Substituent position engineering of diphenylquinoline-based Ir(iii) complexes for efficient orange and white PhOLEDs with high color stability/low efficiency roll-off using a solution-processed emission layer. Issue 1 (27th November 2015)
- Record Type:
- Journal Article
- Title:
- Substituent position engineering of diphenylquinoline-based Ir(iii) complexes for efficient orange and white PhOLEDs with high color stability/low efficiency roll-off using a solution-processed emission layer. Issue 1 (27th November 2015)
- Main Title:
- Substituent position engineering of diphenylquinoline-based Ir(iii) complexes for efficient orange and white PhOLEDs with high color stability/low efficiency roll-off using a solution-processed emission layer
- Authors:
- Sarada, Ganguri
Yoon, Juho
Cho, Woosum
Cho, Minji
Cho, Daw Won
Kang, Sang Ook
Nam, Yeonsig
Lee, Jin Yong
Jin, Sung-Ho - Abstract:
- Abstract : The location of –CF3 group on 2, 4-diphenylquinoline based Ir(iii ) complexes is key for attaining high performance in solution-processed PhOLEDs. Abstract : Three new heteroleptic Ir(iii ) complexes o -LIrpic, m -LIrpic, and p -LIrpic (L = CF3 DPQ) consisting of 2, 4-diphenylquinoline (DPQ) with a –CF3 group at ortho ( o )/ meta ( m )/ para ( p ) positions of the metalated phenyl ring, respectively, as the main ligands were synthesized and used as emitters in phosphorescent organic light-emitting diodes (PhOLEDs). We realized that –CF3 position extremely affects the crucial photophysical and electronic properties such as emission color, photoluminescence quantum yield (PLQY) and energy levels of these Ir(iii ) complexes resulting in –CF3 position-dependent performance of their PhOLEDs. To verify the effect of –CF3 group position on device performance, three other Ir(iii ) complexes o -LIrtmd, m -LIrtmd, and p -LIrtmd were synthesized using the same main ligands but a different ancillary ligand. In the two series of Ir(iii ) complexes, the devices with m -CF3 based complexes are outstanding in performance compared to o - or p -CF3 based ones due to the enhanced PLQY and well suppressed non-radiative deactivations by m -substitution. Finally, the single emission layer solution-processed orange and two-component white PhOLEDs fabricated using m -LIrpic as orange emitter achieved the maximum external quantum efficiency of 17.1% (43.9 cd A −1 ) and 21.1% (48.8 cd A −1Abstract : The location of –CF3 group on 2, 4-diphenylquinoline based Ir(iii ) complexes is key for attaining high performance in solution-processed PhOLEDs. Abstract : Three new heteroleptic Ir(iii ) complexes o -LIrpic, m -LIrpic, and p -LIrpic (L = CF3 DPQ) consisting of 2, 4-diphenylquinoline (DPQ) with a –CF3 group at ortho ( o )/ meta ( m )/ para ( p ) positions of the metalated phenyl ring, respectively, as the main ligands were synthesized and used as emitters in phosphorescent organic light-emitting diodes (PhOLEDs). We realized that –CF3 position extremely affects the crucial photophysical and electronic properties such as emission color, photoluminescence quantum yield (PLQY) and energy levels of these Ir(iii ) complexes resulting in –CF3 position-dependent performance of their PhOLEDs. To verify the effect of –CF3 group position on device performance, three other Ir(iii ) complexes o -LIrtmd, m -LIrtmd, and p -LIrtmd were synthesized using the same main ligands but a different ancillary ligand. In the two series of Ir(iii ) complexes, the devices with m -CF3 based complexes are outstanding in performance compared to o - or p -CF3 based ones due to the enhanced PLQY and well suppressed non-radiative deactivations by m -substitution. Finally, the single emission layer solution-processed orange and two-component white PhOLEDs fabricated using m -LIrpic as orange emitter achieved the maximum external quantum efficiency of 17.1% (43.9 cd A −1 ) and 21.1% (48.8 cd A −1 ), respectively, with highly stable color coordinates and low efficiency roll-off. This is the highest efficiency reported to date for solution-processed orange PhOLEDs using a small molecular host with easily accessible emitter. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 4:Issue 1(2016)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 4:Issue 1(2016)
- Issue Display:
- Volume 4, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 4
- Issue:
- 1
- Issue Sort Value:
- 2016-0004-0001-0000
- Page Start:
- 113
- Page End:
- 120
- Publication Date:
- 2015-11-27
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5tc03004h ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1657.xml