TADF Organic Electroluminescent Material Design

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Solution Overview

Problem

The existing organic electroluminescent materials, particularly heat activated delayed fluorescence (TADF) materials, have limited choices and performance, which hinders their application in organic light-emitting diodes (OLEDs) due to high production costs and limited luminous efficiency.

Innovation Solution

A new organic electroluminescent material with a specific chemical formula is introduced, featuring compounds that have a controlled energy difference between singlet and triplet excited states, enabling efficient reverse intersystem crossing and improved luminous efficiency without the need for expensive metal complexes, thus enhancing the performance and reducing manufacturing costs.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If existing TADF materials are used, then production cost is reduced compared to phosphorescent materials, but luminous efficiency and performance are limited

Engineering Contradiction:
Improveproduction costVSAvoidluminous efficiency
Core Design Contradiction:
Ease of manufactureVSProductivity

Solution Approach 1:

The patent modifies molecular parameters by adjusting the energy difference between singlet and triplet states (ΔEST) through systematic changes in molecular structure, including varying electron-donating and electron-withdrawing groups, to optimize reverse intersystem crossing efficiency and achieve high luminous efficiency without using expensive heavy metal complexes

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs composite molecular structures combining electron-donating units (e.g., carbazole, triphenylamine) with electron-withdrawing units (e.g., pyridine, pyrimidine) to create TADF materials with optimized charge transfer characteristics and enhanced luminous efficiency while maintaining cost-effectiveness

Inventive Principle:
Principle #40Composite materials

2Productivity

If the energy difference between singlet and triplet states is reduced to enable efficient reverse intersystem crossing, then luminous efficiency improves, but the design complexity of molecular structure increases

Engineering Contradiction:
Improveluminous efficiencyVSAvoidmolecular structure design
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent divides the molecular structure into distinct functional segments: electron-donating units (e.g., carbazole, triphenylamine), electron-withdrawing units (e.g., pyridine, pyrimidine, triazine), and connecting units, allowing independent optimization of each segment to control ΔEST and facilitate reverse intersystem crossing while managing structural complexity

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent applies local quality by strategically placing specific functional groups at particular positions in the molecular structure to create localized electron density variations that optimize charge transfer and control the energy gap between singlet and triplet states, thereby improving luminous efficiency

Inventive Principle:
Principle #3Local quality

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 material improves luminous efficiency and reduces production costs, offering a broader range of applications for TADF materials in OLEDs by optimizing the energy difference between singlet and triplet states, leading to enhanced performance in organic optoelectronic devices.

Implementation Method 1

enabling efficient reverse intersystem crossing and improved luminous efficiency

Methodology Applied
Scientific EffectReverse intersystem crossing:

Implementation Method 2

Organic electroluminescent material

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Data Source

PatentUS10538700B2Organic electroluminescent material and organic optoelectronic device
Publication Date: 2020.01.21 WUHAN TIANMA MICRO ELECTRONICS CO LTD
  • US10538700B2 patent drawing
  • US10538700B2 patent drawing
  • US10538700B2 patent drawing

AI summary

A compound and an organic optoelectronic device are provided. The compound has the following chemical formula (I):In the chemical formula (I), R1 to R10 are independently selected from hydrogen, deuterium, C1 to C30 alkyl, C1 to C30 heteroatom-substituted alkyl, C6 to C30 aryl, and C2 to C30 heteroaryl; X1 is selected from O, S, substituted or unsubstituted imino, substituted or unsubstituted methylene, and substituted or unsubstituted silylene. A substituent is selected from hydrogen, deuterium, C1 to C30 alkyl, C1 to C30 heteroatom-substituted alkyl, C6 to C30 aryl, and C2 to C30 heteroaryl. A1 and A2 are chemical groups independently represented by the following chemical formula (II),