Fabrication of efficient light-emitting electrochemical cells utilizing thiazole- and pyridine-based cationic iridium complexes

被引:6
|
作者
Jeon, Youngbae [1 ]
Sunesh, Chozhidakath Damodharan [1 ]
Chitumalla, Ramesh Kumar [2 ]
Jang, Joonkyung [2 ]
Choe, Youngson [1 ]
机构
[1] Pusan Natl Univ, Dept Polymer Sci & Chem Engn, Busan 609735, South Korea
[2] Pusan Natl Univ, Dept Nanoenergy Engn, Busan 609735, South Korea
基金
新加坡国家研究基金会;
关键词
Light-emitting electrochemical cells; Iridium complexes; DFT calculations; Thiazole; Benzimidazole; EFFECTIVE CORE POTENTIALS; DENSITY-FUNCTIONAL THERMOCHEMISTRY; AB-INITIO; ELECTROLUMINESCENT PROPERTIES; MOLECULAR CALCULATIONS; BLUE-GREEN; IONIC LIQUIDS; SINGLE-LAYER; DEVICES; RUTHENIUM(II);
D O I
10.1016/j.electacta.2016.02.138
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this paper, we report highly luminescent yellow and orange light-emitting electrochemical cells (LECs) using cationic iridium complexes, i.e., [Ir(ppy)(2)(mpbi)]PF6 (Complex 1) and [Ir(bpbt)(2)(mpbi)]PF6 (Complex 2), which contain 2-phenylpyridine (ppy) and 2-(4-bromophenyl)benzothiazole (bpbt) as the cyclometalating ligands, respectively, and 2-(4-methyl-2-pyridyl)-1H-benzimidazole (mpbi) as the ancillary ligand. The emissions of Complex 1 and Complex 2 are yellow and yellowish-green in acetonitrile solution. The geometrical, electronic, and optical properties of the two novel Ir complexes were investigated by density functional theory (DFT) and time-dependent DFT using the B3LYP method. LECs incorporating Complexes 1 and 2 emit yellow (553 nm) and orange (600 nm) electroluminescence, respectively. Upon the meticulous selection of organic ligands, a significant increase in luminescence was achieved for Complex 1 (3636 cd/m(2)) over that of Complex 2 (2315 cd/m(2)). (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:112 / 123
页数:12
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