F8BT (PFBT)
CAS Number 210347-52-7
OFET & OLED Polymer Materials, Perovskite Interface Materials, Perovskite Materials, Semiconducting Polymers
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F8BT (PFBT), popular green emitting polymer
High purity (>99.9%) and available for priority dispatch
A widely used green emitting reference polymer for a variety of applications including as an emissive species in OLEDs [1], an approximately balanced p-type and n-type polymer for OFETs [2] and light emitting transistors [3] as well as being used a polymeric accepter for OPVs [1]. The deep lying HOMO and LUMO levels (5.9 / 3.3 eV) makes it air stable while the liquid-crystalline and beta phases make it widely used for basic research purposes.
General Information
Full name | Poly(9,9-dioctylfluorene-alt-benzothiadiazole) |
Synonyms | F8BT, PFBT |
Chemical formula | (C35H42N2S)n |
CAS number | 210347-52-7 |
HOMO / LUMO | HOMO = -5.9 eV, LUMO = -3.3 eV [2] |
Classification / Family | Polyfluorenes, Benzothiodiazoles, Organic semiconducting materials, Semiconducting polymers, OLED green emitter materials, OLED materials, Organic Photovoltaic materials, Polymer solar cells, OFET materials |
Product Details
Purity | > 99.9% |
Appearance | Orange powder/flakes |
Chemical Structure

Device Structure(s)
Device structure | ITO/PEDOT:PSS/TFB/F8BT/F8imBT-Br*/Ca/Al [4] |
Colour |
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Max. EQE | 5.1% |
Max. Current Efficiency | 17.9 cd/A |
Max. Power Efficiency | 16.6 lm W−1 |
Usage Datasheet
For a high efficiency green OLED we recommend blending F8 (PFO) with F8BT with the below specifications. This ink can then be deposited either in air or in a glove box with little difference in performance, provided that the exposure time and light levels are minimised. For more details see our fabrication guide.
At typical concentrations of 10 mg/ml 100 mg of F8 (PFO) will make around 200 spin-coated devices on Ossila's standard ITO substrates (20 x 15 mm) assuming 50% solution usage (50% loss in filtering and preparation).
OLED reference device:
- F8 with F8BT
- Blend ratio of 19:1 (F8:F8BT) in Toluene
- Total concentration of 10 mg/ml
- 0.45 μm PTFE (hydrophobic) filter
- Spun at 2000 rpm (approx. 70 nm thickness)
Pipetting 20 μl of the above solutions onto a substrate spinning at 2000 rpm should provide a good even coverage with approximately 70 nm thickness. The substrate needs to be spun until dry, which is typically only a few seconds — 15 seconds should be ample to achieve this. Thermal annealing should be undertaken at 80°C for 10 minutes prior to cathode deposition
A basic but efficient OLED can be made using PEDOT:PSS as a hole transport layer and Calcium/Aluminum as the electron contact. When used with the Ossila ITO substrates and shadow masks this produces an easy to fabricate yet efficient >100 cd/m2) device.

Technical Data
Product Code | Soluble solvents | Recommended Processing Solvents at 10mg/ml |
M0231A4 | Chloroform, chlorobenzene | Chlorobenzene |
M0231A5 | Toluene, chloroform, chlorobenzene | Toluene |
M0231A6 | Toluene, chloroform, chlorobenzene | Toluene |
M0231A7 | Toluene, chloroform, chlorobenzene | Toluene |
M0231A8 | Toluene, chloroform, chlorobenzene | Toluene |
Batch details
Batch number | MW | Mn | PDI | Stock info |
M0231A4* | 503,486 | 187,303 | 2.69 | In stock |
M0231A5 | 167,248 | 65,077 | 2.57 | Discontinued |
M0231A6 | 201,357 | 69,906 | 2.88 | Discontinued |
M0231A7 | 62,768 | 29,903 | 2.10 | In stock |
M0231A8 | 298,964 | 78,719 | 3.80 | In stock |
*Recommended processing solvent for M0231A4 is chlorobenzene for its high molecular weights.
Pricing
Batch | 250 mg | 500 mg | 1 g |
---|---|---|---|
M0231A4/A8 | £330 | £560 | £950 |
M0231A7 | £210 | £340 | £600 |
MSDS Documentation
Literature and References
Please note that Ossila has no formal connection to any other authors or institutions in these references.
- Conjugated-Polymer Blends for Optoelectronics. C.R. McNeill et al., Advanced Materials, Vol 21, Issue 38-39, 3840 (2009)
- Electron and hole transport in poly(fluorene-benzothiadiazole). Y. Zhang et al., Appl. phys. Lett., Vol 98, 143504 (2011)
- Organic Light Emitting Field Effect Transistors: Advances and Perspectives. F. Cicoira et al., Advanced Functional Materials, Vol 17, Issue 17, 3421-3434 (2007)
- 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.
To the best of our knowledge the information provided here is accurate. The values provided are typical at the time of manufacture and may vary over time and from batch to batch. Products may have minor cosmetic differences (e.g. to the branding) compared to the photos on our website. All products are for laboratory and research and development use only.