Different RISC rates in benzoylpyridine-based TADF compounds and their implications for solution-processed OLEDs. (November 2020)
- Record Type:
- Journal Article
- Title:
- Different RISC rates in benzoylpyridine-based TADF compounds and their implications for solution-processed OLEDs. (November 2020)
- Main Title:
- Different RISC rates in benzoylpyridine-based TADF compounds and their implications for solution-processed OLEDs
- Authors:
- Berenis, Domantas
Kreiza, Gediminas
Juršėnas, Saulius
Kamarauskas, Egidijus
Ruibys, Virginijus
Bobrovas, Olegas
Adomėnas, Povilas
Kazlauskas, Karolis - Abstract:
- Abstract: Reverse intersystem crossing (RISC) rate is among the key parameters of TADF compounds affecting triplet upconversion and annihilation processes, and thus determining efficiency roll-off in TADF-OLEDs. Herein, control of RISC rate ( k RISC ) in a series of benzoylpyridine-based TADF compounds via carbazole donor linking positions is demonstrated. Regardless of the similar singlet-triplet energy splitting found in the compounds with meta- or para- carbazole linking topologies, meta- Cz compounds exhibited stronger singlet-triplet state coupling resulting in 10-fold larger k RISC (up to ~2 × 10 6 s −1 ) as that in para- Cz counterparts. Different k RISC was shown to have important implications for the solution-processed TADF-OLEDs based on the benzoylpyridines. Explicitly, in the non-doped devices based on neat meta- Cz emissive layers, larger k RISC was crucial for the reduced roll-off. Conversely, in 1.2 wt% rubrene-doped hyperfluorescent devices employing benzoylpyridines as TADF hosts, insignificant roll-off was observed irrespective of k RISC, provided it is above 10 5 s −1 . The obtained results give insight into the possibilities of controlling k RISC in benzoylpyridines and demonstrate its importance for efficiency roll-off of TADF and hyperfluorescent OLEDs. Highlights: New carbazole-benzoylpyridine TADF compounds were synthesized. TADF properties were controlled by donor linking topology. RISC rate affected non-doped OLED performance. No impact of RISC rateAbstract: Reverse intersystem crossing (RISC) rate is among the key parameters of TADF compounds affecting triplet upconversion and annihilation processes, and thus determining efficiency roll-off in TADF-OLEDs. Herein, control of RISC rate ( k RISC ) in a series of benzoylpyridine-based TADF compounds via carbazole donor linking positions is demonstrated. Regardless of the similar singlet-triplet energy splitting found in the compounds with meta- or para- carbazole linking topologies, meta- Cz compounds exhibited stronger singlet-triplet state coupling resulting in 10-fold larger k RISC (up to ~2 × 10 6 s −1 ) as that in para- Cz counterparts. Different k RISC was shown to have important implications for the solution-processed TADF-OLEDs based on the benzoylpyridines. Explicitly, in the non-doped devices based on neat meta- Cz emissive layers, larger k RISC was crucial for the reduced roll-off. Conversely, in 1.2 wt% rubrene-doped hyperfluorescent devices employing benzoylpyridines as TADF hosts, insignificant roll-off was observed irrespective of k RISC, provided it is above 10 5 s −1 . The obtained results give insight into the possibilities of controlling k RISC in benzoylpyridines and demonstrate its importance for efficiency roll-off of TADF and hyperfluorescent OLEDs. Highlights: New carbazole-benzoylpyridine TADF compounds were synthesized. TADF properties were controlled by donor linking topology. RISC rate affected non-doped OLED performance. No impact of RISC rate was observed for rubrene-doped devices. … (more)
- Is Part Of:
- Dyes and pigments. Volume 182(2020)
- Journal:
- Dyes and pigments
- Issue:
- Volume 182(2020)
- Issue Display:
- Volume 182, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 182
- Issue:
- 2020
- Issue Sort Value:
- 2020-0182-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-11
- Subjects:
- Dyes and dyeing -- Periodicals
Pigments -- Periodicals
667.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01437208 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.dyepig.2020.108579 ↗
- Languages:
- English
- ISSNs:
- 0143-7208
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3635.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13908.xml