Issue 10, 2022

Molecular design of DBA-type five-membered heterocyclic rings to achieve 200% exciton utilization for electroluminescence

Abstract

Achieving high exciton utilization is a long-cherished goal in the development of organic light-emitting diode materials. Herein, a three-step mechanism is proposed to achieve 200% exciton utilization: (i) hot triplet exciton (T2) conversion to singlet S1; (ii) singlet fission from S1 into two T1; (iii) and then a Dexter energy transfer to phosphors. The requirement is that S1 should lie slightly lower than or close to T2 and twice as high as T1 in energy. For this, a scenario is put forward to design a series of donor-bridge-acceptor (DBA) type molecules with 2E(T1) ≤ E(S1) < E(T2), in which the Baird-type aromatic pyrazoline ring is used as a bridge owing to its stabilized T1 (1.30–1.74 eV) and different kinds of donors and acceptors are linked to the bridge for regulating S1 (2.35–3.87 eV) and T2 (2.44–3.96 eV). The ultrafast spectroscopy and sensitization measurements for one compound (TPA-DBPrz) fully confirm the theoretical predictions.

Graphical abstract: Molecular design of DBA-type five-membered heterocyclic rings to achieve 200% exciton utilization for electroluminescence

Supplementary files

Article information

Article type
Communication
Submitted
22 Jul 2022
Accepted
06 Sep 2022
First published
08 Sep 2022

Mater. Horiz., 2022,9, 2518-2523

Molecular design of DBA-type five-membered heterocyclic rings to achieve 200% exciton utilization for electroluminescence

Q. Sun, Y. Wu, Y. Cui, C. Gao, Q. Ou, D. Hu, L. Wang, Y. Wang, H. Dong, J. Zhao, C. Zhang, Z. Shuai, H. Fu and Q. Peng, Mater. Horiz., 2022, 9, 2518 DOI: 10.1039/D2MH00919F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements