Electron donor and acceptor for highly efficient photovoltaic and OLED applications
5,10,15,20-Tetraphenylbisbenz[5,6]indeno[1,2,3-cd:1′,2′,3′-lm]perylene (DBP), also known as tetraphenyldibenzoperiflanthene, is a promising organic small-molecule semiconductor. It can be used as either an electron donor or acceptor for highly efficient photovoltaic and OLED applications.
With perylene as an electron-rich core and extended conjugations, DBP can also be used in photovoltaic light-emitting diodes (PVOLEDs) devices as an electron-donating layer (EDL) material.
*For chemical structure information, please refer to the cited references.
Pricing
Grade
Order Code
Quantity
Price
Sublimed (>99.0% purity)
M2101A1
250 mg
[[price gbp="400"]]
Sublimed (>99.0% purity)
M2101A1
500 mg
[[price gbp="680"]]
Sublimed (>99.0% purity)
M2101A1
1 g
[[price gbp="1150"]]
MSDS Documentation
Literature and Reviews
High-Efficiency White Organic Light-Emitting Diodes Based on a Blue Thermally Activated Delayed Fluorescent Emitter Combined with Green and Red Fluorescent Emitters, T. Higuchi et al., Adv. Mater., 27, 2019–2023 (2015); DOI: 10.1002/adma.201404967.
High efficiency red organic light-emitting devices using tetraphenyldibenzoperiflanthene-doped rubrene as an emitting layer, K. Okumoto et al., Appl. Phys. Lett. 89, 013502 (2006); doi: 10.1063/1.2218833.
High-Efficiency WOLEDs with High Color-Rendering Index based on a Chromaticity-Adjustable Yellow Thermally Activated Delayed Fluorescence Emitter, X. Li et al., Adv. Mater., 28, 4614–4619 (2016); DOI: 10.1002/adma.201505963.
Efficient solution-processed red all-fluorescent organic light-emitting diodes employing thermally activated delayed fluorescence materials as assistant hosts: molecular design strategy and exciton dynamic analysis, D. Chen et al., J. Mater. Chem. C, 5, 5223-5231 (2017); DOI: 10.1039/C7TC01164D.
Organic Solar Cells with Open Circuit Voltage over 1.25 V Employing Tetraphenyldibenzoperiflanthene as the Acceptor, A. Bartynski et al., J. Phys. Chem. C, 120 (34), 19027–19034 (2016); DOI: 10.1021/acs.jpcc.6b06302.