Energy transfer between Ir(ppy)3 molecules in neat film and concentration quenching of phosphorescence
Source abstract
Abstract
Abstract Numerical calculations are performed for temperature dependences of phosphorescence quantum efficiency and lifetime of Ir(ppy)3 monomer in photo-excited neat film by solving the rate equations for three zero-field splitting substates of the triplet T1 state. In the analysis, we take into account spin–phonon relaxations among the three substates and excitation energy transfer to the excimer state by thermal activation process. Good agreement of the calculated quantum efficiency and lifetime with experimental results is obtained by considering both the excimer formation and triplet–triplet annihilation, e.g., (1) the efficiency increases with decreasing temperature from 300 K to 125 K and then decreases on going from 125 K to 5 K, and (2) the phosphorescence decay curve shows multi-exponential, where the lifetimes increase with decreasing temperature from 300 K. It is suggested that concentration quenching of monomer emission in the neat film is mainly due to the formation of triplet excimer with activation energy of 975 cm−1 and partly triplet–triplet annihilation and polariton pair annihilation.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Lanthanide and Transition Metal Complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (23)
Show source-provided references
1. Holzer · Chem. Phys. · 2005 · 308 · 9310.1016/j.chemphys.2004.07.051 ↗
2. Watanabe · Proc. SPIE · 2000 · 4105 · 17510.1117/12.416892 ↗
3. Baldo · Pure Appl. Chem. · 1999 · 71 · 209510.1351/pac199971112095 ↗
4. Peng · SID 05 Digest · 2005 · 106610.1889/1.2036183 ↗
5. Goushi · Jpn. J. Appl. Phys. · 2004 · 43 · L93710.1143/JJAP.43.L937 ↗
6. Kobayashi · Jpn. J. Appl. Phys. · 2005 · 44 · 196610.1143/JJAP.44.1966 ↗
7. Tsuboi · Thin Solid Films · 2006 · 499 · 30610.1016/j.tsf.2005.07.020 ↗
8. Namdas · J. Phys. Chem. · 2004 · 108 · 157010.1021/jp035664k ↗
9. Tsuzuki · Jpn. J. Appl. Phys. · 2005 · 44 · 415110.1143/JJAP.44.4151 ↗
10. D’Andrade · Chem. Phys. · 2002 · 286 · 32110.1016/S0301-0104(02)00921-7 ↗
11. Sapunov · Opt. Spectrosc. · 1980 · 49 · 152
12. Sapunov · Opt. Spectrosc. · 2000 · 88 · 35910.1134/1.626802 ↗
13. Birks · Rep. Prog. Phys. · 1975 · 38 · 90310.1088/0034-4885/38/8/001 ↗
14. Takemura · J. Am. Chem. Soc. · 1976 · 98 · 220510.1021/ja00424a033 ↗
15. Kalinowski · Chem. Phys. · 2004 · 297 · 3910.1016/j.chemphys.2003.09.041 ↗
16. Finkenzeller · Chem. Phys. Lett. · 2003 · 377 · 29910.1016/S0009-2614(03)01142-4 ↗
17. Tsuboi · Jpn. J. Appl. Phys. · 2005 · 44 · 59110.1143/JJAP.44.591 ↗
18. Bhasikuttan · J. Am. Chem. Soc. · 2003 · 124 · 839810.1021/ja026135h ↗
19. MaCusker · Acc. Chem. Res. · 2003 · 36 · 87610.1021/ar030111d ↗
20. Tanaka · Jpn. J. Appl. Phys. · 2004 · 43 · L160110.1143/JJAP.43.L1601 ↗
21. Akimoto · J. Lumin. · 2007 · 122–123 · 44010.1016/j.jlumin.2006.01.200 ↗
22. Bansal · Chem. Phys. · 2006 · 330 · 11810.1016/j.chemphys.2006.08.002 ↗
23. Holzer · Synth. Metal · 2002 · 125 · 34310.1016/S0379-6779(01)00473-8 ↗