Carbazolyl Host Material for Blue OLED Triplet Energy Confinement

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Organic electroluminescent devices face challenges in achieving high luminous efficiency and driving stability due to limitations in host materials, including insufficient triplet energy, imbalance in electrical charge injection/transport characteristics, and durability issues, particularly with carbazole-based compounds.

Innovation Solution

A compound with carbazolyl groups linked to a six-membered aromatic ring at the ortho position is developed, suitable for use in organic electroluminescent devices as a host material, enhancing triplet energy and charge balance, and incorporated into the light-emitting layer with a phosphorescent dopant to improve luminous efficiency and stability.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Loss of energy

If CBP is used as a host material for green phosphorescent emitters, then luminous characteristics are relatively good, but triplet energy is insufficient for blue phosphorescent emitters causing energy transfer loss

Engineering Contradiction:
Improvetriplet energy transfer lossVSAvoidluminous efficiency
Core Design Contradiction:
Loss of energyVSReliability

Solution Approach 1:

The patent modifies the host material structure by introducing carbazolyl groups linked to six-membered aromatic rings at ortho positions, which increases the triplet energy level parameter. This structural parameter change enables the host material to confine triplet energy of blue phosphorescent emitters effectively, preventing energy transfer loss while maintaining good luminous characteristics.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent employs composite host materials combining carbazole units with six-membered aromatic rings (such as phenyl, pyridyl groups) to create a new material system. This composite structure achieves both high triplet energy for blue emitter confinement and balanced charge injection/transport properties, resolving the contradiction between energy retention and luminous efficiency.

Inventive Principle:
Principle #40Composite materials

2Reliability

If host material triplet energy is increased to confine phosphorescent emitter energy, then luminous efficiency is enhanced, but durability deteriorates

Engineering Contradiction:
Improveluminous efficiencyVSAvoiddevice durability
Core Design Contradiction:
ReliabilityVSDuration of action of stationary object

Solution Approach 1:

The patent introduces electron-transporting groups (such as pyridyl groups) at specific positions (ortho positions) of the carbazole-based host material structure. This local structural modification creates regions with enhanced electron transport capability that stabilize the material under operational stress, improving durability without compromising the overall high triplet energy and luminous efficiency.

Inventive Principle:
Principle #3Local quality

3Reliability

If electron transport property is enhanced in host material, then charge balance improves, but manufacturing complexity increases

Engineering Contradiction:
Improvecharge balanceVSAvoidmaterial synthesis complexity
Core Design Contradiction:
ReliabilityVSEase of manufacture

Solution Approach 1:

The carbazole-based host material structure serves multiple functions simultaneously: it provides high triplet energy for blue emitter confinement, enables balanced charge injection and transport through integrated electron-transporting groups, and maintains structural stability. This multi-functionality in a single molecular framework simplifies device fabrication compared to using multiple separate materials layers.

Inventive Principle:
Principle #6Universality (Multi-functionality)

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 achieves high luminous efficiency, balanced electrical charge recombination, and improved durability, leading to enhanced performance in organic electroluminescent devices with increased driving stability and practical usability in display applications.

Implementation Method 1

as the lowest triplet energy of the compound is sufficiently high to confine the lowest triplet energy of the dopant, the compound can effectively suppress the transfer of the triplet energy from the dopant to the host molecule

Methodology Applied
Scientific EffectTriplet energy confinement:

Implementation Method 2

Upon application of an electrical field between the electrodes, electrons are injected from the cathode and holes are injected from the anode and they recombine in the light-emitting layer with emission of light

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Implementation Method 3

The use of phosphorescence, that is, emission of light from the excited triplet state, is expected to enhance the luminous efficiency three to four times that of the conventional devices utilizing fluorescence

Methodology Applied
Scientific EffectPhosphorescence: Phosphorescence

Data Source

PatentUS8859109B2Compound for organic electroluminescent device and organic electroluminescent device using the same
Publication Date: 2014.10.14 NIPPON STEEL CHEM & MATERIAL CO LTD
  • US8859109B2 patent drawing
  • US8859109B2 patent drawing
  • US8859109B2 patent drawing

AI summary

Disclosed is an organic electroluminescent device (organic EL device) that is improved in luminous efficiency, fully secured of driving stability, and of simple structure. The organic EL device comprises a light-emitting layer between an anode and a cathode piled one upon another on a substrate and the light-emitting layer comprises a phosphorescent dopant and a compound containing carbazolyl groups at both ends represented by the following formula (1) as a host material. In formula (1), X is independently CH optionally containing a substituent or N and L is a direct bond, an ethylene group, or an acetylene group.