Organic Metalloid Emitters for OLED Stability and Color Purity

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Solution Overview

Problem

Existing organic light-emitting diodes (OLEDs) face challenges in achieving high efficiency, color purity, and stability due to limitations in emitter materials, particularly in the blue and green spectral ranges.

Innovation Solution

Development of purely organic molecules incorporating metalloids like B, Si, Sn, and Se, which exhibit emission maxima in the blue, sky-blue, or green spectral range with high photoluminescence quantum yields, enhancing the efficiency and color purity of OLEDs.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If traditional metal complexes are used as emitter materials in OLEDs, then device stability can be improved, but efficiency and color purity in the blue and green spectral ranges are limited

Engineering Contradiction:
Improvedevice stabilityVSAvoidefficiency and color purity
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The patent changes the chemical composition parameters by transitioning from metal-based emitters to purely organic emitters containing specific metalloids (B, Si, Sn, Se, Ge). This parameter change enables achieving both high efficiency (photoluminescence quantum yields of 50% or more) and color purity (emission maxima between 420-520 nm) while maintaining device stability, thereby resolving the contradiction between stability and performance in traditional metal complex emitters

Inventive Principle:
Principle #35Parameter changes

2Ease of manufacture

If purely organic molecules without metalloids are used, then synthesis simplicity is improved, but emission efficiency and color purity in the blue-green range are insufficient

Engineering Contradiction:
Improvesynthesis simplicityVSAvoidemission efficiency and color purity
Core Design Contradiction:
Ease of manufactureVSProductivity

Solution Approach 1:

The patent employs composite material design by combining organic frameworks with specific metalloid elements (B, Si, Sn, Se, Ge) to create purely organic emitter molecules. This composite approach integrates the synthesis advantages of organic molecules with the optical performance benefits of metalloid-containing structures, achieving both ease of manufacture and high emission efficiency (photoluminescence quantum yields of 50% or more) with color purity in the blue-green spectral range

Inventive Principle:
Principle #40Composite materials

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

These organic molecules lead to higher efficiency and stability in OLEDs with improved color purity and emission characteristics, specifically in the blue and green spectral ranges, surpassing traditional emitter materials.

Implementation Method 1

The photoluminescence quantum yields of the organic molecules according to the disclosure are, in particular, 50% or more

Methodology Applied
Scientific EffectPhotoluminescence: Photoluminescence

Implementation Method 2

the organic molecules exhibit emission maxima in the blue, sky-blue or green spectral range

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Data Source

PatentUS20230159568A1Organic molecules for optoelectronic devices
Publication Date: 2023.05.25 SAMSUNG DISPLAY CO LTD
  • US20230159568A1 patent drawing
  • US20230159568A1 patent drawing
  • US20230159568A1 patent drawing

AI summary

The disclosure relates to an organic molecule, in particular for the application in optoelectronic devices. According to the disclosure, the organic molecule has a structure represented by Formula I:In Formula 1,RI, RII, RIII, RIV, RV, RVI, RVII, RVIII, RIX, RX and RXI are each independently selected from the group consisting of:hydrogen, deuterium, halogen,C1-C12-alkyl,wherein optionally one or more hydrogen atoms are each independently substituted by R5,C6-C18-aryl,wherein optionally one or more hydrogen atoms are each independently substituted by R5, andC3-C15-heteroaryl.R5 is independently selected from the group consisting of:hydrogen, deuterium,C1-C12-alkyl, andC6-C18aryl, wherein optionally one or more hydrogen atoms are each independently substituted by C1-C5-alkyl substituents;T, V, W, and X are each independently selected from the group consisting of:C1-C12-alkyl, andC6-C18-aryl,wherein optionally one or more hydrogen atoms are each independently substituted by C1-C5-alkyl substituents.