Phosphorescent Carbene-Gold-Arylacetylide Materials as Emitters for Near UV-OLEDs.
Phosphorescent Carbene-Gold-Arylacetylide Materials as Emitters for Near UV-OLEDs.
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磷光卡宾-金-芳基乙炔材料作为近紫外 OLED 的发射体。
DOI:
10.1002/adma.202306249
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发表时间:
2024
期刊:
影响因子:
--
通讯作者:
Brannan AC
中科院分区:
文献类型:
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作者:
Brannan AC
A series of carbene‐gold‐acetylide complexes [(BiCAAC)AuCC]nC6H5−n(n= 1,Au1;n= 2,Au2;n= 3,Au3; BiCAAC = bicyclic(alkyl)(amino)carbene) have been synthesized in high yields. CompoundsAu1–Au3exhibit deep‐blue to blue‐green phosphorescence with good quantum yields up to 43% in all media. An increase of the (BiCAAC)Au moieties in gold complexesAu1–Au3increases the extinction coefficients in the UV–vis spectra and stronger oscillator strength coefficients supported by theoretical calculations. The luminescence radiative rates decrease with an increase of the (BiCAAC)Au moieties. The time‐dependent density functional theory study supports a charge‐transfer nature of the phosphorescence due to the large (0.5–0.6 eV) energy gap between singlet excited (S1) and triplet excited (T1) states. Transient luminescence study reveals the presence of both nonstructured UV prompt‐fluorescence and vibronically resolved long‐lived phosphorescence 428 nm. Organic light‐emitting diodes (OLED) are fabricated by physical vapor deposition with 2,8‐bis(diphenylphosphoryl)dibenzo[b,d]furan (PPF) as a host material with complexAu1. The near‐UV electroluminescence is observed at 405 nm with device efficiency of 1% while demonstrating OLED device lifetime LT50up to 20 min at practical brightness of 10 nits, indicating a highly promising class of materials to develop stable UV‐OLEDs.