Polycyclic Compound for Blue TADF OLED Emission

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Solution Overview

Problem

Current organic electroluminescence devices face challenges in achieving high emission efficiency, particularly in blue light emission, due to the difficulty in designing thermally activated delayed fluorescence (TADF) materials with small singlet-triplet energy gaps and efficient blue color emission.

Innovation Solution

A polycyclic compound with a specific structure, represented by Formula 1, is used in the emission layer of an organic electroluminescence device, featuring a carbonyl-containing dicyclic ring and amines as electron donors, which enables efficient blue light emission through TADF by minimizing the singlet-triplet energy difference and optimizing the combination of electron acceptors and donors.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If conventional TADF materials are used for blue light emission, then emission efficiency can be improved, but the singlet-triplet energy gap is too large to achieve efficient TADF

Engineering Contradiction:
Improveemission efficiencyVSAvoidsinglet-triplet energy gap
Core Design Contradiction:
ProductivityVSUse of energy by moving object

Solution Approach 1:

The patent changes the energy level parameters of the TADF material by designing a specific molecular structure with carbonyl-containing dicyclic ring as electron acceptor and amine as electron donor. This structural modification adjusts the HOMO-LUMO energy gap and singlet-triplet energy difference to achieve efficient TADF for blue light emission with wavelength of 470 nm or less.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite molecular structure combining electron acceptor (carbonyl-containing dicyclic ring) and electron donor (amine) groups within a single TADF material molecule. This composite structure enables simultaneous achievement of small singlet-triplet energy gap and blue color emission, resolving the contradiction between emission efficiency and energy gap.

Inventive Principle:
Principle #40Composite materials

2Productivity

If TADF materials with small singlet-triplet energy gap are designed, then emission efficiency improves, but achieving deep blue color emission (wavelength ≤470 nm) becomes difficult

Engineering Contradiction:
Improveemission efficiencyVSAvoidemission wavelength
Core Design Contradiction:
ProductivityVSIllumination intensity

Solution Approach 1:

The patent simultaneously optimizes multiple energy parameters including HOMO level, LUMO level, and singlet-triplet energy difference by adjusting the molecular structure. The specific combination of carbonyl-containing dicyclic ring and amine groups creates the right balance between small energy gap (for efficient TADF) and high energy emission (for deep blue color with wavelength ≤470 nm).

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 polycyclic compound achieves high external quantum efficiency and deep blue light emission with a maximum wavelength of 470 nm or less, overcoming the limitations of existing TADF materials in blue color emission.

Implementation Method 1

the difficulty in designing thermally activated delayed fluorescence (TADF) materials with small singlet-triplet energy gaps and efficient blue color emission

Methodology Applied
Scientific EffectThermally activated delayed fluorescence (TADF): Phosphorescence

Data Source

PatentUS10714693B2Polycyclic compound and organic electroluminescence device including the same
Publication Date: 2020.07.14 SAMSUNG DISPLAY CO LTD
  • US10714693B2 patent drawing
  • US10714693B2 patent drawing
  • US10714693B2 patent drawing

AI summary

A polycyclic compound and an organic electroluminescence device including the same. The polycyclic compound according to an example embodiment is represented by the following Formula 1.wherein in Formula 1, Cy1 is carbonyl-containing five- or six-membered and substituted or unsubstituted cyclic hydrocarbon or substituted or unsubstituted heterocycle, and R1 to R4 are each independently a hydrogen atom or a group represented by the following Formula 2 or 3.