4.6 Article

Theoretical Design of Blue-Color Phosphorescent Complexes for Organic Light-Emitting Diodes: Emission Intensities and Nonradiative Transition Rate Constants in Ir(ppy)2(acac) Derivatives

期刊

JOURNAL OF PHYSICAL CHEMISTRY A
卷 125, 期 50, 页码 10604-10614

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpca.1c08261

关键词

-

资金

  1. Ministry of Education, Culture, Sport, Science and Technology (MEXT) in Japan [JP20H02716, JP19K05375, JP21H04564]

向作者/读者索取更多资源

Theoretical calculations were conducted to determine the best candidate for a blue-color phosphorescent complex among several derivatives of bis(2-phenylpyridine)(acetylacetonate)iridium(III). Results showed that the introduction of F and/or CN substituents in certain positions of the ligands causes a blue shift of emission spectra, with Ir(5CN,6-F-ppy)2(acac) being identified as a promising candidate due to its calculated rate constants for S1 -Aa T1 and moderate emission intensity.
Theoretical calculations of phosphorescent spectra and nonradiative transition (NRT) rate constants for S1 -Aa T1, T1 -Aa S0, and S1 -Aa S0 were carried out to determine the best candidate for a blue-color phosphorescent complex among several derivatives of bis(2-phenylpyridine)(acetylacetonate)iridium(III). The geometries of the ground state (S0), the lowest triplet state (T1), and the lowest excited singlet state (S1) were optimized at the levels of density functional theory, in which B3LYP functionals and SBKJC+p basis sets were used. The NRT rate constants were derived by using a generating function method within the displaced harmonic oscillator model. The results of the calculation for phosphorescence showed that the introduction of F and/or CN substituents at the 4 '/6 '-th and 5 '-th sites in 2-phenylpyridinate (ppy) ligands, respectively, causes a blue shift of the emission spectra. They also suggest that Ir(5CN,6-F-ppy)2(acac), denoted 3(56) in the text, is a good candidate for a blue-color phosphorescent complex because a blue shift of emission spectra and a moderate intensity are obtained for phosphorescence and, furthermore, this complex is calculated to have a large rate constant for S1 -Aa T1 and relatively smaller rate constants for T1 -Aa S0 and S1 -Aa S0 based on the calculations of spin-orbit coupling and nonadiabatic coupling constants.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据