TADF Organic Compound for High-Efficiency Light Emission

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Solution Overview

Problem

Current organic light-emitting devices face challenges in achieving high emission efficiency and low power consumption, particularly in exhibiting delayed fluorescence and thermally activated delayed fluorescence (TADF) for improved light emission performance.

Innovation Solution

Development of an organic compound with a specific molecular structure, represented by General Formula (G1) to (G5), which has a small difference between the lowest singlet and triplet excited levels, facilitating efficient TADF light emission and incorporating this compound into a light-emitting device structure with a bipolar host material for enhanced emission efficiency.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If conventional organic compounds are used in light-emitting devices, then device structure can be simplified, but emission efficiency is insufficient and power consumption is high

Engineering Contradiction:
Improvedevice structure simplicityVSAvoidemission efficiency
Core Design Contradiction:
Ease of manufactureVSLoss of energy

Solution Approach 1:

The patent modifies molecular parameters of organic compounds by adjusting the difference between singlet and triplet excited levels (ΔEST) to be 0.05 eV or less, and controlling HOMO-LUMO energy gaps. This parameter optimization enables efficient TADF while maintaining device structure simplicity, resolving the contradiction between ease of manufacture and emission efficiency.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs composite material strategies by combining TADF-emitting organic compounds with bipolar host materials in the light-emitting layer. This composite approach enhances emission efficiency through synergistic effects while preserving the relative simplicity of the device structure, addressing both manufacturing ease and energy loss concerns.

Inventive Principle:
Principle #40Composite materials

2Loss of energy

If organic compounds with small ΔEST are designed to achieve TADF, then emission efficiency improves, but molecular structure complexity increases

Engineering Contradiction:
Improveemission efficiencyVSAvoidmolecular structure complexity
Core Design Contradiction:
Loss of energyVSDevice complexity

Solution Approach 1:

The patent achieves TADF by optimizing specific molecular parameters: controlling ΔEST ≤ 0.05 eV and adjusting HOMO-LUMO energy gaps. Rather than complex structural modifications, this parameter-based approach enables efficient TADF with relatively simple molecular frameworks, reducing the complexity burden while improving emission efficiency.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent extracts and emphasizes the critical parameter (ΔEST) from complex molecular structure considerations. By focusing on this key parameter and decoupling it from overall molecular complexity, the invention achieves TADF efficiency without requiring elaborate molecular architectures, thus resolving the contradiction between emission efficiency and structural complexity.

Inventive Principle:
Principle #2Taking out (Extraction)

3Device complexity

If conventional fluorescent emission is used, then device structure is simple, but power consumption is high

Engineering Contradiction:
Improvedevice structure simplicityVSAvoidpower consumption
Core Design Contradiction:
Device complexityVSUse of energy by moving object

Solution Approach 1:

The patent transitions from conventional fluorescent emission to TADF by changing the energy level parameters (ΔEST ≤ 0.05 eV). This parameter modification enables utilization of both singlet and triplet excitons for light emission, dramatically improving power efficiency while maintaining simple device structure, thus resolving the contradiction between structural simplicity and power consumption.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent converts the previously harmful triplet excitons (which caused energy loss in fluorescent devices) into beneficial light-emitting species through TADF mechanism. By enabling reverse intersystem crossing from triplet to singlet state, the invention transforms energy waste into useful light emission, reducing power consumption while keeping device structure simple.

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

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 organic compound efficiently exhibits TADF light emission with favorable emission efficiency and low power consumption, leading to improved performance in light-emitting devices with extended transient lifetimes and high external quantum efficiency.

Implementation Method 1

an organic compound that easily exhibits delayed fluorescence and thermally activated delayed fluorescence (TADF)

Methodology Applied
Scientific EffectThermally activated delayed fluorescence (TADF):

Implementation Method 2

Light-emitting devices (organic EL devices) including organic compounds and utilizing electroluminescence (EL) have been put into practical use. Carriers are injected by application of voltage to the element, and recombination energy of the carriers is used, whereby light emission can be obtained from the light-emitting material.

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Data Source

PatentUS20230129057A1Organic Compound, Light-Emitting Device, Electronic Device, Electronic Apparatus, Light-Emitting Apparatus, and Lighting Apparatus
Publication Date: 2023.04.27 SEMICON ENERGY LAB CO LTD
  • US20230129057A1 patent drawing
  • US20230129057A1 patent drawing
  • US20230129057A1 patent drawing

AI summary

An organic compound that easily exhibits thermally activated delayed fluorescence (TADF) is provided. An organic compound represented by General Formula (G1) is provided. In General Formula (G1), R1 to R8 are each independently any one of hydrogen, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 7 carbon atoms, and a substituted or unsubstituted diarylamino group; at least one of R1 to R8 is a substituted or unsubstituted diarylamino group; a is a substituted or unsubstituted phenylene group; n is an integer of 0 to 4; and A represents a substituted or unsubstituted benzofuropyrimidine skeleton or benzothienopyrimidine skeleton.