Fluorinated Carbazole Host Materials for Blue OLED Efficiency

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Solution Overview

Problem

Existing organic electroluminescent devices face challenges in reducing power consumption and improving efficiency, particularly due to non-radiative deactivation in blue phosphorescent devices using mCP as a host material, which has a high T1 level and large ionization potential, leading to increased voltage requirements.

Innovation Solution

Incorporating specific compounds represented by formulas [1] to [3] in the organic electroluminescent device, which act as host materials or light-emitting materials in the light-emitting layer, with a high T1 level and lower ionization potential, to reduce non-radiative deactivation and lower driving voltage, along with a metal complex-based electron transport layer to enhance efficiency.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If mCP is used as the host material in blue phosphorescent devices, then the device structure is simple and easy to manufacture, but non-radiative deactivation occurs due to high T1 level (66 kcal/mol) matching with pure blue phosphorescent materials (T1 > 65 kcal/mol), reducing efficiency

Engineering Contradiction:
Improveease of manufactureVSAvoidnon-radiative deactivation
Core Design Contradiction:
Ease of manufactureVSLoss of energy

Solution Approach 1:

The patent modifies the host material's T1 energy level parameter by introducing fluorine atoms at specific positions (2,6-positions of pyridine rings) in the carbazole derivative structure. This parameter change raises the host material's T1 level above 70 kcal/mol, creating an energy gap that prevents non-radiative deactivation with phosphorescent materials having T1 > 65 kcal/mol, while maintaining the simple molecular structure for ease of manufacture

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite host material system by combining fluorinated carbazole derivatives with specific phosphorescent emitters (Ir(ppy)3, Ir(piq)3, or PtOEP). This composite approach ensures energy transfer from host to emitter while preventing energy back-transfer that would cause non-radiative deactivation, resolving the efficiency problem while maintaining manufacturing simplicity

Inventive Principle:
Principle #40Composite materials

2Ease of manufacture

If mCP is used as the host material, then the device structure is simple, but the large ionization potential (6.0 eV) requires high device driving voltage, increasing power consumption

Engineering Contradiction:
Improveease of manufactureVSAvoidpower consumption
Core Design Contradiction:
Ease of manufactureVSUse of energy by moving object

Solution Approach 1:

The patent changes the ionization potential parameter of the host material by fluorine substitution at the 2,6-positions of carbazole units. This structural modification lowers the ionization potential from mCP's 6.0 eV to below 5.8 eV, reducing the energy barrier for hole injection and transport, thereby decreasing the device driving voltage and power consumption while preserving the molecular simplicity for easy manufacture

Inventive Principle:
Principle #35Parameter changes

3Illumination intensity

If pure blue phosphorescent materials with T1 level in excess of 65 kcal/mol are used, then the emission color is pure blue, but non-radiative deactivation occurs when combined with mCP host material, reducing quantum efficiency

Engineering Contradiction:
Improveblue color purityVSAvoidnon-radiative deactivation
Core Design Contradiction:
Illumination intensityVSLoss of energy

Solution Approach 1:

The patent raises the host material's T1 energy level parameter above 70 kcal/mol through fluorine substitution, creating an upward energy gradient relative to the phosphorescent emitter's T1 level (>65 kcal/mol). This parameter change prevents energy back-transfer from emitter to host that would cause non-radiative deactivation, allowing pure blue emission to be maintained with high quantum efficiency

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The fluorinated carbazole derivative acts as an energy transfer intermediary between electrical excitation and the phosphorescent emitter. The modified host material efficiently transfers energy to the emitter while its elevated T1 level serves as an energy barrier that prevents harmful back-transfer, mediating the energy flow to eliminate non-radiative deactivation pathways

Inventive Principle:
Principle #24Intermediary (Mediator)

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 use of these compounds results in improved external and internal quantum efficiencies, reduced power consumption, and prolonged device life with enhanced blue color purity and emission characteristics.

Implementation Method 1

an organic electroluminescent device which can emit light by converting electric energy into light

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Implementation Method 2

The external quantum efficiency of the phosphorescent device described therein is greatly enhanced

Methodology Applied
Scientific EffectPhosphorescence: Phosphorescence

Data Source

PatentUS7740959B2Organic electroluminescent device
Publication Date: 2010.06.22 UDC IRELAND
  • US7740959B2 patent drawing
  • US7740959B2 patent drawing
  • US7740959B2 patent drawing

AI summary

An organic electroluminescent device comprises: a pair of electrodes; and at least one organic layer comprising a light-emitting layer, said at least one organic layer being between the electrodes, wherein at least one of said at least one organic layer comprises at least one kind of compound represented by formula [1]:wherein Q101 represents a linking group, the bond between the carbon atom bonded by R107 and the carbon atom bonded by R108 may be a single bond or a double bond (provided that when the bond between the carbon atom bonded by R107 and the carbon atom bonded by R108 is a double bond, R106 and R109 are not present), R102 to R105 each represents a substituent, R106 to R109 each represents a hydrogen atom or a substituent, R107 and R108 may combine to form a condensed ring, and n101 represents an integer of 1 or more].