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Persistent Dimer Emission in Thermally Activated Delayed Fluorescence Materials
[Image: see text] We expose significant changes in the emission color of carbazole-based thermally activated delayed fluorescence (TADF) emitters that arise from the presence of persistent dimer states in thin films and organic light-emitting diodes (OLEDs). Direct photoexcitation of this dimer stat...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501699/ https://www.ncbi.nlm.nih.gov/pubmed/31080540 http://dx.doi.org/10.1021/acs.jpcc.9b01458 |
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author | Etherington, Marc K. Kukhta, Nadzeya A. Higginbotham, Heather F. Danos, Andrew Bismillah, Aisha N. Graves, David R. McGonigal, Paul R. Haase, Nils Morherr, Antonia Batsanov, Andrei S. Pflumm, Christof Bhalla, Vandana Bryce, Martin R. Monkman, Andrew P. |
author_facet | Etherington, Marc K. Kukhta, Nadzeya A. Higginbotham, Heather F. Danos, Andrew Bismillah, Aisha N. Graves, David R. McGonigal, Paul R. Haase, Nils Morherr, Antonia Batsanov, Andrei S. Pflumm, Christof Bhalla, Vandana Bryce, Martin R. Monkman, Andrew P. |
author_sort | Etherington, Marc K. |
collection | PubMed |
description | [Image: see text] We expose significant changes in the emission color of carbazole-based thermally activated delayed fluorescence (TADF) emitters that arise from the presence of persistent dimer states in thin films and organic light-emitting diodes (OLEDs). Direct photoexcitation of this dimer state in 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) reveals the significant influence of dimer species on the color purity of its photoluminescence and electroluminescence. The dimer species is sensitive to the sample preparation method, and its enduring presence contributes to the widely reported concentration-mediated red shift in the photoluminescence and electroluminescence of evaporated thin films. This discovery has implications on the usability of these, and similar, molecules for OLEDs and explains disparate electroluminescence spectra presented in the literature for these compounds. The dimerization-controlled changes observed in the TADF process and photoluminescence efficiency mean that careful consideration of dimer states is imperative in the design of future TADF emitters and the interpretation of previously reported studies of carbazole-based TADF materials. |
format | Online Article Text |
id | pubmed-6501699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-65016992019-05-08 Persistent Dimer Emission in Thermally Activated Delayed Fluorescence Materials Etherington, Marc K. Kukhta, Nadzeya A. Higginbotham, Heather F. Danos, Andrew Bismillah, Aisha N. Graves, David R. McGonigal, Paul R. Haase, Nils Morherr, Antonia Batsanov, Andrei S. Pflumm, Christof Bhalla, Vandana Bryce, Martin R. Monkman, Andrew P. J Phys Chem C Nanomater Interfaces [Image: see text] We expose significant changes in the emission color of carbazole-based thermally activated delayed fluorescence (TADF) emitters that arise from the presence of persistent dimer states in thin films and organic light-emitting diodes (OLEDs). Direct photoexcitation of this dimer state in 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) reveals the significant influence of dimer species on the color purity of its photoluminescence and electroluminescence. The dimer species is sensitive to the sample preparation method, and its enduring presence contributes to the widely reported concentration-mediated red shift in the photoluminescence and electroluminescence of evaporated thin films. This discovery has implications on the usability of these, and similar, molecules for OLEDs and explains disparate electroluminescence spectra presented in the literature for these compounds. The dimerization-controlled changes observed in the TADF process and photoluminescence efficiency mean that careful consideration of dimer states is imperative in the design of future TADF emitters and the interpretation of previously reported studies of carbazole-based TADF materials. American Chemical Society 2019-04-03 2019-05-02 /pmc/articles/PMC6501699/ /pubmed/31080540 http://dx.doi.org/10.1021/acs.jpcc.9b01458 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Etherington, Marc K. Kukhta, Nadzeya A. Higginbotham, Heather F. Danos, Andrew Bismillah, Aisha N. Graves, David R. McGonigal, Paul R. Haase, Nils Morherr, Antonia Batsanov, Andrei S. Pflumm, Christof Bhalla, Vandana Bryce, Martin R. Monkman, Andrew P. Persistent Dimer Emission in Thermally Activated Delayed Fluorescence Materials |
title | Persistent Dimer Emission in Thermally Activated Delayed
Fluorescence Materials |
title_full | Persistent Dimer Emission in Thermally Activated Delayed
Fluorescence Materials |
title_fullStr | Persistent Dimer Emission in Thermally Activated Delayed
Fluorescence Materials |
title_full_unstemmed | Persistent Dimer Emission in Thermally Activated Delayed
Fluorescence Materials |
title_short | Persistent Dimer Emission in Thermally Activated Delayed
Fluorescence Materials |
title_sort | persistent dimer emission in thermally activated delayed
fluorescence materials |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501699/ https://www.ncbi.nlm.nih.gov/pubmed/31080540 http://dx.doi.org/10.1021/acs.jpcc.9b01458 |
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