材料科学
有机发光二极管
量子效率
光电子学
轨道能级差
磷光
部分
光化学
掺杂剂
分子内力
分子轨道
兴奋剂
分子
化学
纳米技术
荧光
光学
物理
有机化学
图层(电子)
作者
Hongyang Zhang,Zhao Chen,Longzhi Zhu,Yongquan Wu,Yuqing Xu,Shuming Chen,Wai‐Yeung Wong
标识
DOI:10.1002/adom.202200111
摘要
Abstract Advances in achieving high external quantum efficiency (EQE) of near‐infrared (NIR) organic light‐emitting diodes (OLEDs) are lagging behind that of the visible‐light OLEDs, according to the energy gap law. Herein, two structurally simple NIR‐phosphorescent Ir(III) complexes, DTCNIr and PTCNIr, with the cyclometalated ligands functionalized by the 1‐phenylisoquinoline‐4‐carbonitrile moiety and thieno/benzo[ b ]thiophene moiety are handily accessed within three synthetic steps. The introduction of the cyano unit can significantly lower the lowest unoccupied molecular orbitals whereas incorporating the conjugated group can elevate the highest occupied molecular orbitals of the newly designed Ir(III) complexes. The intramolecular charge transfer (ICT) transitions are enhanced due to the increased donor–acceptor interaction inside the metallophosphor. As a result, the emissions are red‐shifted to the NIR region with fast radiative decay. A maximum external quantum efficiency (EQE) of 8.11% with the emission peak at 726 nm for DTCNIr and a maximum EQE of 6.39% with the emission peak at 763 nm for PTCNIr are achieved in the NIR OLEDs by using these Ir(III) materials as the dopant emitters, a champion efficiency in the Ir(III)‐based OLEDs with the emission peak exceeding 760 nm.
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