Polycyclic Compound with Benzimidazole Groups for OLED Efficiency

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Solution Overview

Problem

Current organic electroluminescence devices face challenges in achieving high efficiency and long service life while maintaining low driving voltage, particularly in the development of thermally activated delayed fluorescence (TADF) materials.

Innovation Solution

Incorporating a polycyclic compound with two aromatic 6-membered rings linked by a single bond and substituted with benzimidazole groups, which are substituted at the ortho-position, into the organic electroluminescence device's emission or electron transport layers, enhancing the lowest triplet excitation energy level to 2.8 eV or more.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If conventional organic electroluminescence materials are used, then device structure is simple, but luminous efficiency and service life are insufficient

Engineering Contradiction:
Improveluminous efficiencyVSAvoidservice life
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent modifies the molecular structure parameters of the organic compound by introducing a specific polycyclic framework with two aromatic six-membered rings connected by a single bond, and substituting benzimidazole groups at ortho-positions. This structural parameter change increases the lowest triplet excitation energy level to 2.8 eV or more, which directly improves both luminous efficiency and service life characteristics of the electroluminescence device.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs a composite molecular structure combining polycyclic aromatic hydrocarbon frameworks with heterocyclic benzimidazole groups. This composite approach creates a material that leverages the high triplet energy levels of the polycyclic core while incorporating the electron transport and stability benefits of the benzimidazole substituents, achieving simultaneous improvement in efficiency and device lifetime.

Inventive Principle:
Principle #40Composite materials

2Productivity

If thermally activated delayed fluorescence materials are developed to improve efficiency and service life, then luminous efficiency and service life are enhanced, but driving voltage increases

Engineering Contradiction:
Improveluminous efficiencyVSAvoiddriving voltage
Core Design Contradiction:
ProductivityVSPower

Solution Approach 1:

The patent optimizes the energy level parameters by controlling the lowest triplet excitation energy (T1) to be 2.8 eV or more through specific molecular design. This parameter optimization enables the material to achieve high luminous efficiency via thermally activated delayed fluorescence while maintaining low driving voltage characteristics, as the optimized energy levels facilitate efficient charge recombination without requiring excessive voltage input.

Inventive Principle:
Principle #35Parameter changes

3Productivity

If polycyclic compound with specific structure is used to enhance triplet excitation energy level, then luminous efficiency is improved, but device complexity increases

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

Solution Approach 1:

The patent divides the complex polycyclic molecule into distinct functional segments: a central polycyclic aromatic core providing the high triplet energy level, and peripheral benzimidazole substituent groups providing electron transport and stability. This segmentation allows each component to be optimized independently while achieving the overall goal of high luminous efficiency, making the complexity manageable and designable.

Inventive Principle:
Principle #1Segmentation

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

This configuration results in high efficiency, long service life, and low voltage characteristics for the organic electroluminescence device, with the polycyclic compound acting as a host for blue phosphorescence or thermally activated delayed fluorescence, improving electron mobility and transport properties.

Implementation Method 1

development of a thermally activated delayed fluorescence (TADF) material which is capable of stably attaining these requirements

Methodology Applied
Scientific EffectThermally activated delayed fluorescence:

Implementation Method 2

the emission layer may have phosphorescence luminescence or thermally activated delayed fluorescence luminescence characteristics

Methodology Applied
Scientific EffectPhosphorescence: Phosphorescence

Implementation Method 3

improving electron mobility and transport properties

Methodology Applied
Scientific EffectElectron transport:

Implementation Method 4

holes and electrons injected from a first electrode and a second electrode recombine in an emission layer to generate an exciton, and the generated exciton returns (e.g., transitions) to a ground state and emits light

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Data Source

PatentUS12052915B2Organic electroluminescence device and polycyclic compound for organic electroluminescence device
Publication Date: 2024.07.30 SAMSUNG DISPLAY CO LTD
  • US12052915B2 patent drawing
  • US12052915B2 patent drawing
  • US12052915B2 patent drawing

AI summary

An organic electroluminescence device according to an embodiment of the present disclosure includes a first electrode, a second electrode facing the first electrode, and a plurality of organic layers between the first electrode and the second electrode, wherein at least one organic layer of the plurality of organic layers includes a polycyclic compound containing two aromatic 6-membered rings which are linked by a single bond, and a plurality of benzimidazole groups which are substituted at the two aromatic 6-membered rings, wherein each of the two aromatic 6-membered rings includes a carbon atom or a nitrogen atom as an atom for forming a ring.