Affiliation:
1. Institute for Chemical and Bioengineering ETH Zürich Zürich 8093 Switzerland
2. Department of Chemistry KU Leuven Leuven 3001 Belgium
3. Laboratory for Inorganic Chemistry ETH Zürich Zürich 8093 Switzerland
Abstract
AbstractOrganic light‐emitting diodes (OLEDs) are emerging as one of the most promising candidates for next‐generation optoelectronics. However, most commercial OLED displays are fabricated using organometallic phosphors containing rare transition metals, such as Ir(III) and Pt(II). Recently, the development of efficient phosphorescent emitters based on abundant Au(III) is drawing considerable attention. Here, rational molecular design of a series of Au(III) organometallic complexes consisting of asymmetric C^C^N ligands and carbazole moieties functionalized by phenyl or mesityl groups is presented. The synthesized complexes exhibit shortened radiative lifetimes, and reach improved photoluminescence quantum yield, ηPL, of greater than 93% in thin films. Moreover, the asymmetric molecular design induces anisotropic emission with a high ratio of horizontally oriented transition dipole moment of up to 82% in host‐guest films. Accordingly, high‐performance OLED devices with record‐high external quantum efficiencies, ηext, and current efficiencies, ηCE, of up to 27% and 89 cd A−1, respectively, are demonstrated. It is believed that the molecular design of anisotropic Au(III) emitters will be greatly facilitated by the fundamental principles and theoretical analysis presented here.
Funder
European Research Council
Subject
Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献