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1.1 μm near-infrared electrophosphorescence from organic light-emitting diodes based on copper phthalocyanine

机译:基于铜酞菁的有机发光二极管发出的1.1μm近红外电致磷光

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摘要

We demonstrated near-infrared organic light-emitting devices employing copper phthalocyanine (CuPc) doped into 4,4'-N,N'-dicarbazole-biphenyl (CBP). Room-temperature electrophosphorescence was observed at about 1.1 μm due to transitions from the first excited triplet state to the singlet ground state (T_1-S_0) of CuPc. There existed very weak emission of CBP from undoped devices, and at lower doping concentrations (≤ 12 wt %) the driving voltages of doped devices were higher than that of undoped devices. The results indicated that Foerster [Ann. Physik. (Leipzig) 2, 55 (1948)] and Dexter [J. Chem. Phys. 21, 836 (1953)] energy transfers play a minor role in these devices, and direct charge trapping appears to be the dominant mechanism.
机译:我们展示了使用掺入4,4'-N,N'-二咔唑-联苯(CBP)中的酞菁铜(CuPc)的近红外有机发光器件。由于从CuPc的第一激发三重态到单重态基态(T_1-S_0)的转变,室温电致磷光约为1.1μm。未掺杂器件的CBP发射非常弱,并且在较低的掺杂浓度(≤12 wt%)下,掺杂器件的驱动电压要高于未掺杂器件的驱动电压。结果表明,Foerster [Ann。理疗。 (莱比锡)2,55(1948)]和德克斯特[J.化学物理21,836(1953)]能量转移在这些装置中起次要作用,而直接电荷俘获似乎是主要机制。

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