Autor: |
Zijian Chen, Mengke Li, Qing Gu, Xiaomei Peng, Weidong Qiu, Wentao Xie, Denghui Liu, Yihang Jiao, Kunkun Liu, Jiadong Zhou, Shi‐Jian Su |
Jazyk: |
angličtina |
Rok vydání: |
2023 |
Předmět: |
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Zdroj: |
Advanced Science, Vol 10, Iss 12, Pp n/a-n/a (2023) |
Druh dokumentu: |
article |
ISSN: |
2198-3844 |
DOI: |
10.1002/advs.202207003 |
Popis: |
Abstract Purely organic room‐temperature phosphorescence (RTP) materials generally exhibit low phosphorescence quantum yield (ϕP) and long phosphorescence lifetime (τP) due to the theoretically spin‐forbidden triplet state. Herein, by introducing a donor–acceptor (D–A) skeleton with a phenoxaselenine donor, three nonaromatic amine donor containing compounds with high ϕP and short τP in amorphous films are developed. Besides the enhanced spin–orbit coupling (SOC) by the heavy‐atom effect of selenium, the D–A skeleton which facilitates orbital angular momentum change can further boost SOC, and severe nonradiative energy dissipation is also suppressed by the rigid molecular structure. Consequently, a record‐high external quantum efficiency of 19.5% are achieved for the RTP organic light‐emitting diode (OLED) based on 2‐(phenoxaselenin‐3‐yl)‐4,6‐diphenyl‐1,3,5‐triazine (PXSeDRZ). Moreover, voltage‐dependent color‐tunable emission and single‐molecule white emission are also realized. These results shed light on the broad prospects of purely organic phosphorescence materials as highly efficient OLED emitters especially for potential charming lighting applications. |
Databáze: |
Directory of Open Access Journals |
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