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.

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

2,4 Difluoro PTAA Distribution Plot