电致发光
有机发光二极管
镧系元素
螯合作用
配体(生物化学)
材料科学
结晶学
化学
光化学
离子
无机化学
纳米技术
有机化学
生物化学
受体
图层(电子)
作者
Мarina A. Katkova,Anatoly P. Pushkarev,Tatyana V. Balashova,А. Н. Конев,Georgy K. Fukin,Sergey Yu. Ketkov,M.N. Bochkarev
摘要
New near-IR electroluminescent complexes of Pr3+, Nd3+, Ho3+, Er3+, Tm3+, Yb3+ with N,O-chelated ligands, Ln2(OON)6 (OON = 2-(2-benzoxyazol-2-yl)phenolate) and Ln2(SON)6 (SON = 2-(2-benzothiazol-2-yl)phenolate), were synthesized by the reaction of Ln[N(SiMe3)2]3 and the corresponding N,O-chelating ligand. X-Ray analysis for the Pr and Nd compounds reveals centrosymmetric dimeric structures of the complexes. The solid-state electronic absorption spectra and the electroluminescent spectra show long-wavelength 4f–4f transitions which provide potential use of the compounds as NIR emitting materials in organic light-emitting devices (OLEDs). When constructing OLEDs based on Ln2(OON)6 and Ln2(SON)6, the best results were achieved with the Nd3+ and Yb3+ complexes, where the NIR wall plug efficiency of the ITO/TPD/Ln-complex/BATH/Yb system is 0.82 and 1.22 mW W−1, respectively.
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