A bipolar triphenylamine-dibenzothiophene S, S-dioxide hybrid compound for solution-processable single-layer green OLEDs and as a host for red emitters. (10th April 2019)
- Record Type:
- Journal Article
- Title:
- A bipolar triphenylamine-dibenzothiophene S, S-dioxide hybrid compound for solution-processable single-layer green OLEDs and as a host for red emitters. (10th April 2019)
- Main Title:
- A bipolar triphenylamine-dibenzothiophene S, S-dioxide hybrid compound for solution-processable single-layer green OLEDs and as a host for red emitters
- Authors:
- Jiang, Qinglin
Xu, Yuwei
Yu, Tiancheng
Qiu, Xu
Zhao, Ruiyang
Zhao, Duokai
Zheng, Nan
Hu, Dehua
Xie, Zengqi
Ma, Yuguang - Abstract:
- Abstract : A bipolar triphenylamine-dibenzothiophene S, S -dioxide hybrid compound for solution-processable single-layer green OLEDs and as a host for red emitters. Abstract : A novel bipolar compound triphenylamine-dibenzothiophene S, S -dioxide (TPAFSO) based on a dibenzothiophene- S, S -dioxide (DBTO) moiety and a triphenylamine (TPA) unit, in which the TPA unit is linked at its 4-position to the DBTO group at its 3, 7-position, is designed and synthesized. The experimental results clearly show that TPAFSO exhibits a high photoluminescence efficiency of 0.52 in a film form and good/balanced carrier injecting properties, as well as an adequate triplet energy ( E T ) of 2.1 eV to sensitize red phosphor. Hence, solution-processable single-layer green OLEDs using TPAFSO as emitters exhibit a maximum luminous efficiency (LE) of 4.7 cd A −1 and a maximum brightness of 5952 cd m −2 with a low turn-on voltage of 2.5 V, which is superior to the performance of double-layer devices. Furthermore, considering the TPAFSO as a solution-processed host for red emitters, 5% bis(2-(2′-benzothienyl)-pyridinato- N, C 3 ′)iridium(acetylacetonate) (Ir(btp)2 (acac))-doped single-layer devices give a maximum quantum yield of 3.9% and a saturated red emission with CIE coordinates of (0.68, 0.32), which are much better than that of Ir(btp)2 (acac)-doped poly( N -vinylcarbazole)-2- tert -butylphenyl-5-biphenyl-1, 3, 4-oxadiazole (PVK-PBD) single-layer devices. Additionally, the red OLEDs usingAbstract : A bipolar triphenylamine-dibenzothiophene S, S -dioxide hybrid compound for solution-processable single-layer green OLEDs and as a host for red emitters. Abstract : A novel bipolar compound triphenylamine-dibenzothiophene S, S -dioxide (TPAFSO) based on a dibenzothiophene- S, S -dioxide (DBTO) moiety and a triphenylamine (TPA) unit, in which the TPA unit is linked at its 4-position to the DBTO group at its 3, 7-position, is designed and synthesized. The experimental results clearly show that TPAFSO exhibits a high photoluminescence efficiency of 0.52 in a film form and good/balanced carrier injecting properties, as well as an adequate triplet energy ( E T ) of 2.1 eV to sensitize red phosphor. Hence, solution-processable single-layer green OLEDs using TPAFSO as emitters exhibit a maximum luminous efficiency (LE) of 4.7 cd A −1 and a maximum brightness of 5952 cd m −2 with a low turn-on voltage of 2.5 V, which is superior to the performance of double-layer devices. Furthermore, considering the TPAFSO as a solution-processed host for red emitters, 5% bis(2-(2′-benzothienyl)-pyridinato- N, C 3 ′)iridium(acetylacetonate) (Ir(btp)2 (acac))-doped single-layer devices give a maximum quantum yield of 3.9% and a saturated red emission with CIE coordinates of (0.68, 0.32), which are much better than that of Ir(btp)2 (acac)-doped poly( N -vinylcarbazole)-2- tert -butylphenyl-5-biphenyl-1, 3, 4-oxadiazole (PVK-PBD) single-layer devices. Additionally, the red OLEDs using 4-(dicyanomethylene)-2- t -butyl-6-(1, 1, 7, 7-tetramethyljulolidyl-9-enyl)-4 H pyran (DCJTB)-doped TPAFSO as the emitting layer exhibit a maximum LE of 1.8 cd A −1, and can be compared to the performances of DCJTB/Alq3 -based multilayer devices via an evaporation process. … (more)
- Is Part Of:
- New journal of chemistry. Volume 43:Number 17(2019)
- Journal:
- New journal of chemistry
- Issue:
- Volume 43:Number 17(2019)
- Issue Display:
- Volume 43, Issue 17 (2019)
- Year:
- 2019
- Volume:
- 43
- Issue:
- 17
- Issue Sort Value:
- 2019-0043-0017-0000
- Page Start:
- 6721
- Page End:
- 6727
- Publication Date:
- 2019-04-10
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c9nj00537d ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10249.xml