Photocurrent enhancement and photoresponse properties of organic photodetectors with iridium complexes doped in conjugated polymers
Source abstract
Abstract
Abstract Properties of solution-processed organic photodetectors with iridium (Ir) complexes doped in fluorene-type conjugated polymer, poly(dioctylfluorene-co-benzothiadiazole) [F8BT] as a host were investigated. F8BT devices had blue sensitivity. Ir complexes as triplet materials can enhance the incident-photon-to-current conversion efficiency (IPCE) of the devices when their triplet levels are lower than the lowest excited singlet states (S 1 ) of the host and higher than the lowest excited triplet states (T 1 ) of the host. A bilayer F8BT device utilizing solution-processable starburst molecular and tris(2-phenylpyridine)iridium(III) [Ir(ppy) 3 ] as a hole transporting layer and a dopant, respectively, showed larger photocurrent than an non-doped bilayer device under high applied voltage. For the bilayer device with Ir(ppy) 3, a cut-off frequency of more than 10 MHz was observed under forward bias of 5 V and clear response pulses at 10 MHz were received using a sinusoidal modulated laser light illumination.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (20)
Show source-provided references
1. Baldo · Appl. Phys. Lett. · 1999 · 75 · 410.1063/1.124258 ↗
2. Adachi · Appl. Phys. Lett. · 2001 · 78 · 162210.1063/1.1355007 ↗
3. Peumans · Appl. Phys. Lett. · 2000 · 76 · 385510.1063/1.126800 ↗
4. Ohmori · IEEE J. Sel. Top. Quantum Electron. · 2004 · 10 · 7010.1109/JSTQE.2004.824106 ↗
5. Morimune · IEEE J. Disp. Technol. · 2006 · 2 · 17010.1109/JDT.2006.874505 ↗
6. Morimune · IEEE Photonics Technol. Lett. · 2006 · 18 · 266210.1109/LPT.2006.887786 ↗
7. Shao · Adv. Mater. · 2005 · 17 · 284110.1002/adma.200501297 ↗
8. Zhihua · Appl. Phys. Lett. · 2006 · 89 · 13111610.1063/1.2357584 ↗
9. Westenhoff · J. Am. Chem. Soc. · 2008 · 130 · 1365310.1021/ja803054g ↗
10. Ohmori · Jpn. J. Appl. Phys. · 1991 · 30 · L194110.1143/JJAP.30.L1941 ↗
11. Asada · Jpn. J. Appl. Phys. · 2006 · 45 · L24710.1143/JJAP.45.L247 ↗
12. Chua · Nature · 2005 · 434 · 19410.1038/nature03376 ↗
13. Kajii · Jpn. J. Appl. Phys. · 2008 · 47 · 315210.1143/JJAP.47.3152 ↗
14. Kajii · Org. Electron. · 2010 · 11 · 50910.1016/j.orgel.2009.12.004 ↗
15. Cook · Appl. Phys. Lett. · 2006 · 89 · 10112810.1063/1.2338528 ↗
16. Tsuboyama · J. Am. Chem. Soc. · 2003 · 125 · 1297110.1021/ja034732d ↗
17. Matsusue · Jpn. J. Appl. Phys. · 2005 · 44 · 369110.1143/JJAP.44.3691 ↗
18. Elschner · Synth. Met. · 2000 · 111 · 13910.1016/S0379-6779(99)00328-8 ↗
19. Hino · Org. Electron. · 2004 · 5 · 26510.1016/j.orgel.2004.07.001 ↗
20. Kajii · Jpn. J. Appl. Phys. · 2011 · 50 · 04DK0510.1143/JJAP.50.04DK05 ↗