scholarly journals Protonation-Induced Fluorescence Modulation of Carbazole-Based Emitters

2022 ◽  
Author(s):  
Essi Taipale ◽  
Nikita Durandin ◽  
Jaganish Salunke ◽  
Nuno R. Candeias ◽  
Tero-Petri Ruoko ◽  
...  
Keyword(s):  
High Efficiency ◽  
Light Emitting Diodes ◽  
Organic Light Emitting Diodes ◽  
Light Emitting ◽  
Thermally Activated ◽  
Organic Light ◽  
Fluorescence Modulation

The development of high-efficiency organic light-emitting diodes is of great importance for the growing lighting and display technologies. A potential way of responding to this demand is thermally activated delayed...

scholarly journals High efficiency blue organic light-emitting diodes with below-bandgap electroluminescence

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Maria Vasilopoulou ◽  
Abd. Rashid bin Mohd Yusoff ◽  
Matyas Daboczi ◽  
Julio Conforto ◽  
Anderson Emanuel Ximim Gavim ◽  
...  
Keyword(s):  
High Efficiency ◽  
Light Emitting Diodes ◽  
High Mobility ◽  
Organic Light Emitting Diodes ◽  
Triplet Energy ◽  
Material Interface ◽  
Light Emitting ◽  
Thermally Activated ◽  
Organic Light ◽  
Hole Transporting

AbstractBlue organic light-emitting diodes require high triplet interlayer materials, which induce large energetic barriers at the interfaces resulting in high device voltages and reduced efficiencies. Here, we alleviate this issue by designing a low triplet energy hole transporting interlayer with high mobility, combined with an interface exciplex that confines excitons at the emissive layer/electron transporting material interface. As a result, blue thermally activated delay fluorescent organic light-emitting diodes with a below-bandgap turn-on voltage of 2.5 V and an external quantum efficiency (EQE) of 41.2% were successfully fabricated. These devices also showed suppressed efficiency roll-off maintaining an EQE of 34.8% at 1000 cd m−2. Our approach paves the way for further progress through exploring alternative device engineering approaches instead of only focusing on the demanding synthesis of organic compounds with complex structures.

Spatially optimized quaternary phosphine oxide host materials for high-efficiency blue phosphorescence and thermally activated delayed fluorescence organic light-emitting diodes

2015 ◽  
Vol 3 (43) ◽  
pp. 11385-11396 ◽  
Author(s):  
Dongxue Ding ◽  
Zhen Zhang ◽  
Ying Wei ◽  
Pengfei Yan ◽  
Hui Xu
Keyword(s):  
Phosphine Oxide ◽  
High Efficiency ◽  
Light Emitting Diodes ◽  
Spatial Optimization ◽  
Delayed Fluorescence ◽  
Organic Light Emitting Diodes ◽  
Light Emitting ◽  
Thermally Activated ◽  
Organic Light ◽  
Host Materials

Spatial optimization of host materials for highly efficient blue organic light-emitting diodes was rationally performed on the basis of a series of ternary and quaternary phosphine oxide materials.

High efficiency above 20% in polymeric thermally activated delayed fluorescent organic light-emitting diodes by a host embedded backbone structure

2019 ◽  
Vol 10 (35) ◽  
pp. 4872-4878 ◽  
Author(s):  
Yun Hwan Park ◽  
Ho Jin Jang ◽  
Jun Yeob Lee
Keyword(s):  
High Efficiency ◽  
Light Emitting Diodes ◽  
Light Emitting Diode ◽  
Organic Light Emitting Diodes ◽  
Light Emitting ◽  
Organic Light Emitting Diode ◽  
Thermally Activated ◽  
Highly Efficient ◽  
Organic Light ◽  
Backbone Structure

A highly efficient polymeric thermally activated delayed fluorescent (TADF) organic light-emitting diode was developed by synthesizing a copolymer with 9-vinylcarbazole (VCz) and TADF repeating units.

Design of thermally activated delayed fluorescent sensitizers for high efficiency over 20% and long lifetime in yellow fluorescent organic light-emitting diodes

2020 ◽  
Vol 8 (15) ◽  
pp. 5265-5272 ◽  
Author(s):  
Ji Han Kim ◽  
Kyung Hyung Lee ◽  
Jun Yeob Lee
Keyword(s):  
High Efficiency ◽  
Light Emitting Diodes ◽  
Delayed Fluorescence ◽  
Organic Light Emitting Diodes ◽  
Thermally Activated Delayed Fluorescence ◽  
Light Emitting ◽  
Thermally Activated ◽  
Organic Light ◽  
Long Lifetime

Yellow thermally activated delayed fluorescence materials were synthesized using two types of acceptors of 2,4,6-triphenylpyrimidine-5-carbonitrile and 4-(3-cyanophenyl)-2,6-diphenylpyrimidine-5-carbonitrile combined with a strong donor.

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