid-state quantum yields were recorded to be 76 and 72% and the solution quantum efficiencies were determined to be 100 and 95%, respectively. The solution-processed OLEDs were fabricated using low turn-on voltages, which had performances with maximum power, current and external quantum efficiencies of around 8 lm W−1, 14.1 cd A−1 and 4.78%, respectively, displaying emission colors from blue to green and yellowish green. The materials had strong fluorescence emission colors between yellowish and bluish under UV irradiation.
Original language | English |
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Pages (from-to) | 10719-10727 |
Number of pages | 9 |
Journal | Journal of Materials Chemistry C |
Volume | 10 |
Issue number | 29 |
DOIs | |
Publication status | Published - 4 Jul 2022 |
Bibliographical note
Publisher Copyright:© 2022 The Royal Society of Chemistry.
Funding
The authors dedicate this publication to late Prof. Alasdair James Campbell for his valuable contributions to science over the years. This study was created in cooperation with Prof. Alasdair James Campbell between Imperial College and Istanbul Technical University. We thank the Higher Education Council of Turkey (YOK) and TUBITAK grants to Recep Isci (PhD, 100/2000 YOK and 2211A BIDEP/TUBITAK), 214Z297 numbered British Council TUBITAK Project and Unsped Global Lojistik, Turkey, for financial support.
Funders | Funder number |
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British Council TUBITAK | |
Higher Education Council of Turkey | |
Imperial College and Istanbul Technical University | |
YOK | 214Z297, 2211A BIDEP/TUBITAK |