Heteroleptic Iridium Complexes for Saturated OLED 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 efficiently emit light with improved performance and flexibility.

Innovation Solution

The development of a compound with the Formula Ir(LA)m(LB)3-m, where moiety B is a polycyclic fused ring structure, ring C is a 5- or 6-membered aromatic ring, and moieties D and E are monocyclic or polycyclic fused rings, used in the organic layer of OLEDs to enhance light emission properties.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Illumination intensity

If conventional organic materials are used in OLEDs, then the devices can be fabricated with flexibility and cost advantages, but the emission color saturation and efficiency are insufficient for full-color displays

Engineering Contradiction:
Improveemission color saturationVSAvoidfabrication complexity
Core Design Contradiction:
Illumination intensityVSEase of manufacture

Solution Approach 1:

The patent modifies the molecular structure of organic emitters by incorporating specific heterocyclic rings (triazole, tetrazole, oxadiazole, thiadiazole) and adjusting substituent groups to optimize HOMO-LUMO energy gaps. This changes the optical parameters of the materials to achieve saturated red, green, and blue emissions while maintaining compatibility with conventional OLED fabrication processes

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention creates composite organic emitter molecules combining multiple functional units: heterocyclic core structures, aromatic substituents (phenyl, naphthyl, anthryl groups), and electron-donating or withdrawing groups. These composite molecular structures enable simultaneous achievement of color saturation and fabrication ease

Inventive Principle:
Principle #40Composite materials

2Illumination intensity

If white OLED with absorption filters is used to produce saturated colors, then color display is achieved, but the emission efficiency and device performance are reduced

Engineering Contradiction:
Improvecolor saturationVSAvoidemission efficiency
Core Design Contradiction:
Illumination intensityVSLoss of energy

Solution Approach 1:

The patent extracts and eliminates the need for absorption filters by directly engineering organic emitter molecules to emit saturated red, green, and blue light. This removes the energy-wasting filtering step while achieving the desired color output, thereby improving emission efficiency

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

By changing the molecular parameters of the organic emitters through heterocyclic ring incorporation and substituent modification, the patent enables direct emission of saturated colors without requiring post-emission filtering, thus eliminating energy loss in the filtering process

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 improves the emission efficiency and color saturation of OLEDs, leading to better performance in terms of electroluminescence and flexibility, enabling the production of high-quality, full-color displays.

Implementation Method 1

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

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Data Source

PatentUS20220384743A1Organic electroluminescent materials and devices
Publication Date: 2022.12.01 UNIVERSAL DISPLAY CORP
  • US20220384743A1 patent drawing
  • US20220384743A1 patent drawing
  • US20220384743A1 patent drawing

AI summary

Heteroleptic compounds having a Formula Ir(LA)m(LB)3-m, having the structure of Formula Ior Formula II,are described. In Formula I and Formula II, moiety B is a polycyclic fused ring structure comprising at least four rings; ring C is a 5- or 6-membered aromatic ring; moieties D and E are independently a monocyclic or polycyclic fused ring structure; Z1 and Z2 are each independently C or N; each RA, RB, RC, RD, and RE is hydrogen or a General Substituent; and when ring C is a phenyl ring, RC collectively comprises two or more C atoms. Formulations, OLEDs, and consumer products incorporating the compounds are also described.