Charge-transfer transition regulation of thermally activated delayed fluorescence emitters by changing the valence of sulfur atoms

2020 ◽  
Vol 8 (48) ◽  
pp. 17457-17463
Author(s):  
Xiang Zhang ◽  
Jia-Xiong Chen ◽  
Kai Wang ◽  
Yi-Zhong Shi ◽  
Xiao-Chun Fan ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Sulfur Atom ◽  
Delayed Fluorescence ◽  
Charge Transfer Transition ◽  
Thermally Activated Delayed Fluorescence ◽  
Thermally Activated ◽  
Charge Transfer Transitions

Changing the valence of a sulfur atom to form two novel thermally activated delayed fluorescence emitters with different charge transfer transitions.

scholarly journals Solution-Processed OLEDs Based on Thermally Activated Delayed Fluorescence Copper(I) Complexes with Intraligand Charge-Transfer Excited State

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 1125
Author(s):  
Teng Teng ◽  
Jinfan Xiong ◽  
Gang Cheng ◽  
Changjiang Zhou ◽  
Xialei Lv ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Density Functional ◽  
Delayed Fluorescence ◽  
Quantum Yields ◽  
Functional Theory ◽  
Solution Processed ◽  
Thermally Activated Delayed Fluorescence ◽  
Light Emitting ◽  
Thermally Activated ◽  
Wide Range

A new series of tetrahedral heteroleptic copper(I) complexes exhibiting efficient thermally-activated delayed fluorescence (TADF) in green to orange electromagnetic spectral regions has been developed by using D-A type N^N ligand and P^P ligands. Their structures, electrochemical, photophysical, and electroluminescence properties have been characterized. The complexes exhibit high photoluminescence quantum yields (PLQYs) of up to 0.71 at room temperature in doped film and the lifetimes are in a wide range of 4.3–24.1 μs. Density functional theory (DFT) calculations on the complexes reveal the lowest-lying intraligand charge-transfer excited states that are localized on the N^N ligands. Solution-processed organic light emitting diodes (OLEDs) based on one of the new emitters show a maximum external quantum efficiency (EQE) of 7.96%.

High efficient T-shape deep-red thermally activated delayed fluorescence emitter: substitution position effect

2021 ◽  
Author(s):  
Kai Zhang ◽  
Jianzhong Fan ◽  
Chuankui Wang ◽  
Lili Lin
Keyword(s):  
Charge Transfer ◽  
Position Effect ◽  
Luminescent Properties ◽  
Delayed Fluorescence ◽  
Molecular Structures ◽  
Transfer Property ◽  
Thermally Activated Delayed Fluorescence ◽  
Thermally Activated ◽  
High Efficient ◽  
The Relationship

Modulating the relationship between molecular structures and luminescent properties as well as the charge transfer property for deep-red thermally activated delayed fluorescence (TADF) emitters has always been a powerful challenge,...

Blue Thermally Activated Delayed Fluorescence Polymers with Nonconjugated Backbone and Through-Space Charge Transfer Effect

2017 ◽  
Vol 139 (49) ◽  
pp. 17739-17742 ◽  
Author(s):  
Shiyang Shao ◽  
Jun Hu ◽  
Xingdong Wang ◽  
Lixiang Wang ◽  
Xiabin Jing ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Space Charge ◽  
Transfer Effect ◽  
Delayed Fluorescence ◽  
Thermally Activated Delayed Fluorescence ◽  
Thermally Activated

scholarly journals Synthesis and optoelectronic properties of benzoquinone-based donor–acceptor compounds

2019 ◽  
Vol 15 ◽  
pp. 2914-2921
Author(s):  
Daniel R Sutherland ◽  
Nidhi Sharma ◽  
Georgina M Rosair ◽  
Ifor D W Samuel ◽  
Ai-Lan Lee ◽  
...  
Keyword(s):  
Charge Transfer ◽  
Delayed Fluorescence ◽  
Optoelectronic Properties ◽  
Donor Group ◽  
Thermally Activated Delayed Fluorescence ◽  
Thermally Activated ◽  
Palladium Catalyzed ◽  
Donor Acceptor

Herein, we report a mild and efficient palladium-catalyzed C–H functionalization method to synthesize a series of benzoquinone (BQ)-based charge-transfer (CT) derivatives in good yields. The optoelectronic properties of these compounds were explored both theoretically and experimentally and correlations to their structures were identified as a function of the nature and position of the donor group (meta and para) attached to the benzoquinone acceptor. Compound 3, where benzoquinone is para-conjugated to the diphenylamine donor group, exhibited thermally activated delayed fluorescence (TADF) with a biexponential lifetime characterized by a prompt ns component and a delayed component of 353 μs.

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