Issue 20, 2022

Thermally activated delayed fluorescence poly(dendrimer)s – detrapping excitons for reverse intersystem crossing

Abstract

We report thermally activated delayed fluorescence (TADF) poly(dendrimer)s, composed of a norbornenyl-derived polymer backbone and dendritic side-chain chromophores comprising benzonitrile as the electron acceptor and two differently substituted first-generation 3,6-disubstituted carbazoles as electron donors. In particular, we compare the effect of the donor strength on the properties of the poly(dendrimer)s and their dendrimer analogues. The groups attached to the carbazolyl moieties to form the donor units were either 9,9-di-n-propylfluorene or diphenylamine. All four compounds were found to have TADF emission with neat film photoluminescence quantum yields (PLQYs) of up to 27%. The di-n-propylfluorenyl groups were found to afford a higher degree of protection from intrapolymer interchromophore interactions along the poly(dendrimer) backbone, and the solution and neat film PLQYs were similar. Photoluminescence studies performed at 77 K revealed that the triplet excitons can migrate along the poly(dendrimer) chain until they reach a chromophore that has the configuration required for charge transfer emission. Also, neat films of the poly(dendrimer)s were found to transport holes and electrons with reasonably balanced mobilities, whilst the dendrimers only had measurable hole mobilities. Organic light-emitting diodes with neat and blended emissive layers were found to have modest performance.

Graphical abstract: Thermally activated delayed fluorescence poly(dendrimer)s – detrapping excitons for reverse intersystem crossing

Supplementary files

Article information

Article type
Paper
Submitted
26 okt 2021
Accepted
03 mai 2022
First published
13 mai 2022

J. Mater. Chem. C, 2022,10, 8109-8124

Thermally activated delayed fluorescence poly(dendrimer)s – detrapping excitons for reverse intersystem crossing

E. V. Puttock, C. S. K. Ranasinghe, M. Babazadeh, J. C. M. Kistemaker, J. Jang, M. Gao, D. M. Huang, C. Adachi, P. L. Burn and P. E. Shaw, J. Mater. Chem. C, 2022, 10, 8109 DOI: 10.1039/D1TC05151B

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