Ionic Multi-Resonant Thermally Activated Delayed Fluorescence Emitters for Light Emitting Electrochemical Cells

24 June 2022, Version 3
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

We designed and synthesized two new ionic thermally activated delayed fluorescent (TADF) emitters that are charged analogues of a known multiresonant TADF (MR-TADF) compound, DiKTa. The emission of the charged derivatives is red-shifted compared to the parent com-pound. For instance, DiKTa-OBuIm emits in the green (λPL = 499 nm, 1 wt% in mCP) while DiKTa-DPA-OBuIm emits in the red (λPL = 577 nm, 1 wt% in mCP). In 1 wt% mCP films, both emitters showed good photoluminescence quantum yields of 71% and 61%, and delayed life-times of 316.6 μs and 241.7 μs, respectively, for DiKTa-OBuIm and DiKTa-DPA-OBuIm, leading to reverse intersystem crossing rates of 2.85 × 103 s-1 and 3.04 × 103 s-1. Light-emitting electrochemical cells were prepared using both DiKTa-OBuIm and DiKTa-DPA-OBuIm as ac-tive emitters showing green (λmax = 534 nm) and red (λmax = 656 nm) emission, respectively.

Keywords

multi-resonant thermally activated delayed fluorescence
MR-TADF
light-emitting electrochemical cells
LECs
LEECs

Supplementary materials

Title
Description
Actions
Title
ESI
Description
Electronic Supporting Information
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.