Purely Organic TADF Molecules for OLED Efficiency and Stability

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Solution Overview

Problem

Existing optoelectronic devices, such as OLEDs, face challenges in achieving high efficiency and stability due to the limitations of metal complexes used in emission materials, particularly in the blue, sky-blue, or green spectral range.

Innovation Solution

Development of purely organic molecules without metal ions, exhibiting thermally activated delayed fluorescence (TADF) with emission maxima between 420 nm and 520 nm, and high photoluminescence quantum yields, specifically designed for use in OLEDs to enhance device efficiency and stability.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If metal complexes are used as emission materials in OLEDs, then device efficiency can be improved, but device stability deteriorates

Engineering Contradiction:
Improvedevice efficiencyVSAvoiddevice stability
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent removes metal ions from the emission material structure, extracting the harmful component (metal) while retaining the desired photoluminescent properties through purely organic molecular design. This extraction principle directly resolves the contradiction by eliminating the source of instability while maintaining efficiency through organic TADF mechanisms.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent changes the fundamental parameter of material composition from metal-containing complexes to purely organic molecules. This parameter change enables the system to achieve both high efficiency and stability by utilizing thermally activated delayed fluorescence (TADF) in organic compounds, which avoids the degradation issues associated with metal complexes while maintaining high photoluminescence quantum yields.

Inventive Principle:
Principle #35Parameter changes

2Reliability

If purely organic molecules are used instead of metal complexes, then device stability is improved, but achieving high efficiency becomes more difficult

Engineering Contradiction:
Improvedevice stabilityVSAvoiddevice efficiency
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The patent changes the photophysical mechanism parameter from conventional fluorescence or phosphorescence to thermally activated delayed fluorescence (TADF). This parameter change enables purely organic molecules to achieve high efficiency by utilizing reverse intersystem crossing and triplet state utilization, which were previously only achievable through metal complex phosphorescence.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs composite molecular structures combining electron-donating and electron-withdrawing moieties in specific configurations. This composite approach creates intramolecular charge transfer states that enable efficient TADF in purely organic systems, resolving the efficiency challenge while maintaining the stability advantage of metal-free materials.

Inventive Principle:
Principle #40Composite materials

3Ease of manufacture

If conventional emission materials are used, then manufacturing processes are simpler, but device lifetime is reduced

Engineering Contradiction:
Improvemanufacturing simplicityVSAvoiddevice lifetime
Core Design Contradiction:
Ease of manufactureVSDuration of action of stationary object

Solution Approach 1:

The patent extracts metal components from the emission material, simplifying the manufacturing process by eliminating complex metal complex synthesis and purification steps. The purely organic molecules can be synthesized through standard organic chemistry techniques, making the manufacturing process simpler while simultaneously improving device lifetime through enhanced material stability.

Inventive Principle:
Principle #2Taking out (Extraction)

4Ease of manufacture

If metal complexes are used for blue, sky-blue, or green emission, then color characteristics can be achieved, but material degradation increases

Engineering Contradiction:
Improvecolor characteristicsVSAvoidmaterial degradation
Core Design Contradiction:
Ease of manufactureVSObject-generated harmful factors

Solution Approach 1:

The patent changes the emission mechanism parameter to TADF in purely organic molecules, which enables precise control over emission color (blue, sky-blue, green) through molecular structure design while avoiding the degradation pathways associated with metal complexes. The organic molecules exhibit enhanced photostability and resistance to degradation while maintaining the desired spectral properties.

Inventive Principle:
Principle #35Parameter changes

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The new organic molecules lead to higher efficiency and stability in OLEDs with comparable color characteristics, offering improved performance in optoelectronic devices by utilizing TADF and specific spectral emission ranges.

Implementation Method 1

The molecules according to the invention exhibit in particular thermally activated delayed fluorescence (TADF)

Methodology Applied
Scientific EffectThermally activated delayed fluorescence (TADF): Photoluminescence

Implementation Method 2

The photoluminescence quantum yields of the organic molecules according to the invention are, in particular, 20 % or more

Methodology Applied
Scientific EffectPhotoluminescence: Photoluminescence

Data Source

PatentEP3694850B1Organic molecules for use in optoelectronic devices
Publication Date: 2023.10.11 SAMSUNG DISPLAY CO LTD
  • EP3694850B1 patent drawingFigure 1~2
  • EP3694850B1 patent drawingFigure 3~4
  • EP3694850B1 patent drawingFigure 5~6

AI summary

CYN232WO15.10.2018 cynora GmbH83DARANi Summary The invention relates to an organic compound, in particularfor the usein optoelectronic devices.According to the invention, the organicmoleculehas -onefirst chemical moiety witha structure of formula I, Formula I and -two second chemical moieties, each at each occurrence independently from another witha structure of formula II, Formula II wherein the first chemical moiety is linked to each of the two second chemical moietiesvia a single bond; # represents the binding site of a single bond linking asecond chemical moietyto the first chemical moiety; $represents the binding site of a single bond linking the first chemical moietyto the second chemical moiety; §represents the binding site of a single bond linking the first chemical moietyto the second chemical moiety;and Q is either N or CR II