PPF

PPF, dibenzo[b,d]furan-2,8-diylbis(diphenylphosphine Oxide), contains an electron donating dibenzo[b,d]furan core and two electron deficient diphenylphosphine oxide units. Due to its electron deficient nature, PPF and PPT can be used as electron transport layer materials, and in some cases, to form exciplex as emitting layer materials in TADF-OLED devices.

PPF shows a high triplet energy (E_T = 3.1 eV) and it also can be used as host material for effective triplet excitons confinement in the emissive layer. PPF could also be used as exciton blocking layer material.

General Information

Product Details

*Sublimation is a technique used to obtain ultra pure-grade chemicals. For more details about sublimation, please refer to the Sublimed Materials for OLED devices page.

Chemical Structure

Device Structure(s)

Device structure	ITO (50 nm)/HAT-CN (10 nm)/TAPC (50 nm)/CCP (10 nm)/PPF:TMCz-BO (20 nm)/PPF (10 nm)/B3PyPB (30 nm)/Liq (1 nm)/Al (100 nm) [1]
Colour	Blue
Max. EQE	20.7%

Device structure	ITO (50 nm)/TAPC (70 nm)/CDBP (10 nm)/6 wt% CCX-II:PPF (20 nm)/PPF (10 nm)/BmPyPhB (30 nm)/Liq (1 nm)/Al (80 nm) [2]
Colour	Blue
Max. EQE	25.9%
Max. Current Efficiency	41.1 cd/A
Max. Power Efficiency	35.9 lm/W

Device structure	ITO (50 nm)/HAT-CN (10 nm)/α-NPD (50 nm)/CCP (5 nm)/ 6 wt % DPAc-INN-1:PPF (20 nm)/PPF (10 nm)/TPBi (50 nm)/Liq (1 nm)/Al (100 nm) [3]
Colour	Blue
Max. EQE	12.8%
Max. Current Efficiency	24.2 cd/A
Max. Power Efficiency	18.1 lm/W

Device structure	ITO/HAT-CN (10 nm)/a-NPD (40 nm)/CCP (5 nm)/18 wt% MFAc-PPM:PPF (20 nm)/PPF (10 nm)/TPBi (30 nm)/Liq (1 nm)/Al (100 nm) [4]
Colour	Blue
Max. EQE	20.4%
Max. Current Efficiency	41.7 cd/A
Max. Power Efficiency	37.2 lm/W

*For chemical structure information, please refer to the cited references.

Pricing

MSDS Documentation

PPF MSDS sheet

Literature and Reviews

1. Nanosecond-time-scale delayed fluorescence molecule for deep-blue OLEDs with small efficiency rolloff, J. Kim et al., Nature Commun., 11, 1765 (2020); DOI: 10.1038/s41467-020-15558-5.
2. Blue organic light-emitting diodes realizing external quantum efficiency over 25% using thermally activated delayed fluorescence emitters, T. Miwa et al., SCi. Report, 7, 284 (2017); DOI:10.1038/s41598-017-00368-5.
3. An Isonicotinonitrile-based Blue Thermally Activated Delayed Fluorescence Emitter, I. Park et al., Chem. Lett., 49, 210–213 (2020); DOI:10.1246/cl.190808.
4. Pyrimidine-based twisted donor–acceptor delayed fluorescence molecules: a new universal platform for highly efficient blue electroluminescence, I. Park et al., Chem. Sci., 8, 953 (2017); DOI: 10.1039/c6sc03793c.
5. Bluish green emission from pyrene-pyrazoline containing heterocyclic materials and their electronic properties, A. Karuppusamy et al., J. Luminescence, 194, 718-728 (2017); DOI: 10.1016/j.jlumin.2017.09.042.

To the best of our knowledge the information provided here is accurate. However, Ossila assume no liability for the accuracy of this page. The values provided are typical at the time of manufacture and may vary over time and from batch to batch. All products are for laboratory and research and development use only, and may not be used for any other purpose including health care, pharmaceuticals, cosmetics, food or commercial applications.