Archetype Cationic Iridium Complexes and Their Use in Solid-State Light-Emitting Electrochemical Cells

被引:240
作者
Costa, Ruben D. [1 ]
Orti, Enrique [1 ]
Bolink, Henk J. [1 ,2 ]
Graber, Stefan [3 ]
Schaffner, Silvia [3 ]
Neuburger, Markus [3 ]
Housecroft, Catherine E. [3 ]
Constable, Edwin C. [3 ]
机构
[1] Univ Valencia, Inst Ciencia Mol, Valencia, Spain
[2] FGUV, Valencia, Spain
[3] Univ Basel, Dept Chem, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
FUNCTIONAL RESPONSE THEORY; ELECTROLUMINESCENT DEVICES; EXCITATION-ENERGIES; SUBSTITUENTS; SPECTRA; IR(III); BLUE;
D O I
10.1002/adfm.200900911
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The archetype ionic transition-metal complexes (iTMCs) [Ir(ppy)(2)(bpy)][PF6] and [Ir(ppy)(2)(phen)][PF6], where Hppy = 2-phenylpyridine, bpy = 2,2'-bipyridine, and phen = 1,1 0-phenanthroline, are used as the primary active components in light-emitting electrochemical cells (LECs). Solution and solid-state photophysical properties are reported for both complexes and are interpreted with the help of density functional theory calculations. LEC devices based on these archetype complexes exhibit long turn-on times (70 and 160h, respectively) and low external quantum efficiencies (similar to 2%) when the complex is used as a pure film. The long turn-on times are attributed to the low mobility of the counterions. The performance of the devices dramatically improves when small amounts of ionic liquids (ILs) are added to the Ir-iTMC: the turn-on time improves drastically (from hours to minutes) and the device current and power efficiency increase by almost one order of magnitude. However, the improvement of the turn-on time is unfortunately accompanied by a decrease in the stability of the device from 700 h to a few hours. After a careful study of the Ir-iTMC:IL molar ratios, an optimum between turn-on time and stability is found at a ratio of 4:1. The performance of the optimized devices using these rather simple complexes is among the best reported to date. This holds great promise for devices that use specially-designed iTMCs and demonstrates the prospect for LECs as low-cost light sources.
引用
收藏
页码:3456 / 3463
页数:8
相关论文
共 45 条
[21]   Stability of thin-film solid-state electroluminescent devices based on tris(2,2′-bipyridine)ruthenium(II) complexes [J].
Kalyuzhny, G ;
Buda, M ;
McNeill, J ;
Barbara, P ;
Bard, AJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (20) :6272-6283
[22]   Efficient electrogenerated chemiluminescence from cyclometalated iridium(III) complexes [J].
Kim, JI ;
Shin, IS ;
Kim, H ;
Lee, JK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (06) :1614-1615
[23]   DEVELOPMENT OF THE COLLE-SALVETTI CORRELATION-ENERGY FORMULA INTO A FUNCTIONAL OF THE ELECTRON-DENSITY [J].
LEE, CT ;
YANG, WT ;
PARR, RG .
PHYSICAL REVIEW B, 1988, 37 (02) :785-789
[24]   Synthesis, structure, and photophysical and electrochemical properties of cyclometallated iridium(III) complexes with phenylated bipyridine ligands [J].
Lepeltier, M ;
Lee, TKM ;
Lo, KKW ;
Toupet, L ;
Le Bozec, H ;
Guerchais, W .
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2005, (01) :110-117
[25]   Accelerated luminophore discovery through combinatorial synthesis [J].
Lowry, MS ;
Hudson, WR ;
Pascal, RA ;
Bernhard, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (43) :14129-14135
[26]   Theoretical studies of phosphorescence spectra of tris( 2,2′-bipyridine) transition metal compounds [J].
Nozaki, Koichi ;
Takamori, Keisei ;
Nakatsugawa, Yuji ;
Ohno, Takeshi .
INORGANIC CHEMISTRY, 2006, 45 (16) :6161-6178
[27]  
OKADA H, 2002, Patent No. 2002203681
[28]   Processing of X-ray diffraction data collected in oscillation mode [J].
Otwinowski, Z ;
Minor, W .
MACROMOLECULAR CRYSTALLOGRAPHY, PT A, 1997, 276 :307-326
[29]   Improved turn-on times of iridium electroluminescent devices by use of ionic liquids [J].
Parker, ST ;
Slinker, JD ;
Lowry, MS ;
Cox, MP ;
Bernhard, S ;
Malliaras, GG .
CHEMISTRY OF MATERIALS, 2005, 17 (12) :3187-3190
[30]  
PEI Q, 2006, ADV MATER, V18, P1313