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Luminosyn? F8T2 is now available featuring:
- High purity - higher purity means more precise emission and longer life-time for OLED devices - F8T2 is purified via Soxhlet extraction with methanol, hexane and chloroform under an argon atmosphere
- Good solubility in most of common solvents (toluene, chloroform and chlorobenzene)
- Larger quantity orders so you can plan your experiments with polymer from the same batch)
Pricing
Batch | Quantity | Price |
M502 | 250 mg | £199.8 |
M502 | 1 g | £679.3 |
M502 | 5 g / 10 g* | Please enquire |
*For 5 - 10 grams order quantity, the lead time is 4-6 weeks.
Batch information
Batch | Mw | Mn | PDI | |
M501 | >50,000 | <3.0 |
|
|
M502 | 136,320 | 53,866 | 2.53 |
|
General Information
CAS number | 210347-56-1 |
Chemical formula | (C37H44S2)n |
Molecular weight | See batch information for details |
HOMO / LUMO | HOMO = 5.5 eV / LUMO = 3.1 eV [1] |
Synonyms | PFOT, Poly(9,9-dioctylfluorene-alt-bithiophene), Poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-bithiophene] |
Classification / Family | Polyfluorenes, Bithiophenes, Heterocyclic five-membered ring, Organic semiconducting materials, PLED green emitter materials, Organic Photovoltaics, Polymer Solar Cells, Light-emitting Diodes, OFET materials |
Suggested Solvents | Chloroform, chlorobenzene or dichlorobenzene |
Applications
Poly(9,9-
The absorption in the blue region of F8T2 makes it an excellent donor polymer to blend with an acceptor having complementary spectrum or assemble a tandem cell with other low bandgap-conjugated polymers with absorption extended in the red region.
Device structure |
ITO/PEDOT:PSS/TFB/F8T2/Ca [3] |
Colour | Green |
Max. Luminance | 23,400 |
Max. Current Efficiency | 3.68 cd/A |
Max. Power Efficiency | 2.9?lm?W?1 |
Literature and Reviews
- Annealing effect of polymer bulk heterojunction solar cells based on polyfluorene and fullerene blend, J-H. Huang et al., Org. Electronics, 10, 27–33 (2009), doi:10.1016/j.orgel.2008.09.007.
- High-Efficiency Polymer LEDs with Fast Response Times Fabricated via Selection of Electron-Injecting Conjugated Polyelectrolyte Backbone Structure, M. Suh et al., ACS Appl. Mater. Interfaces, (2015), DOI: 10.1021/acsami.5b07862.
- On the use and influence of electron-blocking interlayers in polymer light-emitting diodes, R. Jin et al., Phys. Chem. Chem. Phys., 11, 3455-3462 (2009). DOI: 10.1039/B819200F.
- High-Resolution Inkjet Printing of All-Polymer Transistor Circuits, H. Sirringhaus et al., Science, 290 (5499), 2123-2126 (2000), DOI: 10.1126/science.290.5499.2123.
- Organic Light-Emitting Diodes Based on Poly(9,9-dioctylfluorene-co-bithiophene) (F8T2), P. Levermore et al., Adv. Funct. Mater., 19, 950–957 (2009); DOI: 10.1002/adfm.200801260.
- Mobility enhancement in conjugated polymer field-effect transistors through chain alignment in a liquid-crystalline phase, H. Sirringhaus et al., Appl. Phys. Lett. 77, 406 (2000); http://dx.doi.org/10.1063/1.126991.
- Annealing effect of polymer bulk heterojunction solar cells based on polyfluorene and fullerene blend, J-H. Huang et al., Org. Electronics, 10, 27–33 (2009), doi:10.1016/j.orgel.2008.09.007.
- Hole mobility effect in the efficiency of bilayer heterojunction polymer/C60 photovoltaic cells, A. Macedo et al., Appl. Phys. Lett. 98, 253501 (2011); http://dx.doi.org/10.1063/1.3601476.