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Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine)

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Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) Basic information

Product Name:
Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine)
Synonyms:
  • Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine)
  • TFB AldrichCPR
  • s-TFB,Poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-(4,4’-(N-(4-sec-butyl- phenyl)diphenylamine)
  • P-200 Poly(9,9-dioctylfluorene-co-N-(4-(1-methylpropyl) phenyl)diphenylamine)
  • Polyimino]-1,4-phenylene(9,9-dioctyl-9H-fluorene-2,7-diyl)-1,4-phenylene]
  • 4-(sec-Butyl)-N-(4-(9,9-dioctyl-7-phenyl-9H-fluoren-2-yl)phenyl)aniline(poly)
  • Poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-(4,4'-(N-(4-sec-butylphenyl) diphenylamine)]
  • N-(4-(sec-butyl)phenyl)-N-(4-(9,9-dioctyl-7-phenyl-9H-fluoren-2-yl)phenyl)-[1,1'-biphenyl]-4-amine
CAS:
220797-16-0
MF:
C51H63N
MW:
690.05262
Mol File:
220797-16-0.mol
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Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) Chemical Properties

Melting point:
166.2℃
form 
powder
color 
yellow
InChIKey
RBFSUOVKQODUII-UHFFFAOYSA-N
SMILES
N(C1=CC=C(C(CC)C)C=C1)C1=CC=C(C2C=CC3C4=C(C(CCCCCCCC)(CCCCCCCC)C=3C=2)C=C(C2=CC=CC=C2)C=C4)C=C1
Solvent
THF, Toluene and Chloroform
Absorption
λmax?390 nm (in THF)
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Poly(9,9-dioctylfluorene-co-N-(4-butylphenyl)diphenylamine) Usage And Synthesis

Classification

Hole transport material (HTL), Hole injection material (HIL), Electron blocking material (EBL), OLEDs, Perovskite solar cells, Organic and printed electronics.

Applications

Poly(9,9-dioctylfluorene-alt-N-(4-sec-butylphenyl)-diphenylamine) (TFB) is a triarylamine based semiconductor with a band gap of 3 eV (HOMO and LUMO levels of 5.3 and 2.3 eV, respectively) and a relatively high hole mobility of 2 ×10-3 cm2 V-1 s-1.
Due to its low ionisation potential and high hole mobility, TFB serves primarily as hole transport layer (HTL), hole-injection layer (HIL) and electron-blocking layer (EBL) material in organic electronic devices. When built into device as an interface material, TFB as an electron blocking layer will not only reduce the chance of electron leakage, but also reduce the possibility of exciton quenching between the interface of the active layer and charge transport layer (F8BT/MoOx for example).

Description

Poly(9,9-dioctylfluorene-alt-N-(4-sec-butylphenyl)-diphenylamine) (TFB) is a triarylamine based semiconductor with a band gap of 3 eV (HOMO and LUMO levels of 5.3 and 2.3 eV, respectively) and a relatively high hole mobility of 2 ×10-3 cm2 V-1 s-1.

Uses

TFB can be used in the formation of multilayer quantum dot-based light-emitting diodes (LEDs). It can also be used in the fabrication of highly responsive gas sensors for breath analysis.

Uses

TFB can be used for a variety of optoelectronic applications such as organic light emitting diodes (OLEDs), quantum dot displays (QDs) and solar cells.

General Description

TFB, a hole transporting material and an electron-blocking layer, has high hole mobility, low electron affinity, and high ionic potential. Its electron blocking nature results in effective confinement of injected charge carriers in the perovskite layers.

References

[1] Hwang, Jaehyung and A. Kahn. “Interface energetics of polyfluorene and fluorene-arylamine copolymers.” SPIE Optics + Photonics 5 1 (2006): 0.
[2] Yajun Xia, R. Friend. “Polymer bilayer structure via inkjet printing.” Applied Physics Letters 88 1 (2006): 163508.

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