Issue 15, 2024

Efficient narrowband bluish-green emitters derived from a double-carbazole-fused organoboron multiple resonance skeleton with internal-structure modification

Abstract

The double-carbazole-fused organoboron framework CzBN is a widely used parent skeleton in designs of multiple resonance (MR) emitters. Currently, the majority of CzBN derivatives are derived from peripheral modification strategies. Here, we focus on internal-structure modification of the CzBN skeleton and thus develop two narrowband bluish-green MR emitters by directly embedding thiophene units into the CzBN skeleton. This incorporation of thiophene units not only extends the π-conjugated backbone towards red-shifted emission, but also improves the MR characteristics and structural rigidity for narrowband features. Both emitters achieve narrowband bluish-green emissions with extremely small full width at half maximum of ca. 23 nm in dilute toluene. Moreover, the optimized sensitized device based on BTPCzBN as the terminal emitter achieves a high maximum external quantum efficiency of up to 24% with suppressed efficiency roll-off. This work not only presents a distinct strategy for the development of CzBN derivatives via internal-structure modification of MR skeletons, but also provides valuable inspiration for the design of heteroatom-fused narrowband emitters.

Graphical abstract: Efficient narrowband bluish-green emitters derived from a double-carbazole-fused organoboron multiple resonance skeleton with internal-structure modification

Supplementary files

Article information

Article type
Paper
Submitted
12 جمادى الثانية 1445
Accepted
05 رمضان 1445
First published
08 رمضان 1445

J. Mater. Chem. C, 2024,12, 5386-5392

Efficient narrowband bluish-green emitters derived from a double-carbazole-fused organoboron multiple resonance skeleton with internal-structure modification

T. Zhang, Y. Cheng, H. Wang, F. Huang, X. Xiong, X. Fan, J. Yu, K. Wang and X. Zhang, J. Mater. Chem. C, 2024, 12, 5386 DOI: 10.1039/D3TC04771G

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