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Published TCIMAIL newest issue No.198
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CAS RN: 110134-47-9 | Product Number: P2513
Poly(3-hexylthiophene-2,5-diyl) (regioregular) [for organic electronics]
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Purity:
Synonyms:
- P3HT (regioregular)
Product Documents:
| Size | Unit Price | Belgium | Japan* | Quantity |
|---|---|---|---|---|
| 100MG |
€197.00
|
1 | 30 |
|
| 500MG |
€630.00
|
1 | 19 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
| Product Number | P2513 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| Condition to Avoid | Light Sensitive |
| Packaging and Container | 100MG-Glass Bottle with Plastic Insert (View image), 500MG-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 110134-47-9 |
| Related CAS RN | 156074-98-5&104934-50-1&125321-66-6 |
| Reaxys Registry Number | 8828732 |
Specifications
| Hole Mobility(mu FET) | min 0.10cm2/Vs (OTS Si/SiO2 substrate) |
| Palladium | max. 100 ppm |
| Molecular weight of number average | 27000 to 45000 |
| Stereoregularity | min. 99.0 % |
Properties (reference)
| HOMO Level | -4.8 eV |
GHS
Related Laws:
Transport Information:
| HS Number | 3911909990 |
Application
High-Regioregular P3HT-Based Transistor Realizing Hole Mobility of Over 20 cm2/Vs
References
- Electric-double-layer field-effect transistors with ionic liquids
- High-Performance Organic Field-Effect Transistors Gated by Imidazolium-Based Ionic Liquids
Application
Highly Regioselective Organic Semiconducting Polymer: P3HT
P3HT was synthesized by a direct arylation polymerization (DArP)1,2) and features a highly regioselective structure with a consistent average molecular weight and polydispersity index. In addition, P3HT is useful for solution process-able organic solar cells,3,4) perovskite solar cells,5) and organic transistor research,6) due in part to its high solubility.
Figure 1. Organic Photovoltaics (OPV)
Figure 2. Perovskite Solar Cell (PSC)
Figure 3. Organic Transistor (OFET)
This material was produced by collaboration with Prof. Fumiyuki Ozawa
at Institute for Chemical Research, Kyoto University.
References
- 1)Palladium-catalyzed dehydrohalogenative polycondensation of 2-bromo-3-hexylthiophene: An efficient approach to head-to-tail poly(3-hexylthiophene)
- 2)Structural analysis of poly(3-hexylthiophene) prepared via direct heteroarylation polymerization
- 3)A review of recent plasmonic nanoparticles incorporated P3HT: PCBM Organic thin film solar cells
- 4)Poly(3-hexylthiophene): Synthetic methodologies and properties in bulk heterojunction solar cells
- 5)Hole-transport materials for perovskite solar cells
- 6)25th Anniversary article: Organic field-effect transistors: The path beyond amorphous silicon
Documents
Product Articles
[TCIMAIL No.176] Highly Regioselective Organic Semiconducting Polymer: P3HT[Product Highlights] High-Regioregular P3HT-Based Transistor Realizing Hole Mobility of Over 20 cm2/Vs
[Product Highlights] High Regioregular p-type Organic Semiconducting Polymer
[Organic Transistor] Performance evaluation of highly regioregular “P3HT”
[Organic Transistor] Fabrication and Evaluation of Organic Field-Effect Transistors (OFETs) : P3HT
Product Documents (Note: Some products will not have analytical charts available.)
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