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Efficient near-infrared (NIR) polymer light-emitting diode (PLED) based on the binuclear [(C∧N)2Ir-(bis-N∧O)-Ir(C∧N)2] complex with aggregation-induced phosphorescent enhancement (AIPE) character
被引:18
|作者:
He, Yani
[1
]
Fu, Guorui
[1
]
Li, Wentao
[1
]
Wang, Baowen
[1
]
Miao, Tiezheng
[1
]
Tan, Mingfeng
[1
]
Feng, Weixu
[2
]
Lu, Xingqiang
[1
]
机构:
[1] Northwest Univ, Shaanxi Key Lab Degradable Med Mat, Sch Chem Engn, Xian 710069, Shaanxi, Peoples R China
[2] Northwestern Polytech Univ, Sch Sci, Dept Appl Chem, Xian 710029, Shaanxi, Peoples R China
关键词:
Dinuclear Ir(III)-Complex;
Aggregation-induced phosphorescent enhancement;
NIR luminescence;
Polymer light-emitting diode;
HETEROLEPTIC IRIDIUM(III) COMPLEXES;
IR(III) COMPLEX;
EMISSION;
LIGANDS;
RED;
D O I:
10.1016/j.jlumin.2019.116847
中图分类号:
O43 [光学];
学科分类号:
070207 ;
0803 ;
摘要:
In this work, for the obtained NIR-emitting dinuclear [(iqbt)(2)Ir-L-n-Ir(iqbt)(2)] complexes (n = 1-3, 1-3; Hiqbt = 1-(benzo[b]-thiophen-2-yl)-isoquinoline) with the bridging linkages of three flexible bis-(NO)-O-boolean AND-Schiff-base ligands H2Ln, their obvious aggregation-induced phosphorescent enhancement (AIPE) behaviors in powder-form solid or MeCN-H2O mixture are observed, respectively. Moreover, based on the AIPE-switched NIR phosphorescence (Phi(em) = 0.11 and tau = 0.27 mu s) of the diiridium complex 1 without electron-donating substituents in the aggregation state, its solution-processed NIR-PLED is reliably realized, exhibiting the attractive electroluminescent performance with both eta(max)(EQE) = 1.08% and almost negligible efficiency-roll-off.
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