Highly Efficient Electrofluorescence Material Based on Pure Organic Phosphor Sensitization*.

energy levels energy transfer organic electroluminescence pure organic room-temperature phosphorescence sensitization

Journal

Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543

Informations de publication

Date de publication:
05 Jul 2021
Historique:
received: 07 04 2021
pubmed: 28 4 2021
medline: 28 4 2021
entrez: 27 4 2021
Statut: ppublish

Résumé

Pure organic room-temperature phosphorescence (RTP) materials are considered as potential candidates for replacing precious metal complexes to fabricate highly efficient organic light-emitting devices (OLEDs). However, applications of the reported RTP materials in OLEDs are seriously impeded by their low photoluminescence quantum yields (PLQYs) in a thin film state. To overcome these obstacles, we established a new strategy to construct highly efficient OLEDs based on a pure organic RTP material sensitized fluorescence emitter by selecting benzimidazole-triazine molecules (PIM-TRZ), 2,6-di(phenothiazinyl)naphthalene (β-DPTZN), and 5,6,11,12-tetraphenylnaphthacene (rubrene) as host, phosphor sensitizer, and fluorescent emitter, respectively. The perfect combination of host, phosphorescent sensitizer, and fluorescent emitter in the emitting layer ensure the outstanding performance of the devices with an external quantum efficiency (EQE) of 15.7 %.

Identifiants

pubmed: 33904242
doi: 10.1002/anie.202104755
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

15335-15339

Subventions

Organisme : Innovative Research Group Project of the National Natural Science Foundation of China
ID : 21935005

Informations de copyright

© 2021 Wiley-VCH GmbH.

Références

C. W. Tang, S. A. VanSlyke, Appl. Phys. Lett. 1987, 51, 913-915.
M. A. Baldo, D. F. O'Brien, Y. You, A. Shoustikov, S. Sibley, M. E. Thompson, S. R. Forrest, Nature 1998, 395, 151-154.
H. Uoyama, K. Goushi, K. Shizu, H. Nomura, C. Adachi, Nature 2012, 492, 234-238.
X. Ai, E. W. Evans, S. Dong, A. J. Gillett, H. Guo, Y. Chen, T. J. H. Hele, R. H. Friend, F. Li, Nature 2018, 563, 536-540.
W. Li, Y. Pan, R. Xiao, Q. Peng, S. Zhang, D. Ma, F. Li, F. Shen, Y. Wang, B. Yang, Y. Ma, Adv. Funct. Mater. 2014, 24, 1609-1614.
 
H. Wang, H. Shi, W. Ye, X. Yao, Q. Wang, C. Dong, W. Jia, H. Ma, S. Cai, K. Huang, L. Fu, Y. Zhang, J. Zhi, L. Gu, Y. Zhao, Z. An, W. Huang, Angew. Chem. Int. Ed. 2019, 58, 18776-18782;
Angew. Chem. 2019, 131, 18952-18958;
H. Thomas, D. L. Pastoetter, M. Gmelch, T. Achenbach, A. Schlögl, M. Louis, X. Feng, S. Reineke, Adv. Mater. 2020, 32, 2000880;
Q. Liao, Q. Gao, J. Wang, Y. Gong, Q. Peng, Y. Tian, Y. Fan, H. Guo, D. Ding, Q. Li, Z. Li, Angew. Chem. Int. Ed. 2020, 59, 9946-9951;
Angew. Chem. 2020, 132, 10032-10037;
X. Zhang, L. Du, W. Zhao, Z. Zhao, Y. Xiong, X. He, P. F. Gao, P. Alam, C. Wang, Z. Li, J. Leng, J. Liu, C. Zhou, J. W. Y. Lam, D. L. Phillips, G. Zhang, B. Z. Tang, Nat. Commun. 2019, 10, 5161;
X. Ma, J. Wang, H. Tian, Acc. Chem. Res. 2019, 52, 738-748;
H. Ma, Q. Peng, Z. An, W. Huang, Z. Shuai, J. Am. Chem. Soc. 2019, 141, 1010-1015;
C. Chen, Z. Chi , K. C. Chong, A. S. Batsanov, Z. Yang, Z. Mao, Z. Yang, B. Liu, Nat. Mater. 2021, 20, 175-180;
T. Wang, X. Su, X. Zhang, X. Nie, L. Huang, X. Zhang, X. Sun, Y. Luo, G. Zhang, Adv. Mater. 2019, 31, 1904273.
J. Wang, J. Liang, Y. Xu, B. Liang, J. Wei, C. Li, X. Mu, K. Ye, Y. Wang, J. Phys. Chem. Lett. 2019, 10, 5983-5988.
B. Liang, J. Wang, Z. Cheng, J. Wei, Y. Wang, J. Phys. Chem. Lett. 2019, 10, 2811-2816.
 
M. A. Baldo, M. E. Thompson, S. R. Forrest, Nature 2000, 403, 750-753;
G. Cheng, Y. Zhang, Y. Zhao, S. Liu, Y. Ma, Appl. Phys. Lett. 2006, 88, 083512;
L. Paterson, A. Mondal, P. Heimel, R. Lovrincic, F. May, C. Lennartz, D. Andrienko, Adv. Electron. Mater. 2019, 5, 1900646;
H.-G. Kim, H. Shin, Y. H. Ha, R. Kim, S.-K. Kwon, Y.-H. Kim, J.-J. Kim, ACS Appl. Mater. Interfaces 2019, 11, 26-30;
K. H. Lee, J. Y. Lee, J. Mater. Chem. C 2019, 7, 8562-8568;
J. Yao, S. Ying, Q. Sun, Y. Dai, X. Qiao, D. Yang, J. Chen, D. Ma, J. Mater. Chem. C 2019, 7, 11293-11302;
H.-G. Kim, K.-H. Kim, J.-J. Kim, Adv. Mater. 2017, 29, 1702159;
P. Heimel, A. Mondal, F. May, W. Kowalsky, C. Lennartz, D. Andrienko, R. Lovrincic, Nat. Commun. 2018, 9, 4990.
A. Burghart, L. H. Thoresen, J. Chen, K. Burgess, F. Bergströmb, L. B.-Å. Johansson, Chem. Commun. 2000, 2203-2204.
Z. An, C. Zheng, Y. Tao, R. Chen, H. Shi, T. Chen, Z. Wang, H. Li, R. Deng, X. Liu, W. Huang, Nat. Mater. 2015, 14, 685-690.
The CCDC numbers of crystal-EtOH and crystal-PE are 2063597 and 2063598, respectively.

Auteurs

Jiaxuan Wang (J)

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.

Baoyan Liang (B)

Jihua Laboratory, 28 Huandao South Road, Foshan, 528200, Guangdong Province, P. R. China.

Jinbei Wei (J)

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.

Zhiqiang Li (Z)

Jihua Laboratory, 28 Huandao South Road, Foshan, 528200, Guangdong Province, P. R. China.

Yincai Xu (Y)

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.

Tong Yang (T)

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.

Chenglong Li (C)

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.

Yue Wang (Y)

State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.
Jihua Laboratory, 28 Huandao South Road, Foshan, 528200, Guangdong Province, P. R. China.

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