Yellowish-orange and red emitting quinoline-based iridium(III) complexes: Synthesis, thermal, optical and electrochemical properties and OLED application


Altinolcek N., Battal A., TAVASLI M., Cameron J., Peveler W. J., Yu H. A., ...Daha Fazla

SYNTHETIC METALS, cilt.268, 2020 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 268
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1016/j.synthmet.2020.116504
  • Dergi Adı: SYNTHETIC METALS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, PASCAL, Aerospace Database, Chimica, Communication Abstracts, Compendex, INSPEC, Metadex, Civil Engineering Abstracts
  • Anahtar Kelimeler: Formyl group, 2-Phenylquinoline, Iridium, Heteroleptic, Phosphorescence, Electroluminescence, EXTERNAL QUANTUM EFFICIENCY, HIGHLY EFFICIENT, PHOTOPHYSICAL PROPERTIES, DEEP-RED, ENERGY-TRANSFER, DIODES, LIGANDS, COLOR, EMISSION, 2-PHENYLPYRIDINE
  • Bursa Uludağ Üniversitesi Adresli: Evet

Özet

Two novel heteroleptic iridium(III) acetylacetonate (acac) complexes K3a and K3b were synthesised from cyclometallating ligands of 2-(4'-formylphenyl)quinoline lla and 2-(5'-formylphenyl)quinoline 11b. Complexes K3a and K3b were fully characterised by NMR spectroscopy, mass spectrometry and FT-IR. Differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA) indicate that both complexes were amorphous solids, stable up to 303 degrees C and 313 degrees C, respectively. Complexes K3a and K3b showed strong, high-energy absorption bands ( <400 nm) due to ligand-centred ((LC)-L-1) transitions and weaker, low-energy absorption bands (400 - 600 nm) arising from a mixture of metal-to-ligand charge transfer ((MLCT)-M-1/(MLCT)-M-3) and ligand-centred ((LC)-L-3) transitions. In degassed dichloromethane solutions, complexes K3a and K3b gave yellowish-orange and red phosphorescent emissions at 579 nm and 630 nm, with quantum efficiencies of 99.3 % and 79.3 %, respectively. At positive potential, complexes K3a and K3b exhibited a one-electron reversible oxidation (En) peak at 0.69 V and a quasi-reversible oxidation (ET1/2ox) peak at 0.60 V, respectively, which were assigned to the Ir (III)/Ir(IV) couple. At negative potentials, complexes K3a and K3b exhibited a one-electron irreversible reduction peak at -1.79 V and -1.94 V, respectively. Phosphorescent organic light-emitting diodes (PhOLEDs) were fabricated with a device configuration of ITO/PEDOT:PSS/EML/TPBi/LiF/Al, in which K3a and K3b gave yellowish-orange and red electroluminescence (EL) at 572 nm and 628 nm, respectively. Complex K3a gave the highest luminance of 2773 cd/m(2), current efficiency of 3.3 cd/A, external quantum efficiency of 1.2 % and maximum power efficiency of 1.05 lm/W with a turn-on voltage of 5.0 V (Device A).