Polycyclic Hetero-Aromatic Host for Blue Phosphorescent OLEDs

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Solution Overview

Problem

Phosphorescent organic electroluminescence (EL) devices face challenges in achieving high efficiency and low driving voltage due to the need for materials with excellent charge-injecting and charge-transporting properties, which often compromise charge balance and device lifetime.

Innovation Solution

A compound with two or more structures directly bonded by a single bond, featuring highly planar polycyclic hetero-aromatic rings, is used as a material for the emitting layer, maintaining high triplet energy and suitable for blue phosphorescent devices, allowing for efficient confinement of triplet energy and reduced driving voltage.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Power

If a material with excellent charge-injecting properties or charge-transporting properties is used, then the driving voltage is lowered, but charge balance in the emitting layer deteriorates, leading to shortened device lifetime

Engineering Contradiction:
Improvedriving voltageVSAvoiddevice lifetime
Core Design Contradiction:
PowerVSReliability

Solution Approach 1:

The patent modifies the chemical structure of the host material by introducing specific substituents (electron-donating or electron-withdrawing groups) to adjust charge transport properties. This allows optimization of both charge balance and device lifetime while maintaining acceptable driving voltage levels

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs composite host materials combining different molecular components with complementary properties. This enables simultaneous achievement of good charge balance, long device lifetime, and reduced driving voltage through synergistic effects of the composite system

Inventive Principle:
Principle #40Composite materials

2Loss of energy

If a host material with triplet energy larger than the phosphorescent dopant material is used, then triplet energy is efficiently confined in the emitting layer, but device complexity increases due to material selection constraints

Engineering Contradiction:
Improvetriplet energy confinement efficiencyVSAvoidmaterial selection complexity
Core Design Contradiction:
Loss of energyVSDevice complexity

Solution Approach 1:

The patent systematically adjusts the triplet energy parameter of host materials through structural modifications, creating a series of host compounds with progressively optimized energy levels. This reduces material selection complexity by providing a structured approach to matching host-dopant energy levels

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 compound enables a decrease in driving voltage and an increase in efficiency of organic EL devices while maintaining a long device lifetime by effectively confining triplet energy and optimizing charge balance.

Implementation Method 1

In order to efficiently confine the triplet energy of the phosphorescent dopant material in the emitting layer, it is required to use a host material having a triplet energy larger than the triplet energy of the phosphorescent dopant material in the emitting layer

Methodology Applied
Scientific EffectTriplet energy confinement:

Implementation Method 2

since phosphorescence emission utilizes triplet excitons, a compound used for forming an emitting layer is required to have a large energy gap

Methodology Applied
Scientific EffectPhosphorescence: Phosphorescence

Data Source

PatentUS10505123B2Compound and organic electroluminescent device using same
Publication Date: 2019.12.10 IDEMITSU KOSAN CO LTD
  • US10505123B2 patent drawing
  • US10505123B2 patent drawing
  • US10505123B2 patent drawing

AI summary

A compound that includes a structure including two or more structures represented by the following formula (1) in the same molecule and in which at least two of the structures represented by the formula (1) are directly bonded to each other by a single bond.