All-organic fast intersystem crossing assisted exciplexes exhibiting sub-microsecond thermally activated delayed fluorescence

Author(s):  
Kaspars Traskovskis ◽  
Armands Sebris ◽  
Irina Novosjolova ◽  
Maris Turks ◽  
Matas Guzauskas ◽  
...  

A novel strategy is presented towards acquisition of exciplex systems exhibiting thermally activated delayed fluorescence (TADF) with high reverse intersystem crossing (RISC) rate (exceeding 107 s-1). This approach involves constructing...

2019 ◽  
Vol 43 (15) ◽  
pp. 6032-6039
Author(s):  
Songyan Feng ◽  
Xugeng Guo ◽  
Jinglai Zhang

The present results reveal that the dominant charge transfer characteristics in the S1 and T1 states produce a small energy difference between the two states, and consequently an efficient reverse intersystem crossing process and a high fluorescence efficiency.


2018 ◽  
Vol 6 (20) ◽  
pp. 5363-5368 ◽  
Author(s):  
Ji Han Kim ◽  
Dong Ryun Lee ◽  
Si Hyun Han ◽  
Jun Yeob Lee

Highly efficient red thermally activated delayed fluorescence organic light-emitting diodes were developed using a reverse intersystem crossing activating host derived from phenylcarbazole and pyridofuropyridine.


2021 ◽  
Author(s):  
Leonardo Evaristo de Sousa ◽  
Piotr de Silva

One of the challenges in organic light emitting diodes research is finding ways to increase device efficiency by making use of the triplet excitons that are inevitably generated in the process of electroluminescence. One way to do so is by thermally activated delayed fluorescence, a process in which singlet excitons undergo up-conversion to singlet states, allowing them to relax radiatively. The discovery of this phenomenon has ensued a quest for new materials that are able to effectively take advantage of this mechanism. From a theoretical standpoint, this requires the capacity to estimate the rates of the various processes involved in the photophysics of candidate molecules, such as intersystem crossing, reverse intersystem crossing, fluorescence and phosphorescence. Here we present a method that is able to, within a single framework, compute all these rates and predict the photophysics of new molecules. We apply the method to two TADF molecules and show that results compare favorably with other theoretical approaches and experimental results. Finally, we use a kinetic model to show how the calculated rates act in concert to produce different photophysical behavior.


2021 ◽  
Author(s):  
A. Lennart Schleper ◽  
Kenichi Goushi ◽  
Christoph Bannwarth ◽  
Bastian Haehnle ◽  
Philipp Welscher ◽  
...  

Rapid reverse intersystem crossing and high color purity are vital characteristics of emitters with thermally activated delayed fluorescence in opto-electronic devices. We present a new approach, called “hot exciplexes” that enables access to both attributes at the same time. Hot exciplexes are produced by coupling facing donor and acceptor moieties to an anthracene bridge, yielding an exciplex with large T1 to T2 spacing. The hot exciplex model is investigated using optical spec-troscopy and quantum chemical simulations. Reverse intersystem crossing is found to occur preferentially from the T3 to the S1 state within only a few nanoseconds. Application and practi-cality of the model are shown by fabrication of organic light-emitting diodes with up to 32 % hot exciplex contribution and low efficiency roll-off.


2020 ◽  
Vol 8 (35) ◽  
pp. 12272-12283
Author(s):  
Fulong Ma ◽  
Xinxin Zhao ◽  
Hefang Ji ◽  
Dongdong Zhang ◽  
Kamran Hasrat ◽  
...  

Improving the luminescence efficiency and reverse intersystem crossing of dendritic luminogens with AIE and TADF features by employing a highly twisted molecular configuration and multiple transition channels for solution-processed OLEDs.


2019 ◽  
Vol 3 (6) ◽  
pp. 1181-1191 ◽  
Author(s):  
Chongguang Zhao ◽  
Chen Li ◽  
Yilang Li ◽  
Yong Qiu ◽  
Lian Duan

Shallow trap assisted charge transport, fast reverse intersystem crossing of the hosts and efficient host–guest Förster resonant energy transfer in OLEDs can retard the defect formation by inhibiting exciton–polaron annhilation.


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