High‐Efficiency Ultraviolet Electroluminescence from Multi‐Resonance Phosphine Oxide Polycyclic Aromatics

Author:

Ma Peng1,Chen Yingying1,Man Yi1,Qi Quan1,Guo Yuanting1,Wang Huiqin1,Li Zhe1,Chang Peng1,Qu Chao1,Han Chunmiao1,Xu Hui1ORCID

Affiliation:

1. Key Laboratory of Functional Inorganic Material Chemistry Ministry of Education School of Chemistry and Materials Heilongjiang University Harbin Heilongjiang 150080 China

Abstract

AbstractEfficient ultraviolet (UV) electroluminescent materials remain a great challenge, since short peak wavelength <400 nm and narrow full width at half maximum (FWHM) <50 nm are simultaneously required. In this sense, multi‐resonance (MR) thermally activated delayed fluorescence (TADF) emitters featuring narrow‐band emissions hold the promise for UV applications. Herein, a novel MR‐TADF skeleton featuring carbazole‐phosphine oxide (P=O) fused aromatics is developed to construct the first two UV MR emitters named CzP2PO and tBCzP2PO. In addition to synergistic resonance effects of P=O and N atom, sp3‐hybrid P atom renders the curved polycyclic planes of CzP2PO and tBCzP2PO, giving rise to their narrowband UV emissions with peak wavelengths <390 nm and FWHM<35 nm. Besides configuration quasi‐planarization for radiation enhancement and quenching suppression, P=O moiety further enhances singlet‐triplet coupling to facilitate reverse intersystem crossing, resulting in the state‐of‐the‐art photoluminescence quantum yield of 62 % in tBCzP2PO doped films. As consequence, tBCzP2PO endowed its UV organic light‐emitting diodes with the peak at 382 nm and FWHM of 32 nm, and especially the record‐high external quantum efficiency (EQE) of 15.1 % among all kinds of UV devices. Our results demonstrate great potential of P=O based MR emitters in practical applications including optoelectronics, biology and medicine science.

Funder

Changjiang Scholar Program, Ministry of Education

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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