Polycyclic Aromatic Compound for Deep Blue OLED Emission

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Solution Overview

Problem

Current organic electroluminescent elements face challenges in achieving high energy efficiency and deep blue light emission with high color purity due to limitations in exciton utilization efficiency and broad emission spectra, particularly with conventional fluorescent and phosphorescent materials.

Innovation Solution

A novel polycyclic aromatic compound is developed, featuring a structure with linked aromatic rings and specific substituents, which serves as a light-emitting material in organic electroluminescent elements, enhancing emission efficiency and color purity by utilizing thermally assisted delayed fluorescence mechanisms.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Device complexity

If conventional fluorescent materials are used, then the device structure is simple, but the exciton utilization efficiency is low (about 25%)

Engineering Contradiction:
Improvedevice structureVSAvoidexciton utilization efficiency
Core Design Contradiction:
Device complexityVSUse of energy by moving object

Solution Approach 1:

The patent introduces a heavy atom (Ir or Pt) as an intermediary in the light-emitting compound structure. This heavy atom mediates the spin-state transitions, enabling efficient triplet exciton utilization through phosphorescence while maintaining a relatively simple device structure. The heavy atom effect facilitates intersystem crossing and enables high exciton utilization efficiency without complex device architecture modifications.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Use of energy by moving object

If phosphorescent materials are used, then the exciton utilization efficiency reaches 100%, but the color purity is low due to broad emission spectrum

Engineering Contradiction:
Improveexciton utilization efficiencyVSAvoidcolor purity
Core Design Contradiction:
Use of energy by moving objectVSManufacturing precision

Solution Approach 1:

The patent employs local quality by using a rigid polycyclic aromatic ligand structure (such as triphenylene or pyrene derivatives) with specific substitution patterns. This localized rigid structure confines the electron cloud and reduces vibrational relaxation, resulting in narrow emission bands. The ligand's specific molecular geometry and electron distribution create localized emission zones with high color purity while maintaining phosphorescent efficiency.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent uses composite materials by combining phosphorescent metal centers (Ir or Pt) with organic polycyclic aromatic ligands. This composite structure integrates the high exciton utilization of phosphorescence with the narrow emission characteristics of rigid aromatic systems. The synergistic combination achieves both 100% exciton utilization and high color purity through the coordinated effects of the metal center and organic ligand framework.

Inventive Principle:
Principle #40Composite materials

3Use of energy by moving object

If TADF compounds are used, then the exciton utilization reaches 100%, but the emission spectrum is broad with low color purity

Engineering Contradiction:
Improveexciton utilizationVSAvoidcolor purity
Core Design Contradiction:
Use of energy by moving objectVSManufacturing precision

Solution Approach 1:

The patent converts the typically harmful non-radiative triplet decay in fluorescent systems into a beneficial mechanism by introducing heavy atoms that enable phosphorescence. The heavy atom effect transforms the harmful triplet state (which would otherwise decay non-radiatively) into a useful phosphorescent emission pathway, achieving high exciton utilization while maintaining narrow emission bands through the rigid ligand structure.

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

4Adaptability or versatility

If conventional light-emitting materials are used, then the material selection is broad, but the deep blue light emission with high color purity cannot be achieved

Engineering Contradiction:
Improvematerial selection rangeVSAvoiddeep blue emission quality
Core Design Contradiction:
Adaptability or versatilityVSManufacturing precision

Solution Approach 1:

The patent achieves deep blue emission with high color purity by precisely controlling molecular parameters: using polycyclic aromatic hydrocarbons with specific ring numbers (4-6 fused rings), optimizing the HOMO-LUMO energy gap through substituent effects, and adjusting the molecular planarity. These parameter changes in the molecular structure directly control the emission wavelength and bandwidth, enabling deep blue light with narrow emission spectra.

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 achieves high emission efficiency and narrow emission peak widths, enabling organic devices to produce deep blue light with high color purity, improving the performance of organic electroluminescent elements.

Implementation Method 1

which serves as a light-emitting material in organic electroluminescent elements, enhancing emission efficiency and color purity by utilizing thermally assisted delayed fluorescence mechanisms

Methodology Applied
Scientific EffectThermally assisted delayed fluorescence:

Implementation Method 2

an organic electroluminescent element (organic EL element) using an organic material

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Data Source

PatentUS11877506B2Polycyclic aromatic compound
Publication Date: 2024.01.16 SK MATERIALS JNC CO LTD
  • US11877506B2 patent drawing
  • US11877506B2 patent drawing
  • US11877506B2 patent drawing

AI summary

A polycyclic aromatic compound represented by Formula (1) is provided by the invention:wherein A11 ring, A21 ring, A31 ring, B11 ring, B21 ring, C11 ring, and C31 ring are an aryl or heteroaryl ring which may be substituted, Y11, Y21, Y31 are B or the like, X11, X12, X21, X22, X31, X32 are >O or >N—R, R in the above >N—R is an and which may be substituted or the like, R in the above >N—R or the like may be bonded to A11 ring, A21 ring, A31 ring, B11 ring, B21 ring, C11 ring, and/or C31 ring by a linking group or a single bond; and at least one hydrogen in the compound represented by Formula (1) may be replaced with deuterium, cyano, or a halogen.