Ir(ppy)3


Order Code: M481
Not in stock

Pricing

 Grade Order Code Quantity Price
Sublimed (>99.5% purity) M481 100 mg £158.00
Unsublimed (>98.0% purity) M482 250 mg £166.00
Sublimed (>99.5% purity) M481 250 mg £298.00
Unsublimed (>98.0% purity) M482 500 mg £263.00
Sublimed (>99.5% purity) M481 500 mg £487.00

General Information

CAS number 94928-86-6
Chemical formula C33H24IrN3
Molecular weight 654.78 g/mol
Absorption λmax 282, 377 nm in THF
Fluorescence λem 513 nm in THF
HOMO/LUMO HOMO 5.6 eV, LUMO 3.0 eV
Synonyms
  • Tris[2-phenylpyridine]iridium(III)
  • Tris(2-phenylpyridinato)iridium(III)
  • Tris[2-phenylpyridine-c2,n]iridium(III)
  • Tris(2-phenylpyridine)iridium(III)
Classification / Family Organometallic complex, Green emitter, Phosphorescence dopant OLEDs, Sublimed materials

 

Product Details

Purity

>99.5% (sublimed)

>98.0% (unsublimed)

Melting point 451 °C
Colour Yellow powder

*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

 Irppy3 chemical structure
 
Chemical Structure of tris(2-phenylpyridine)iridium [Ir(ppy)3]; CAS No. 94928-86-6; Chemical Formula C33H24IrN3

 

Applications

Tris(2-phenylpyridine)iridium(III), Ir(ppy)3, is used widely in organic light-emitting diodes (OLEDs) due to its high quantum yields and thermal stability.

Utilising all of its singlet and triplet excitons for the emission, this green light emitting Ir(ppy)3 exhibits a very bright phosphorescence with an internal quantum yield of almost 100% [1, 2, 3]. It is one of the most successful green-triplet emitters in the rapidly developing field of OLED display technology.

 

Device structure                                            ITO/α-NPD* (50 nm)/7%-Ir(ppy)3:CBP (20 nm)/BCP (10 nm)/tris(8-hydroxyquinoline)aluminum (Alq3) (40 nm)/Mg–Ag (100 nm)/Ag (20 nm)  [4]
Colour Green  green
Max EQE (12.0±0.6)%
Max. Powder Efficiency (45±2) lm W1

 

Device structure                                            ITO/α-NPD* (40 nm)/6%-Ir(ppy)3:CBP (20 nm)/BCP (10 nm)/tris(8-hydroxyquinoline)aluminum (Alq3) (20 nm)/Mg–Ag (100 nm)/Ag (20 nm)  [5]
Colour Green  green
Max EQE 8%
Max. Current Efficiency 28 cd/A
Max. Powder Efficiency 31 lm W1

 

Device structure ITO/PEDOT:PSS (50 nm)/poly-TCZ (35 nm)/1*:Ir(ppy)3 (94:6 wt%)(20 nm)/TAZ (50 nm)/LiF (2.5 nm)/Al (40 nm)/Ag (100 nm) [6]
Colour Blue  blue
Max. Luminance 47,000 cd/m2
Max. Current Efficiency 81.1 cd/A
Max. EQE 25.2%
Max. Power Efficiency 46.8 lm W−1 

 

Device structure ITO/MoO3 (3 nm)/CBP: 20 wt% Ir(ppy)3: 4 wt% FIrpic (30 nm)/TAZ (50 nm) [7]
Colour Green  green
Max. Luminance 27,524 cd/m2
Max. Current Efficiency 71.2 cd/A

 

Device structure 

ITO/NPD/5%BCzVBi:CBP/CBP/4%PQIr*:CBP/5%Ir(ppy)3:CBP/CBP/5%BCzVBi:CBP/

LiF/Al [8]

Colour  White  white
Max EQE 11.0 ± 0.3%
Max. Power Efficiency 22.1 ± 0.3lm W1

 

Device structure                                            ITO/0.4 wt% F4TCNQ doped α NPD (30 nm)/ 5 wt% Ir (ppy)3 doped CBP (50 nm)/BPhen (30 nm)/20 wt% TCNQ mixed BPhen (1.5 nm)/Al [9]
Colour Green  green
Luminance@15 V 1,320 cd/m2 
Power Efficiency@14 V 56.6 lm W1  
Current Efficiency@14 V 23.17 cd/A

*For chemical structure information please refer to the cited references

Characterisations

HPLC-ir(ppy)3

HPLC trace of tris(2-phenylpyridine)iridium [Ir(ppy)3]

Literature and Reviews

  1. Absorption and emission spectroscopic characterization of Ir(ppy)3, W. Holzer et al., Chem. Phys., 308(1-2), 93-102 (2005), doi:10.1016/j.chemphys.2004.07.051.
  2. The Triplet State of fac-Ir(ppy)3, T. Hofbeck et al., Inorg. Chem., 49 (20), 9290–9299 (2010), DOI: 10.1021/ic100872w.
  3. High-efficiency fluorescent organic light-emitting devices using a phosphorescent sensitizer, M. A. Baldo et al., Nature 403, 750-753 (2000) | doi:10.1038/35001541.
  4. Efficient electrophosphorescence using a doped ambipolar conductive molecular organic thin film, C. Adachi et aL., Org. Electronics, 2(1), 37-43 (2001), doi:10.1016/S1566-1199(01)00010-6.
  5. Very high-efficiency green organic light-emitting devices based on electrophosphorescence, M. A. Baldo et al., Appl. Phys. Lett. 75, 4 (1999); http://dx.doi.org/10.1063/1.124258.
  6. Efficient blue-emitting electrophosphorescent organic light-emitting diodes using 2-(3,5-di(carbazol-9-yl)-phenyl)-5-phenyl-1,3,4-oxadiazole as an ambipolar host, Y. Zhang et al., RSC Adv., 3, 23514 (2013). DOI: 10.1039/c3ra43720e.
  7. Simplified phosphorescent organic light-emitting devices using heavy doping with an Ir complex as an emitter, Y. Miao et al., RSC Adv., 5, 4261 (2015). DOI: 10.1039/c4ra13308k.
  8. Management of singlet and triplet excitons for efficient white organic light-emitting devices, Y. Sun, et al, Nature 440, 908-912 (2006), doi:10.1038/nature04645.
  9. Novel organic electron injection layer for efficient and stable organic light emitting diodes, R. Grover et al., J. Luminescence, 146, 53–56 (2014). http://dx.doi.org/10.1016/j.jlumin.2013.09.004.
  10. Upconverted Emission from Pyrene and Di-tert-butylpyrene Using Ir(ppy)3 as Triplet Sensitizer, W. Zhao et al., Phys. Chem. A, 110 (40), 11440–11445 (2006), DOI: 10.1021/jp064261s.
  11. High-efficiency organic electrophosphorescent devices with tri(2-phenylpyridine)iridium doped into electron-transporting materials, C. Adachi et al., Appl. Phys. Lett., 77 (6), 904-906 (2000).
  12. High-efficiency and low-voltage p‐i‐n electrophosphorescent organic light-emitting diodes with double-emission layers, G. He et al., Appl. Phys. Lett. 85, 3911 (2004); http://dx.doi.org/10.1063/1.1812378.

To the best of our knowledge the technical information provided here is accurate. However, Ossila assume no liability for the accuracy of this information. The values provided here are typical at the time of manufacture and may vary over time and from batch to batch.