有机发光二极管
量子产额
电致发光
卡宾
材料科学
激发态
量子效率
光致发光
金属
光化学
配体(生物化学)
酰胺
荧光
光电子学
化学
纳米技术
光学
原子物理学
物理
有机化学
冶金
受体
催化作用
生物化学
图层(电子)
作者
Ao Ying,Yu‐Hsin Huang,Chen‐Han Lu,Zhanxiang Chen,Wei‐Kai Lee,Xuan Zeng,Tianhao Chen,Xiaosong Cao,Chung‐Chih Wu,Shaolong Gong,Chuluo Yang
标识
DOI:10.1021/acsami.0c22109
摘要
How to develop efficient red-emitting organometallics of earth-abundant copper(I) is a formidable challenge in the field of organic light-emitting diodes (OLEDs) because Cu(I) complexes have weak spin-orbit coupling and a serious excited-state reorganization effect. Here, a red Cu(I) complex, MAC*-Cu-DPAC, was developed using a rigid 9,9-diphenyl-9,10-dihydroacridine donor ligand in a carbene-metal-amide motif. The Cu(I) complex achieved satisfactory red emission, a high photoluminescence quantum yield of up to 70%, and a sub-microsecond lifetime. Thanks to a linear geometry and the acceptor and donor ligands in a coplanar conformation, the complex exhibited a high horizontal dipole ratio of 77% in the host matrix, first demonstrated for coinage metal(I) complexes. The resulting OLEDs delivered high external quantum efficiencies of 21.1% at a maximum and 20.1% at 1000 nits, together with a red emission peak at ∼630 nm. These values represent the state-of-the-art performance for red-emitting OLEDs based on coinage metal complexes.
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