Photoactivation of an ionic p-type dopant used in a triarylamine based hole transporting material for enhancing conductivity of solution processed films
•Charge transfer from a triarylamine to the iodonium salt is confirmed.•Quantitative determination of the created free charge carrier concentration.•A photoactivation treatment is introduced, increasing doping efficiency 1000-fold.•The photoactivation is addressed on a molecular level. The ionic com...
Gespeichert in:
Veröffentlicht in: | Synthetic metals 2017-08, Vol.230, p.105-112 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | •Charge transfer from a triarylamine to the iodonium salt is confirmed.•Quantitative determination of the created free charge carrier concentration.•A photoactivation treatment is introduced, increasing doping efficiency 1000-fold.•The photoactivation is addressed on a molecular level.
The ionic compound 4-isopropyl-4′-methyldiphenyliodonium tetrakis-(penta- fluorophenyl-borate) (DPI-TPFB) has been investigated as p-type dopant in a triarylamine (TAA) based hole transporting material (HTM). Charge transfer from the HTM to the iodonium salt has been verified and translates to an increase in conductivity of up to 5 orders of magnitude compared to non-doped HTM. UV photoactivation treatment of HTM:DPI-TPFB in solution was shown to increase conductivity by additional 2–3 orders of magnitude up to 2.6·10−2S/m. The concentration of free charge carriers and the related doping efficiency of DPI-TPFB was derived from current–voltage (I–V) measurements of hole only devices. It was possible to demonstrate that the activation treatment triggers a reaction on the molecular level of the iodonium salt. Possible causes for the increased doping efficiency of the system were explored using density functional theory calculations. |
---|---|
ISSN: | 0379-6779 1879-3290 |
DOI: | 10.1016/j.synthmet.2017.05.012 |