Interacting Emission Species among Donor and Acceptor Moieties in a Donor-Grafted Polymer Host/TADF-Guest System and Their Effects on Photoluminescence and Electroluminescence

Thermally activated delayed fluorescence (TADF)-based electroluminescence (EL) devices adopting a host/guest strategy in their emitting layer (EML) are capable of realizing high efficiency. However, TADF emitters composed of donor and acceptor moieties as guests dispersed in organic host materials containing a donor and/or an acceptor are subject to donor-acceptor (D-A) interactions. In addition, electron delocalization between neighboring emitter molecules could form different species of aggregates. Here, we investigate the effects of intermolecular interacting emission species on the optoelectronic properties of sky-blue/green/red (sB/G/R) TADF emitters as guests using poly(biphenyl-Si/Ge) grafted with various donor moieties as hosts. We found the presence of guest/guest exciplex (D<sub>g</sub>/A<sub>g</sub>)*, host/guest exciplexes (D<sub>h</sub>/A<sub>g</sub>)*, and aggregates through the exploration of interactions between neighboring TADF guest molecules and between host and TADF-guest molecules. The nonradiative <sup>3</sup>(D<sub>h</sub>/A<sub>g</sub>)* (Δ<i>E</i><sub>ST</sub> ≈ 0.5 eV) could increase the internal conversion rate (k<sub>IC</sub>) and reduce delayed luminescence, and both of them could cause a decrease in PLQY. The luminescence of <sup>3</sup>(D<sub>h</sub>/A<sub>g</sub>)* may have a positive or negative effect on PLQY depending on its triplet energy. As the singlet and triplet energies of (aggregate)* are lower than those of (ICT)*, energy transfer from (ICT)* to (aggregate)* could occur. The low PLQY nature of (aggregate)* means that it is more likely to cause quenching in device emission. The emissions from (D<sub>h</sub>/A<sub>g</sub>)* and (aggregate)* are found to have increased full width at half-maximum and lead to lower emission color purity. Such intermolecular interactions should also occur in host/guest (TADF) systems and nondoped TADF emitter systems and thus are important factors for the molecular design of the TADF emitter and/or its accompanying host for high device efficiency and emission color purity.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2024-10-24
DOI
https://doi.org/10.1021/acsami.4c15933
Citations
5
Primary Topic
Organic Light-Emitting Diodes Research
Type
article
Field-Weighted Citation Impact
1.04

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article

Interacting Emission Species among Donor and Acceptor Moieties in a Donor-Grafted Polymer Host/TADF-Guest System and Their Effects on Photoluminescence and Electroluminescence

Miao‐Ken Hung, Shang-Ting Chung, Show‐An Chen, Yi‐Hen Mao et al.
5 citations
ACS Applied Materials & Interfaces
Organic Light-Emitting Diodes Research
1.04
article

Interacting Emission Species among Donor and Acceptor Moieties in a Donor-Grafted Polymer Host/TADF-Guest System and Their Effects on Photoluminescence and Electroluminescence

Miao‐Ken Hung, Shang-Ting Chung, Show‐An Chen, Yi‐Hen Mao, Kuen‐Wei Tsai, Sunil Kumar Sharma
article en
5 citations

Abstract

Thermally activated delayed fluorescence (TADF)-based electroluminescence (EL) devices adopting a host/guest strategy in their emitting layer (EML) are capable of realizing high efficiency. However, TADF emitters composed of donor and acceptor moieties as guests dispersed in organic host materials containing a donor and/or an acceptor are subject to donor-acceptor (D-A) interactions. In addition, electron delocalization between neighboring emitter molecules could form different species of aggregates. Here, we investigate the effects of intermolecular interacting emission species on the optoelectronic properties of sky-blue/green/red (sB/G/R) TADF emitters as guests using poly(biphenyl-Si/Ge) grafted with various donor moieties as hosts. We found the presence of guest/guest exciplex (D<sub>g</sub>/A<sub>g</sub>)*, host/guest exciplexes (D<sub>h</sub>/A<sub>g</sub>)*, and aggregates through the exploration of interactions between neighboring TADF guest molecules and between host and TADF-guest molecules. The nonradiative <sup>3</sup>(D<sub>h</sub>/A<sub>g</sub>)* (Δ<i>E</i><sub>ST</sub> ≈ 0.5 eV) could increase the internal conversion rate (k<sub>IC</sub>) and reduce delayed luminescence, and both of them could cause a decrease in PLQY. The luminescence of <sup>3</sup>(D<sub>h</sub>/A<sub>g</sub>)* may have a positive or negative effect on PLQY depending on its triplet energy. As the singlet and triplet energies of (aggregate)* are lower than those of (ICT)*, energy transfer from (ICT)* to (aggregate)* could occur. The low PLQY nature of (aggregate)* means that it is more likely to cause quenching in device emission. The emissions from (D<sub>h</sub>/A<sub>g</sub>)* and (aggregate)* are found to have increased full width at half-maximum and lead to lower emission color purity. Such intermolecular interactions should also occur in host/guest (TADF) systems and nondoped TADF emitter systems and thus are important factors for the molecular design of the TADF emitter and/or its accompanying host for high device efficiency and emission color purity.

ACS Applied Materials & InterfacesVol. 16(44)
National Tsing Hua University (TW)
Ministry of Science and Technology, Taiwan
Openalex Percentile: Top 23%
Organic Light-Emitting Diodes Research
1.04
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