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Product Code M171-200mg
Price $390

HTL Material to Improve Charge Extraction in OLED/OFET Devices

High quality polymer available with free shipping on qualifying orders


Specifications | MSDS | Literature and Reviews


Methyl or fluoro substituted poly(triarylamines) (PTAAs) are electron rich with diphenylamine as the the backbone and substituted phenyl as side chains. Substituted PTAAs are originally used as hole transport layer (HTL) materials in OLED/OFET devices to improve charge extractions. PTAA can also act as electron blocking layer to reduce the chances of electron–hole recombination and energy loss in electronic devices. Fluorinated PTAA, 1F-PTAA and 2F-PTAA, can effectively downshift the HOMO levels of PTAA derivatives due to the electron deficiency of fluorine, resulting in an increase of VOC hence the power conversion efficiency (PCE) of the device.

Enhance power conversion efficiency PTAA

Enhanced PCE

For high efficiency devices

Reduced electron-hole recombination

Reduced Energy Loss

Reduces electron–hole recombination

High Quality PTAA for OFET Applications

High Quality

High quality and electron rich

Hole-transport layer OFET Applications

Hole Transport Layer

Improved charge extraction

PTAA from Ossila used in high impact paper

PTAA from Ossila was used in the high-impact paper (IF 30.85), Multiply Charged Conjugated Polyelectrolytes as a Multifunctional Interlayer for Efficient and Scalable Perovskite Solar Cells, E. Jung et al., Adv. Mater., 2002333 (2020); DOI: 10.1002/adma.202002333.

A range of substituted poly(triarylamine)'s (PTAA's) for use with small molecules for solution-processed high-mobility films. While PTAA has a relatively modest mobility on its own, it has been gaining interest when used in conjunction with small molecules to provide the combination of good coating parameters and high mobility [1,2].

Note: We also have a PTAA family member (PTAA for perovskites) for perovskite solar cell applications.

Specifications


Name Batch number Mw Mn PDI
4-Fluoro PTAA PE10-338-12 6,000 g/mol 4,020 g/mol 1.5
Dimethyl PTAA PE3-298-27B 6,312 g/mol 4,390 g/mol 1.4
2,4 Difluoro PTAA PE-338-8 4,712 g/mol 3,504 g/mol 1.34

2,4 Difluoro PTAA Distribution Plot


2-4 Difluoro PTAA distribution plot

MSDS Documentation


2,4 Dimethyl PTAA MSDS2,4 Dimethyl PTAA MSDS sheet

4-Fluoro PTAA MSDS4-Fluoro PTAA MSDS sheet

2,4 Difluoro PTAA MSDS2,4 Difluoro PTAA MSDS sheet

Literature and References


  1. Solvent and polymer matrix effects on TIPS-pentacene/polymer blend organic field-effect transistors Do Kyung Hwang et al., Journal of Materials Chemistry, V22, P5531-5537 (2012).
  2. Solution-Processed Small Molecule-Polymer Blend Organic Thin-Film Transistors with Hole Mobility Greater than 5 cm 2 /Vs J. Smith et al., Advanced Materials, V24, P2441-2446 (2012).

Technical Support


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