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  4. Homoleptic Ir(III) Phosphors with 2-Phenyl-1,2,4-triazol-3-ylidene Chelates for Efficient Blue Organic Light-Emitting Diodes
 
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Homoleptic Ir(III) Phosphors with 2-Phenyl-1,2,4-triazol-3-ylidene Chelates for Efficient Blue Organic Light-Emitting Diodes

Journal
ACS Applied Materials and Interfaces
Journal Volume
13
Journal Issue
49
Pages
59023-59034
Date Issued
2021
Author(s)
You C
Wang X.-Q
Zhou X
Yuan Y
Liao L.-S
Liao Y.-C
PI-TAI CHOU  
Chi Y.
DOI
10.1021/acsami.1c17308
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85120869221&doi=10.1021%2facsami.1c17308&partnerID=40&md5=f848363cc611b51a00da4f5d2842fe6a
https://scholars.lib.ntu.edu.tw/handle/123456789/626291
Abstract
In this report, we synthesized two series of deep-blue-emitting homoleptic iridium(III) phosphors bearing 1,2,4-triazol-3-ylidene and 5-(trifluoromethyl)-1,2,4-triazol-3-ylidene cyclometalate. Compared with reported synthetic routes using Ag2O as the promoter, herein, we adopted a different strategy to furnish these complexes in high yields. Also, the meridional to facial isomerization was executed in the presence of trifluoroacetic acid. These phosphors were examined using NMR spectroscopies, single-crystal X-ray diffraction studies, and photophysical methods. The results revealed that electron-withdrawing trifluoromethyl substitution on the N-heterocyclic carbene fragment only gave a minor variation of photoluminescence peak wavelengths and a decrease in radiative lifetime but notable reduction in thermal stabilities. The parent 1,2,4-triazol-3-ylidene complexes have been demonstrated to be suitable for use as deep-blue phosphors, with structured emission with the peak max. located at ∼420 nm and with photoluminescence quantum yields in a range of 34.8-42.5% in degassed THF solution at RT. Fabrication of both the phosphorescent organic light-emitting diodes (OLEDs) and phosphor-sensitized OLEDs (or hyperphosphorescence) was successfully conducted, from which the OLED device based on m-tz1 showed a max. external quantum efficiency (EQE) of 10% with CIEx,y coordinates of 0.15, 0.06, while the corresponding hyperphosphorescent OLED using m-tz2 as a sensitizer and t-DABNA as a terminal emitter afforded a significantly improved max. EQE of 19.7%, EL λmax of 468 nm, and FWHM of 31 nm with CIEx,y coordinates of 0.12, 0.13. ©
Subjects
carbene; cyclometalate; hyperphosphorescence; iridium; triazole; triazolylidene
SDGs

[SDGs]SDG6

[SDGs]SDG7

Other Subjects
Iridium compounds; Nuclear magnetic resonance spectroscopy; Organic light emitting diodes (OLED); Phosphorescence; Photoluminescence; Quantum efficiency; Silver oxides; Single crystals; Supercomputers; X ray diffraction; Blue organic light emitting diodes; Carbenes; Cyclometalate; Deep blue; External quantum efficiency; Homoleptic; Hyperphosphorescence; Triazole; Triazolylidene; Trifluoromethyl; Organic compounds
Type
journal article

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