High stability light-emitting electrochemical cells from cationic iridium complexes with bulky 5,5′ substituents

被引:51
|
作者
Sun, Liangfeng [2 ]
Galan, Armand [3 ]
Ladouceur, Sebastien [4 ]
Slinker, Jason D. [1 ]
Zysman-Colman, Eli [4 ]
机构
[1] Univ Texas Dallas, Dept Phys, Richardson, TX 75080 USA
[2] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
[3] Cornell Univ, Dept Mat Sci & Engn, Ithaca, NY 14853 USA
[4] Univ Sherbrooke, Dept Chim, Sherbrooke, PQ J1K 2R1, Canada
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
ELECTROLUMINESCENT DEVICES; PHOTOPHYSICAL PROPERTIES; SINGLE-LAYER; EFFICIENT; GREEN; REDUCTION; REDOX;
D O I
10.1039/c1jm12984h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We explore the photophysical, electrochemical, and electroluminescent properties of the ionic transition metal complex [(ppy)(2)Ir(bpy*)](PF6) where ppyH is 2-phenylpyridine and bpy* is 5,5'-diaryl-2,2'-bipyridine. Single layer devices of the structure ITO/[(ppy)(2)Ir(bpy*)](PF6)/Au exhibited high stability, with half-lives on the order of 100 h at a bias of -4 V. Long lifetimes are achieved through the bulky nature of the aryl substituents, which serves to limit chromophore-chromophore self-quenching, and 5,5' positioning of these bulky groups is clearly advantageous for device performance.
引用
收藏
页码:18083 / 18088
页数:6
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