OLED Functional Layer Material for Hole Transport and Exciton Blocking

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Solution Overview

Problem

Existing organic materials in OLED light-emitting devices struggle to meet the increasing demands for efficiency, power consumption, and service life requirements.

Innovation Solution

A functional layer material is introduced, comprising specific structures represented by general formulas (I) to (IV), which includes triarylamine-based materials with fused ring aryl groups, heteroatoms, and various substituents to enhance hole transport and block electrons, improving emission efficiency and reducing voltage.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If existing organic materials are used in OLED light-emitting devices, then the device structure is simple and manufacturing is easier, but the luminous efficiency is insufficient, power consumption is high, and service life is limited

Engineering Contradiction:
Improveluminous efficiencyVSAvoidpower consumption
Core Design Contradiction:
ProductivityVSLoss of energy

Solution Approach 1:

The patent modifies the chemical structure parameters of organic materials by introducing specific functional groups (triazole, tetrazole, oxadiazole, etc.) and substituent patterns to optimize charge transport properties and energy levels, thereby improving luminous efficiency while reducing power consumption

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent develops composite organic material systems combining electron-transporting units, hole-transporting units, and exciton-blocking units in specific architectural configurations (formulas I-IV), creating materials with synergistic properties that simultaneously enhance efficiency and reduce energy loss

Inventive Principle:
Principle #40Composite materials

2Productivity

If existing organic materials are used in OLED light-emitting devices, then the material selection is simple, but the emission efficiency is insufficient and service life is limited

Engineering Contradiction:
Improveemission efficiencyVSAvoidservice life
Core Design Contradiction:
ProductivityVSDuration of action of stationary object

Solution Approach 1:

The patent introduces specialized functional units with localized properties: electron-transporting units (formula I) positioned to facilitate electron injection, hole-transporting units (formula II) for hole injection, and exciton-blocking units (formula III) to confine excitons in the light-emitting layer, each optimized for its specific function to enhance emission efficiency and device stability

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent designs materials with pre-optimized energy level alignments and charge transport pathways that facilitate efficient charge injection and exciton confinement from the outset, preventing energy loss and degradation mechanisms before they occur, thereby extending service life

Inventive Principle:
Principle #10Preliminary action

3Productivity

If functional layer material with complex structure (formulas I-IV) is used, then hole transport and electron blocking are enhanced, but device complexity increases

Engineering Contradiction:
Improvehole transport efficiencyVSAvoidmaterial structure complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent divides the functional layer material into distinct modular units: electron-transporting units (formula I), hole-transporting units (formula II), and exciton-blocking units (formula III), each with specific functions. These modules can be independently designed and combined in various configurations to achieve desired performance while maintaining manageable complexity

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent designs functional units that can serve multiple purposes: the triarylamine core structure provides both hole transport capability and structural stability, while substituent groups can be adjusted to simultaneously optimize energy levels, charge mobility, and exciton blocking properties, reducing the need for separate specialized components

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

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 functional layer material enhances hole transport, increases recombination probability, and blocks excitons, resulting in higher luminous efficiency, lower driving voltage, and extended service life of OLED devices.

Implementation Method 1

these electrons and holes are combined to form electron-hole pairs, and the formed electron-hole pairs are converted from a singlet state to a ground state to emit light

Methodology Applied
Scientific EffectHole transport: Conduction (electrical)

Implementation Method 2

A material of the first type of functional layer includes the functional layer material as described in any of the above embodiments... improves emission efficiency

Methodology Applied
Scientific EffectElectron blocking: Electrical Resistance

Implementation Method 3

The functional layer material enhances hole transport, increases recombination probability, and blocks excitons, resulting in higher luminous efficiency

Methodology Applied
Scientific EffectExciton blocking:

Implementation Method 4

these electrons and holes are combined to form electron-hole pairs, and the formed electron-hole pairs are converted from a singlet state to a ground state to emit light

Methodology Applied
Scientific EffectElectroluminescence: Electroluminescence

Data Source

PatentUS20260026257A1Functional Layer Material, Light-Emitting Device, and Display Panel
Publication Date: 2026.01.22 BOE TECHNOLOGY GROUP CO LTD
  • US20260026257A1 patent drawing
  • US20260026257A1 patent drawing
  • US20260026257A1 patent drawing

AI summary

A functional layer material is selected from any one of structures shown in a general formula (I). IA represents a first substitution unit including at least one fused ring aryl group; X is selected from any one of O, S and Se; Y is selected from any one of O, S, N(R4), C(R5R6) and a single bond; L1 is selected from any one of a single bond, substituted or unsubstituted C6 to C30 arylene groups, substituted or unsubstituted C1 to C30 heteroarylene groups, substituted or unsubstituted C7 to C30 aralkylene groups, and substituted or unsubstituted C2 to C30 heteroaralkylene groups; L2 is selected from any one of substituted or unsubstituted C6 to C30 arylene groups, substituted or unsubstituted C1 to C30 heteroarylene groups, substituted or unsubstituted C7 to C30 aralkylene groups, and substituted or unsubstituted C2 to C30 heteroaralkylene groups.