Compounds and Organic Electronic Devices
US-2017317285-A1 · Nov 2, 2017 · US
US2025143175A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2025143175-A1 |
| Application number | US-202418774780-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 16, 2024 |
| Priority date | Oct 27, 2023 |
| Publication date | May 1, 2025 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
An optoelectronic device includes a first electrode, a second electrode facing the first electrode, and a photoactive layer between the first electrode and the second electrode, where the photoactive layer may include an acceptor satisfying Expression 1 and a donor having a maximum absorption wavelength of about 600 nm to about 750 nm, and Expression 2 may be satisfied: 3 eV ≤ E LUMO A - E HOMO A ≤ 4 eV Expression 1 0.05 ≤ ( E LUMO D - E LUMO A ) / ( E LUMO D - E HOMO D ) ≤ 0.5 . Expression 2
Opening claim text (preview).
What is claimed is: 1 . An optoelectronic device comprising: a first electrode; a second electrode facing the first electrode; and a photoactive layer between the first electrode and the second electrode, wherein the photoactive layer comprises an acceptor satisfying Expression 1 and a donor having a maximum absorption wavelength of about 600 nm to about 750 nm, and Expression 2 is satisfied: 3 eV ≤ E LUMO A - E HOMO A ≤ 4 eV Expression 1 0.05 ≤ ( E LUMO D - E LUMO A ) / ( E LUMO D - E HOMO D ) ≤ 0.5 Expression 2 in Expressions 1 and 2, E D LUMO representing a lowest unoccupied molecular orbital (LUMO) energy level of the donor, E D HOMO representing a highest occupied molecular orbital (HOMO) energy level of the donor, E A LUMO representing a LUMO energy level of the acceptor, and E A HOMO representing a HOMO energy level of the acceptor. 2 . The optoelectronic device of claim 1 , wherein the donor satisfies Expression 3: 1. eV ≤ E LUMO D - E HOMO D ≤ 2.5 eV Expression 3 in Expression 3, E D LUMO and E D HOMO each being the same as described in Expression 2. 3 . The optoelectronic device of claim 1 , wherein Expression 4 is further satisfied: E LUMO A ≤ E LUMO D Expression 4 in Expression 4, E D LUMO and E A LUMO each being the same as described in Expressions 1 and 2. 4 . The optoelectronic device of claim 1 , wherein Expression 5 is further satisfied: E HOMO A ≤ E HOMO D Expression 5 in Expression 5, E D HOMO and E A HOMO each being the same as described in Expressions 1 and 2. 5 . The optoelectronic device of claim 1 , wherein the acceptor does not comprise a fullerene-based compound. 6 . The optoelectronic device of claim 1 , wherein the acceptor does not comprise a 5-membered ring. 7 . The optoelectronic device of claim 1 , wherein the acceptor is transparent in a visible light region. 8 . The optoelectronic device of claim 1 , wherein the acceptor is represented by Formula 1: wherein, in Formula 1, X 1 to X 4 are each independently O, S, or Se, Z 1 is O or N(R 5 ), Z 2 is O or N(R 6 ), R 1 to R 6 are each independently hydrogen, deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, a C 1 -C 60 alkyl group unsubstituted or substituted with at least one R 10a , a C 2 -C 60 alkenyl group unsubstituted or substituted with at least one R 10a , a C 2 -C 60 alkynyl group unsubstituted or substituted with at least one R 10a , a C 1 -C 60 alkoxy group unsubstituted or substituted with at least one R 10a , a C 3 -C 60 carbocyclic group unsubstituted or substituted with at least one R 10a , a C 1 -C 60 heterocyclic group unsubstituted or substituted with at least one R 10a , a C 6 -C 60 aryloxy group unsubstituted or substituted with at least one R 10a , a C 6 -C 60 arylthio group unsubstituted or substituted with at least one R 10a , a C 7 -C 60 arylalkyl group unsub
Package configurations · CPC title
Interrelation of parameters between multiple constituent active layers or sublayers, e.g. HOMO values in adjacent layers · CPC title
Active-matrix OLED [AMOLED] displays · CPC title
OLEDs integrated with touch screens · CPC title
comprising organic-organic junctions, e.g. donor-acceptor junctions · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.