Fluorene Polymer for White OLED Light Emission

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Solution Overview

Problem

Current polymers used in optoelectronic devices, such as OLEDs, face limitations in achieving optimal performance due to the lack of polymers with specific structural units that combine effective hole transport and light emissive properties, particularly in multi-layered white OLEDs requiring multiple light emissive layers.

Innovation Solution

Development of polymers with specific structural units, including fluorene derivatives and phenylpyridine-based ligands, synthesized through Suzuki cross-coupling reactions, which integrate both hole transport and light emissive moieties, enabling their use in multiple light emissive layers of white OLEDs.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If polymers with both hole transport and light emissive moieties are developed, then device performance is improved, but manufacturing complexity increases

Engineering Contradiction:
Improvedevice performanceVSAvoidpolymer structure complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent combines hole transport and light emissive functions into a single polymer molecule by integrating triarylamine-based hole transport moieties with fluorene-based light emissive moieties. This merging of functions into one material eliminates the need for separate layers, simplifying device structure while maintaining dual functionality for improved performance

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The developed polymer serves multiple functions simultaneously: it acts as both a hole transport material and a light emissive material. This multi-functionality allows a single polymer to replace what would traditionally require multiple separate materials and layers, resolving the contradiction between performance improvement and manufacturing complexity

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

2Ease of manufacture

If polymers are made insoluble to facilitate multi-layer device fabrication, then ease of manufacture is improved, but processing flexibility deteriorates

Engineering Contradiction:
Improvemulti-layer device fabricationVSAvoidprocessing flexibility
Core Design Contradiction:
Ease of manufactureVSAdaptability or versatility

Solution Approach 1:

The patent modifies the polymer's solubility parameters by incorporating specific side chains and molecular weight control during synthesis. The polymers are designed to be insoluble in common solvents used in multi-layer fabrication, which prevents unwanted mixing between layers during device assembly. This parameter change in solubility enables precise multi-layer fabrication while the insolvency itself becomes a controllable parameter for achieving desired processing characteristics

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 polymers exhibit a highest occupied molecular orbital (HOMO) of 4.8 eV, allowing for efficient light emission and are insoluble in solvents, facilitating their use in multi-layer optoelectronic devices, enhancing the performance and stability of white OLEDs.

Implementation Method 1

Optoelectronic devices, e.g. Organic Light Emitting Devices (OLEDs), which make use of thin film materials that emit light when subjected to a voltage bias

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Data Source

PatentEP2499181B1Polymer for optoelectronic device
Publication Date: 2020.05.13 BOE TECHNOLOGY GROUP CO LTD
  • EP2499181B1 patent drawing
  • EP2499181B1 patent drawing
  • EP2499181B1 patent drawing

AI summary

A polymer useful in an optoelectronic device comprises structural unit of formula I: wherein R1 is, independently at each occurrence, a C1-C20 aliphatic radical, a C3-C20 aromatic radical, or a C3-C20 cyclo aliphatic radical; a is, independently at each occurrence, an integer ranging from 0-4; Ar1 is aryl or heteroaryl; Ar2 is fluorene; R2 is alkylene, substituted alkylene, oxaalkylene, CO, or CO2; R3, R4 and R5 are independently hydrogen, alkyl, alkoxy, alkylaryl, aryl, arylalkyl, heteroaryl, substituted alkyl; substituted alkoxy, substituted alkylaryl, substituted aryl, substituted arylalkyl, or substituted heteroaryl; and L is derived from phenylpyridine, tolylpyridine, benzothienylpyridine, phenylisoquinoline, dibenzoquinozaline, fluorenylpyridine, ketopyrrole, 2-(1- naphthyl)benzoxazole)), 2-phenylbenzoxazole, 2 phenylbenzothiazole, coumarin, thienylpyridine, phenylpyridine, benzothienylpyridine, 3 methoxy-2-phenylpyridine, thienylpyridine, phenylimine, vinylpyridine, pyridylnaphthalene, pyridylpyrrole, pyridylimidazole, phenylindole, derivatives thereof or combinations thereof.