Isomeric Engineering of Dithieno[3,2-b:2',3'-d]thiophene Derivatives for Efficient Deep-Blue OLEDs

Abstract

Simultaneously achieving deep-blue luminescence and high device performance remains a significant challenge for blue fluorescent emitters. In this study, a series of blue fluorescent isomers based on dithieno[3,2-b:2',3'-d]thiophene (DTT) core are rationally designed and synthesized. When incorporated into undoped OLEDs, all emitters exhibite stable blue emission with excellent color stability (ΔCIE < 0.01), achieving a maximum external quantum efficiency (EQE) of 3.94% and CIE coordinates of (0.14, 0.09). In doped configurations, these materials demonstrate efficient deep-blue emission with a maximum EQE of 3.97% and CIE coordinates of (0.15, 0.08), closely matching the NTSC standard for deep-blue emission (CIEy ≤ 0.08). This work establishes isomer-engineered DTT derivatives as promising candidates for high-performance deep-blue OLEDs, highlighting their potential for display and lighting applications.

Supplementary files

Article information

Article type
Paper
Submitted
04 Feb 2026
Accepted
17 May 2026
First published
19 May 2026

J. Mater. Chem. C, 2026, Accepted Manuscript

Isomeric Engineering of Dithieno[3,2-b:2',3'-d]thiophene Derivatives for Efficient Deep-Blue OLEDs

Y. Hou, C. Xiao, R. Xu, Y. Hou, H. Cheng, B. Chen and H. Zhang, J. Mater. Chem. C, 2026, Accepted Manuscript , DOI: 10.1039/D6TC00368K

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