Purely Organic Emitters for OLED Efficiency and Stability

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Solution Overview

Problem

Current optoelectronic devices, such as OLEDs, face challenges with metal complexes that limit efficiency and stability, particularly in achieving high photoluminescence quantum yields and thermal activated delayed fluorescence (TADF) in blue, sky-blue, or green spectral ranges.

Innovation Solution

Development of purely organic molecules without metal ions, specifically designed with certain chemical moieties and structures that exhibit emission maxima between 420 nm and 520 nm, with high photoluminescence quantum yields and TADF properties, enhancing device efficiency and stability.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If metal complexes are used as emitter 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 emitter material composition entirely, extracting the harmful element (metal) while retaining the desired photoluminescent properties through purely organic molecular structures. This resolves the contradiction by eliminating the source of instability while maintaining efficiency through carefully designed organic emitters with appropriate HOMO-LUMO energy levels and radiative decay pathways.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent employs composite molecular structures combining electron-donating moieties (such as carbazole, triphenylamine) with electron-accepting moieties (such as pyridine, pyrimidine) to create purely organic emitter materials. This composite approach at the molecular level achieves both high efficiency through effective charge transfer and long-lived excited states, while maintaining stability by avoiding metal degradation pathways.

Inventive Principle:
Principle #40Composite materials

2Reliability

If purely organic molecules are used instead of metal complexes, then device stability is improved, but photoluminescence quantum yield deteriorates

Engineering Contradiction:
Improvedevice stabilityVSAvoidphotoluminescence quantum yield
Core Design Contradiction:
ReliabilityVSLoss of energy

Solution Approach 1:

The patent systematically adjusts molecular parameters including HOMO-LUMO energy gap, radiative decay rate, and non-radiative decay pathways by modifying molecular structure. By controlling the energy gap between S1 and S0 states and optimizing orbital overlap, the patent achieves high photoluminescence quantum yields in purely organic molecules while maintaining stability, directly resolving this contradiction.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent introduces specific functional groups and molecular moieties with localized electron-donating or electron-accepting properties at specific positions in the molecular structure. This local optimization of electronic properties enhances radiative decay rates and photoluminescence quantum yield in specific regions of the molecule without compromising overall molecular stability.

Inventive Principle:
Principle #3Local quality

3Ease of manufacture

If emission maxima are targeted in blue spectral range (420-520 nm), then color performance is improved, but achieving high photoluminescence quantum yield becomes more difficult

Engineering Contradiction:
Improvecolor performanceVSAvoidphotoluminescence quantum yield
Core Design Contradiction:
Ease of manufactureVSLoss of energy

Solution Approach 1:

The patent precisely controls the HOMO-LUMO energy gap parameter to correspond to blue emission wavelengths (420-520 nm) while simultaneously optimizing radiative and non-radiative decay rates. By adjusting molecular structure to achieve specific energy levels and orbital configurations, the patent accomplishes both desired blue color performance and high photoluminescence quantum yield, resolving this contradiction.

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 improve the efficiency and stability of OLEDs by achieving higher photoluminescence quantum yields and maintaining comparable color performance, with specific emission ranges and TADF capabilities.

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 organic molecules exhibit emission maxima in the blue, sky-blue or green spectral range. The organic molecules exhibit in particular emission maxima between 420 nm and 520 nm

Methodology Applied
Scientific EffectPhotoluminescence: Photoluminescence

Data Source

PatentEP3450429B1Organic molecules, in particular for use in optoelectronic devices
Publication Date: 2020.02.19 CYNORA
  • EP3450429B1 patent drawingFigure 1~2
  • EP3450429B1 patent drawing
  • EP3450429B1 patent drawing

AI summary

The invention relates to an organic compound, in particular for the use in optoelectronic devices. According to the invention, the organic compound has - a first chemical moiety with a structure of formula I, and - two second chemical moieties, each independently from another with a structure of formula II, wherein the first chemical moiety is linked to each of the two second chemical moieties via a single bond; wherein T, V, X, Y is each independently form each other the binding site of a single bond linking the first chemical moiety to one of the two second chemical moieties or is R2; RX is selected from the group consisting of CF3 and CN; wherein exactly two substituents selected of the group consisting of T, V, X and Y represent the binding sites of a single bond linking the first chemical moiety to one of the two second chemical moieties.