Abstract
Organic light-emitting diodes (OLEDs) exhibiting thermally activated delayed fluorescence (TADF) have attracted great interest because of their excellent exciton harvesting ability in electroluminescence (EL). While TADF-OLEDs show a high EL efficiency, the device operational stability is not necessarily satisfactory for commercial applications. Herein, the isotope effect of the host material on the device operational stability in TADF-OLEDs is investigated. It is unveiled that the deuterated host, i.e., PYD2Cz-d16, forms a denser film than that of the nondeuterated host, PYD2Cz, demonstrating enhanced stable amorphous nature and balanced carrier transport properties. In green TADF-OLEDs, the PYD2Cz-d16-based OLED considerably lengthens the device operational stability of LT95 (95% of the initial luminance) to ≈140 h at an initial luminance of 1000 cd m−2, which is 1.7 times longer than that of PYD2Cz. Device stabilities of blue TADF-OLEDs with PYD2Cz-d16 as a host are also demonstrated with an enhancement of 2 times in LT50 at an initial luminance of 1000 cd m−2. It is suggested that the deuterated materials have a positive effect on the device stability in not only TADF-OLEDs, but also all other OLEDs having fluorescence and phosphorescence emitters. © 2021 The Authors. Small Science published by Wiley-VCH GmbH.
Original language | English |
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Article number | 2000057 |
Journal | Small Science |
Volume | 1 |
Issue number | 4 |
Online published | 7 Feb 2021 |
DOIs | |
Publication status | Published - Apr 2021 |
Externally published | Yes |
Research Keywords
- deuteration of organic functional materials
- isotope effects
- operational stability
- organic light-emitting diodes
- thermally activated delayed fluorescence
Publisher's Copyright Statement
- This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/