Organic light-emitting device, and light-emitting material and compound used therefor
US-2015105564-A1 · Apr 16, 2015 · US
US2016149139A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016149139-A1 |
| Application number | US-201414553676-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 25, 2014 |
| Priority date | Nov 25, 2014 |
| Publication date | May 26, 2016 |
| Grant date | — |
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A composition formed of a mixture of two compounds having similar thermal evaporation properties that are pre-mixed into an evaporation source that can be used to co-evaporate the two compounds into an emission layer in OLEDs via vacuum thermal evaporation process is disclosed. The first and second compounds can have an evaporation temperature T 1 and T 2 , respectively, of 150 to 350° C., and the absolute value of T 1 −T 2 can be less than 20° C. The first compound can have a concentration C 1 in the mixture and a concentration C 2 in a film formed by evaporating the mixture in a vacuum deposition tool at a constant pressure between 1×10 −6 Torr to 1×10 −9 Torr, at a 2 Å/sec deposition rate on a surface positioned at a predefined distance away from the mixture being evaporated, where the absolute value of (C 1 −C 2 )/C 1 is less than 5%.
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1 . A composition comprising, a mixture of a first compound and a second compound; wherein the first compound has a different chemical structure than the second compound; wherein the mixture of the first compound and the second compound is capable of functioning as a delayed fluorescent system in an organic light emitting device at room temperature; wherein the first compound has an evaporation temperature T 1 of 150 to 350° C.; wherein the second compound has an evaporation temperature T 2 of 150 to 350° C.; wherein absolute value of T 1 −T 2 is less than 20° C.; wherein the first compound has a concentration C 1 in said mixture and a concentration C 2 in a film formed by evaporating the mixture in a vacuum deposition tool at a constant pressure between 1×10 −6 Torr to 1×10 −9 Torr, at a 2 Å/sec deposition rate on a surface positioned at a predefined distance away from the mixture being evaporated; and wherein absolute value of (C 1 −C 2 )/C 1 is less than 5%. 2 - 3 . (canceled) 4 . The composition of claim 1 , wherein the first compound has a vapor pressure of P 1 at T 1 at 1 atm, and the second compound has a vapor pressure of P 2 at T 2 at 1 atm; and wherein the ratio of P 1 /P 2 is within the range of 0.90:1 to 1.10:1. 5 - 7 . (canceled) 8 . The composition of claim 1 , wherein the second compound is capable of functioning as a host in an organic light emitting device at room temperature. 9 - 10 . (canceled) 11 . The composition of claim 1 , wherein the second compound comprises at least one chemical group selected from the group consisting of anthracence, naphthylene, phenanthrene, triphenylene, carbazole, dibenzothiphene, dibenzofuran, dibenzoselenophene, aza-triphenylene, aza-carbazole, aza-dibenzothiophene, aza-dibenzofuran, and aza-dibenzoselenophen. 12 . (canceled) 13 . The composition of claim 1 , wherein the composition further comprises a third compound, wherein the third compound has a different chemical structure than the first and second compounds, wherein the third compound has an evaporation temperature T 3 of 150 to 350° C., and wherein absolute value of T 1 −T 3 is less than 20° C. 14 . The composition of claim 1 , wherein the composition is in liquid form at a temperature less than the lesser of T 1 and T 2 . 15 . The composition of claim 1 , wherein the delayed fluorescent system is a P-type delayed fluorescent system. 16 . The composition of claim 15 , wherein the first compound comprises at least one chemical group selected from the group consisting of pyrene, fluoranthene, chrysene, benzofluorene, and stilbene. 17 . The composition of claim 15 , wherein the first compound is selected from the group consisting of: 18 . The composition of claim 17 , wherein the second compound is selected from the group consisting of:
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