Aryl-Substituted Acridine Donor Derivatives Modulate the Transition Dipole Moment Orientation and Exciton Harvesting Properties of Donor–Acceptor TADF Emitters

Thermally activated delayed fluorescence (TADF) compounds are highly attractive as sensitizing and emitting materials for organic light-emitting diodes (OLEDs). The efficiency of the OLED depends on multiple parameters, most of which rely on the properties of the emitter including those that govern the internal quantum and outcoupling efficiencies. Herein, we investigate a series of aryl substituted acridine donor derivatives of the donor-acceptor TADF emitter <b>DMAC-TRZ</b>, with the objective of correlating their properties, such as triplet harvesting efficiency and transition dipole moment orientation, with their corresponding device efficiency. The decoration of the DMAC donor with substituted aryl groups not only modifies the molecular weight and length of the emitter but also affects the emission color and the capacity for the emitters to efficiently harvest triplet excitons. The presence of electron-withdrawing 4-cyanophenyl and 4-trifluoromethylphenyl groups in, respectively, <b>CNPh-DMAC-TRZ</b> and <b>CF3Ph-DMAC-TRZ</b>, blue-shifts the emission spectrum but slows down the reverse intersystem crossing rate constant (<i>k</i> <sub>RISC</sub>), while the opposite occurs in the presence of electron-donating groups in <b><sup><i>t</i></sup> BuPh-DMAC-TRZ</b> and <b>OMePh-DMAC-TRZ</b> (red-shifted emission spectrum and faster <i>k</i> <sub>RISC</sub>). In contrast to our expectations, the OLED performance of the five DMAC-TRZ derivatives does not scale with their degree of horizontal emitter orientation but follows the <i>k</i> <sub>RISC</sub> rates. This, in turn, demonstrates that triplet harvesting (and not horizontal emitter orientation) is the dominant effect for device efficiency using this family of emitters. Nonetheless, highly efficient OLEDs were fabricated with <b><sup><i>t</i></sup> BuPh-DMAC-TRZ</b> and <b>OMePh-DMAC-TRZ</b> as emitters, with improved EQE<sub>max</sub> (∼28%) compared to the reference <b>DMAC-TRZ</b> devices.

Authors

Institutions

Publication Details

Journal
The Journal of Physical Chemistry C
Published
2024-08-20
DOI
https://doi.org/10.1021/acs.jpcc.4c03344
Citations
5
Primary Topic
Organic Light-Emitting Diodes Research
Type
article
Field-Weighted Citation Impact
1.04

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Aryl-Substituted Acridine Donor Derivatives Modulate the Transition Dipole Moment Orientation and Exciton Harvesting Properties of Donor–Acceptor TADF Emitters

Prakhar Sahay, Andrew P. Monkman, Ettore Crovini, Wolfgang Brütting et al.
5 citations
The Journal of Physical Chemistry C
Organic Light-Emitting Diodes Research
1.04
article

Aryl-Substituted Acridine Donor Derivatives Modulate the Transition Dipole Moment Orientation and Exciton Harvesting Properties of Donor–Acceptor TADF Emitters

Prakhar Sahay, Andrew P. Monkman, Ettore Crovini, Wolfgang Brütting, Eli Zysman‐Colman, Stuart L. Warriner, Thomas Comerford, Kleitos Stavrou, Bình Minh Nguyên
article en
5 citations

Abstract

Thermally activated delayed fluorescence (TADF) compounds are highly attractive as sensitizing and emitting materials for organic light-emitting diodes (OLEDs). The efficiency of the OLED depends on multiple parameters, most of which rely on the properties of the emitter including those that govern the internal quantum and outcoupling efficiencies. Herein, we investigate a series of aryl substituted acridine donor derivatives of the donor-acceptor TADF emitter <b>DMAC-TRZ</b>, with the objective of correlating their properties, such as triplet harvesting efficiency and transition dipole moment orientation, with their corresponding device efficiency. The decoration of the DMAC donor with substituted aryl groups not only modifies the molecular weight and length of the emitter but also affects the emission color and the capacity for the emitters to efficiently harvest triplet excitons. The presence of electron-withdrawing 4-cyanophenyl and 4-trifluoromethylphenyl groups in, respectively, <b>CNPh-DMAC-TRZ</b> and <b>CF3Ph-DMAC-TRZ</b>, blue-shifts the emission spectrum but slows down the reverse intersystem crossing rate constant (<i>k</i> <sub>RISC</sub>), while the opposite occurs in the presence of electron-donating groups in <b><sup><i>t</i></sup> BuPh-DMAC-TRZ</b> and <b>OMePh-DMAC-TRZ</b> (red-shifted emission spectrum and faster <i>k</i> <sub>RISC</sub>). In contrast to our expectations, the OLED performance of the five DMAC-TRZ derivatives does not scale with their degree of horizontal emitter orientation but follows the <i>k</i> <sub>RISC</sub> rates. This, in turn, demonstrates that triplet harvesting (and not horizontal emitter orientation) is the dominant effect for device efficiency using this family of emitters. Nonetheless, highly efficient OLEDs were fabricated with <b><sup><i>t</i></sup> BuPh-DMAC-TRZ</b> and <b>OMePh-DMAC-TRZ</b> as emitters, with improved EQE<sub>max</sub> (∼28%) compared to the reference <b>DMAC-TRZ</b> devices.

The Journal of Physical Chemistry CVol. 128(34)
University of Leeds (GB), University of St Andrews (GB), University of Augsburg (DE), Durham University (GB)
European Commission, Deutsche Forschungsgemeinschaft, Horizon 2020 Framework Programme, Engineering and Physical Sciences Research Council
Affordable and clean energy
Openalex Percentile: Top 23%
Organic Light-Emitting Diodes Research
1.04
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.