TADF OLED Emitters With Small ΔEST for Rare-Metal-Free Efficiency
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Solution Overview
Problem
Existing organic light-emitting elements rely on phosphorescent materials containing rare and expensive metals, and there is a need for a more efficient and cost-effective alternative that can harness both singlet and triplet excitons to achieve high electroluminescent efficiency.
Innovation Solution
The use of benzobisoxazole, benzobisthiazole, and benzobisimidazole compounds with a small energy gap between S1 and T1 states to enable thermally activated delayed fluorescence (TADF), allowing for up-conversion of triplet excitons to singlet excitons, thereby enhancing exciton formation efficiency.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Productivity
If phosphorescent materials containing rare metals (Ir or Pt) are used, then electroluminescent efficiency is improved by harvesting triplet excitons, but cost increases and resource sustainability deteriorates
Solution Approach 1:
The patent extracts and eliminates the rare metal components (Ir, Pt) from the phosphorescent material system by developing a purely organic TADF emitter that achieves comparable or superior electroluminescent efficiency through a different mechanism (reverse intersystem crossing) that does not require heavy metals
Solution Approach 2:
The patent changes the fundamental parameter of exciton harvesting mechanism from phosphorescence (requiring triplet state emission with heavy metal assistance) to thermally activated delayed fluorescence (utilizing reverse intersystem crossing from triplet to singlet state), thereby achieving high efficiency without rare metals
2Device complexity
If conventional fluorescent materials are used, then material simplicity is maintained, but electroluminescent efficiency deteriorates due to utilization of only 25% of excitons
Solution Approach 1:
The patent changes the energy gap parameter (ΔEST between S1 and T1 states) to be sufficiently small, enabling thermally activated reverse intersystem crossing from triplet to singlet state, thereby allowing fluorescent materials to harvest both singlet and triplet excitons for a maximum of 100% internal quantum efficiency
Solution Approach 2:
The patent introduces dynamic thermal activation that enables the system to overcome the energy gap between S1 and T1 states at operating temperatures, allowing bidirectional intersystem crossing and enabling the fluorescent emitter to utilize both singlet and triplet excitons dynamically
3Productivity
If phosphorescent materials are used to harvest triplet excitons, then electroluminescent efficiency is improved, but device complexity and manufacturing cost increase
Solution Approach 1:
The patent replaces expensive, resource-limited phosphorescent materials containing rare metals with inexpensive, readily available organic compounds that can be synthesized through standard organic chemistry processes, thereby dramatically reducing manufacturing cost and complexity
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 compounds achieve external quantum efficiencies of over 5% and reduced efficiency roll-off at high luminance, providing a cost-effective and efficient alternative to traditional phosphorescent materials.
Implementation Method 1
thermally activated delayed fluorescence (TADF) emitters and/or hosts of formula (I), which have a sufficiently small energy gap between S1 and T1 (ΔEST) to enable up-conversion of the triplet exciton from T1 to S1
Implementation Method 2
thermally activated delayed fluorescence (TADF) as a third generation luminescent material
Data Source
AI summary
The present invention relates to organic light emitting elements, comprising thermally activated delayed fluorescence (TADF) emitters and/or hosts of formulawhich have a sufficiently small energy gap between S1 and T1 (ΔEST) to enable up-conversion of the triplet exciton from T1 to S1. The organic light emitting elements show high electroluminescent efficiency.


