User:Mtt.cucchi
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(rISC) is a radiationless process involving a transition between two electronic states with different spin spin multiplicity: specifically, it refers to the transition of an electron from a triplet state to a singlet state, as opposed to the intersystem crossing.
Singlet and Triplet states
[edit]See the page about intersystem crossing or about Jablonski diagram.
rISC rate in organic molecules
[edit]Triplets are more stable than singlets. The energy difference between the two states ΔST is given, in organic molecules and metal-organic compounds, by the double of the exchange integral J. J can be calculated as the superposition of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of a given compound, as follows:
.
As the HOMO and LUMO energies are affected by the dielectric environment[1], K can show a strong dependence depending on the materials the compounds are immersed in. Such dependence is particularly strong in case of charge-transfer states i.e. electronic excited states in which the hole and and the electron reside on different moyeties of the molecule.
The rate with which a triplet exciton can undergo a spin-flip and become a singlet is the reverse intersystem crossing rate (Krisc). It is, as a first approximation, a thermally activated process:
where KT is the thermal energy and Kisc is the rate of the intersystem crossing.
Molecules can be designed in such a way to minimize the intgral K, and hence maximize the rISC[2]: in this regards, a photophysical process called thermally-activated delayed fluorescence is of commercial interested in the display industries[3], where it is employed to enhance the efficiency of organic fluoropheres for OLED displays.
In case heavy atoms are present in the molecular structure, the spin-orbit coupling can become predominant and speed up the rISC. This is the case of many phospsorescent molecules.
- ^ Cucchi, Matteo; Matulaitis, Tomas; Kukhta, Nadzeya A.; Grazulevicius, Juozas V.; Reineke, Sebastian; Scholz, Reinhard (2019-10-10). "Influence of the Dielectric Constant around an Emitter on Its Delayed Fluorescence". Physical Review Applied. 12 (4): 044021. doi:10.1103/PhysRevApplied.12.044021. ISSN 2331-7019.
- ^ Uoyama, Hiroki; Goushi, Kenichi; Shizu, Katsuyuki; Nomura, Hiroko; Adachi, Chihaya (2012-12). "Highly efficient organic light-emitting diodes from delayed fluorescence". Nature. 492 (7428): 234–238. doi:10.1038/nature11687. ISSN 0028-0836.
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(help) - ^ "OLED Market reports | OLED-Info". www.oled-info.com. Retrieved 2019-10-26.