OLED Metal Complex Ligands for Saturated Color Emission

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Solution Overview

Problem

Current organic light-emitting diode (OLED) technologies face challenges in achieving saturated colors for full-color displays, particularly in red, green, and blue emissions, which are essential for industry standards, and there is a need for materials that can be efficiently processed in solution form for cost-effective and flexible device fabrication.

Innovation Solution

A compound with a specific bidentate ligand structure, coordinated to metals like Ir, Pt, or other transition metals, is used in an organic layer of OLEDs, forming a 5-membered chelate ring, which enhances the emission properties and allows for solution processability, enabling the production of OLEDs with improved color saturation and flexibility.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Illumination intensity

If conventional OLED materials are used to achieve saturated colors for full-color displays, then color saturation is improved, but manufacturing cost and fabrication complexity increase

Engineering Contradiction:
Improvecolor saturationVSAvoidfabrication cost
Core Design Contradiction:
Illumination intensityVSEase of manufacture

Solution Approach 1:

The patent modifies the molecular structure of organic emissive materials by changing chemical parameters (adding specific ligands like Formula I to metal centers such as Ir, Pt, Pd, Ru, Rh, Os, Re, Cu, Ag, or Au) to achieve saturated color emission. This allows the materials to meet industry color standards while maintaining solution processability, thereby reducing fabrication costs and complexity compared to conventional materials that require expensive vacuum deposition processes.

Inventive Principle:
Principle #35Parameter changes

2Illumination intensity

If conventional OLED materials are used for color display applications, then color emission is achieved, but solution processability and flexibility for fabrication are reduced

Engineering Contradiction:
Improvecolor emissionVSAvoidsolution processability
Core Design Contradiction:
Illumination intensityVSEase of operation

Solution Approach 1:

The patent changes the chemical parameters of OLED materials by incorporating specific ligand structures (Formula I) coordinated to metal centers, which enables both saturated color emission and solution processability. This dual capability allows the materials to be fabricated using low-cost solution-based methods such as spin-coating or inkjet printing on flexible substrates, while still achieving the required color emission performance for display applications.

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 use of this compound in OLEDs results in enhanced emission properties, enabling the production of OLEDs that meet industry color standards and offers the potential for flexible and cost-effective fabrication, suitable for various display applications.

Implementation Method 1

One application for phosphorescent emissive molecules is a full color display

Methodology Applied
Scientific EffectPhosphorescence: Phosphorescence

Implementation Method 2

OLEDs make use of thin organic films that emit light when voltage is applied across the device

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Data Source

PatentUS12122793B2Organic electroluminescent materials and devices
Publication Date: 2024.10.22 UNIVERSAL DISPLAY CORP
  • US12122793B2 patent drawing
  • US12122793B2 patent drawing
  • US12122793B2 patent drawing

AI summary

A compound comprising a first bidentate ligand LA, wherein LA comprises a structure of Formula I;wherein Z is selected from the group consisting of O, S, NR, BR, CRKRL, SiRKRL, —CRKRLCRMRN—, —SiRKRLSiRMRN—, —CRKRLO—, —SiRKRLO—, and —CRK═CRL—;wherein ring A, ring B, and ring C are each independently a 5-membered carbocyclic ring, 5-membered heterocyclic ring, 6-membered carbocyclic ring or 6-membered heterocyclic ring;wherein LA is coordinated to a metal M forming a 5-membered chelate ring;wherein M is selected from the group consisting of Ir, Pt, Pd, Ru, Rh, Os, Re, Cu, Ag, and Au;wherein RA, RB, and RC each represent mono to the maximum allowable substitution, or no substitution;wherein each R, RK, RL, RM, RN, RA, RB, and RC is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof;wherein M is optionally coordinated to one or more other ligands;wherein any two substituents are optionally joined or fused together to form a ring; andwith the provision that LA does not comprise the following structure: