IP Library Granted Patent US 12,312,522
Granted Patent B2
US 12,312,522 · App. 15/128,099 · Granted May 27, 2025

Organic optoelectronic apparatus

Inventors: Dominik Pentlehner (Regensburg, DE); Andreas Rausch (Regensburg, DE)
Assignee: Pictiva Displays International Limited
C09K11/06H10K50/125H10K50/13H10K50/131H10K85/611H10K85/615H10K85/622H10K85/6565H10K85/6572C09K2211/1007C09K2211/1011C09K2211/1029C09K2211/1048H10K50/11H10K50/15H10K50/16H10K50/17H10K50/171H10K85/633H10K85/654H10K2101/10
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Quick Facts
Patent No.
US 12,312,522
App. No.
15/128,099
Granted
May 27, 2025
Kind
B2
Abstract

The invention relates to an organic optoelectronic apparatus comprising: a first electrode ( 2 ), a radiation-emitting region ( 4 ) arranged between the first and second electrodes, and a second electrode ( 9 ), wherein the first and second electrodes can inject charge carriers of different polarity into the radiation-emitting region, wherein the radiation-emitting region ( 4 ) has a dual emitter and a further emitter, wherein the further emitter is transferred by the charge carrier into an electronically excited state and, on the transition into the basic electronic state from this electronically excited state, emits radiation, and wherein the dual emitter has a first electronically excited state and a second electronically excited state, which can be reached from the first electronically excited state by intramolecular proton transfer or intramolecular charge transfer, and the dual emitter has an emission starting from the second electronically excited state into a second basic state. The radiation emitted by this apparatus has an improved CRI value owing to the simultaneous use of a dual emitter and a further emitter.

Claims (18)

1. An organic optoelectronic apparatus for the emission of white light, comprising:

a first electrode,

a second electrode,

a radiation-emitting region arranged between the first and second electrode,

wherein the first and second electrodes can inject charge carriers of different polarity into the radiation-emitting region,

wherein the radiation-emitting region comprises two different dual emitters,

wherein the radiation-emitting region comprises a first radiation-emitting layer and a second radiation-emitting layer and each of the radiation-emitting layers comprises one dual emitter,

wherein each one of the dual emitters comprises a first electronically excited state and a second electronically excited state which can be achieved from the first electronically excited state,

wherein the dual emitters each comprise an emission starting from the first electronically excited state and second electronically excited state into a first basic electronic state and a second basic electronic state respectively,

wherein each of the dual emitters comprises a molecule that is selected from one of the following general formulas:

wherein R 1 to R 15 are hydrogen, alkyl, alkenyl groups, long-chain alkyl, alkoxy, long-chain alkoxy, cycloalkyl, haloalkyl, aryl, arylenes, haloaryl, heteroaryl, heteroarylenes, heterocycloalkylenes, heterocycloalkyl, haloheteroaryl, alkenyl, haloalkenyl, alkinyl, haloalkinyl, ketoaryl, haloketoaryl, ketoheteroaryl, ketoalkyl, haloketoalkyl, ketoalkenyl, haloketoalkenyl, or part of a cyclic, aromatic, or heteroaromatic system and

wherein a superimposition of the radiations from each of the radiation-emitting layers produces white light.

2. The organic optoelectronic apparatus according to claim 1 , wherein each dual emitter of the two different dual emitters in the radiation-emitting region emits fluorescent radiation.

3. The organic optoelectronic apparatus according to claim 1 , wherein for each one of the dual emitters, an intramolecular charge transfer from the first electronically excited state to the second electronically excited state is effected more rapidly than a radiation-emitting decomposition starting from the first electronically excited state to a first basic electronic state.

4. The organic optoelectronic apparatus according to claim 1 , wherein a transition starting from the second basic electronic state of each one of the dual emitters to a first basic electronic state is more rapid than a radiating transition starting from the second electronically excited state to the second basic electronic state.

5. The organic optoelectronic apparatus according to claim 1 , wherein the first radiation-emitting layer and the second radiation-emitting layer are separated from one another by an intermediate layer that comprises either a charge generation layer or a charge carrier-transporting layer.

6. The organic optoelectronic apparatus according to claim 1 , wherein each one of the dual emitters comprises molecules of the following general formula:

7. The organic optoelectronic apparatus according to claim 1 , wherein each one of the dual emitters comprises molecules of the following general formula:

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2020
From: OSRAM OLED GMBH
To: DOLYA HOLDCO 5 LIMITED
Reel/Frame 053464/0374 →
CORRECTIVE ASSIGNMENT TO CORRECT THE 11/658.772 REPLACED 11/658.772 PROPERTY NUMBERS PREVIOUSLY RECORDED AT REEL: 053464 FRAME: 0395. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Aug 11, 2020
From: DOLYA HOLDCO 5 LIMITED
To: PICTIVA DISPLAYS INTERNATIONAL LIMITED
Reel/Frame 053464/0395 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 11, 2017
From: PENTLEHNER, DOMINIK; RAUSCH, ANDREAS
To: OSRAM OLED GMBH
Reel/Frame 042347/0511 →
Priority Claims (1)
DE 102014103943.2 · Mar 21, 2014 · national
Continuity (1)
Related Publication 20170125695A1 · May 4, 2017
References Cited (24)
US 4647400A · Dubroca · 1987 [cited by examiner]
US 6869695B2 · Thompson et al. · 2005 [cited by applicant]
US 20040032205A1 · Hack · 2004 [cited by examiner]
US 20100301317A1 · Nowatari · 2010 [cited by examiner]
US 20120046472A1 · Park et al. · 2012 [cited by applicant]
US 20120153266A1 · Thompson et al. · 2012 [cited by applicant]
US 20170324007A1 · Pentlehner · 2017 [cited by examiner]
DE 102011076791A1 · 2012 [cited by applicant]
WO 2004005280A1 · 2004 [cited by applicant]
WO 2010066245A1 · 2010 [cited by applicant]
Baranoff et al. Dalton Trans., 2015, 44, 8318-8329 (Year: 2015). [cited by examiner]
Hu et al. Synthetic Metals 137 (2003) 1123-1124 (Year: 2003). [cited by examiner]
Park et al. J. Am. Chem. Soc. 2009, 131, 14043-14049 (Year: 2009). [cited by examiner]
Kim, S. et al., “White Luminescence from Polymer Thin Films Containing Excited-State Intramolecular Proton-Transfer Dyes”, WILEY-VCH, Adv. Mater., vol. 17, 2005, pp. 2077-2082. [cited by applicant]
Kim, S. H. et al., “Organic Light-Emitting Diodes with a White-Emitting Molecule: Emission Mechanism and Device Characteristics”, WILEY-VCH, Adv. Funct. Mater., vol. 21, 2011, pp. 644-651. [cited by applicant]
Park, S. et al., “A White-Light Emitting Molecule: Frustrated Energy Transfer between Constituent Emitting Centers”, J. Am. Chem. Soc., vol. 131, 2009, pp. 14043-14049. [cited by applicant]
Kalinowski, J. et al., “Mixing of Excimer and Exciplex Emission: A New Way to Improve White Light Emitting Organic Electrophosphorescent Diodes”, WILEY-VCH, Adv. Mater., vol. 19, 2007, pp. 4000-4005. [cited by applicant]
Kamtekar, K. T. et al., Recent Advances in White Organic Light-Emitting Materials and Devices (WOLEDs), WILEY-VCH, Adv. Mater., vol. 22, 2010, pp. 572-582. [cited by applicant]
Park, S. Y. et al., “25.1: Invited Paper: White-Emitting Molecule: “Molecular Pixel” from Covalently Bonded Sub-Pixels”, SID 10 Digest, 2010, pp. 350-352. [cited by applicant]
Zhao, J. et al., “Excited State Intramolecular Proton Transfer (ESIPT): from Principal Photophysics to the Development of New Chromophores and Applications in Fluorescent Molecular Probes and Luminescent Materials”, Phy… [cited by applicant]
Zhou, G. et al., “Duplicating “Sunlight” from Simple WOLEDs for Lighting Applications”, The Royal Society of Chemistry, Chem. Commun., 2009, pp. 3574-3576. [cited by applicant]
Grabowski, Z. et al., “Structural Changes Accompanying Intramolecular Electron Transfer: Focus on Twisted Intramolecular Charge-Transfer States and Structures”, Chem. Rev., vol. 103, 2003, pp. 3899-4031. [cited by applicant]
Jou, J-H et al., “High-Efficiency, Very High Color Rendering White Organic Light-Emitting Diode with a High Triplet Interlayer”, J. Mater. Chem., vol. 21, 2011, pp. 18523-18526. [cited by applicant]
Kwon, J. E. et al., “Advanced Organic Optoelectronic Materials: Harnessing Excited-State Intramolecular Proton Transfer (ESIPT) Process”, Adv. Mater., 2011, vol. 23, pp. 3615-3642. [cited by applicant]