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Copper(II) meso-Tetraphenyl- and meso-Tetrafluorenyl Porphyrinates as Charge Carrier Transporting and Electroluminescent Compounds
[Image: see text] Studies on copper(II) tetrafluorenyl porphyrinate (CuTFP) and copper(II) tetraphenyl porphyrinate (CuTPP) have been focused on the charge carrier transport in their solid films and electroluminescence of their composites. In the dye layers deposited by resistive thermal evaporation...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928336/ https://www.ncbi.nlm.nih.gov/pubmed/35309452 http://dx.doi.org/10.1021/acsomega.1c06557 |
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author | Chernyadyev, Andrey Yu. Aleksandrov, Alexey E. Lypenko, Dmitry A. Tyurin, Vladimir S. Tameev, Alexey R. Tsivadze, Aslan Yu. |
author_facet | Chernyadyev, Andrey Yu. Aleksandrov, Alexey E. Lypenko, Dmitry A. Tyurin, Vladimir S. Tameev, Alexey R. Tsivadze, Aslan Yu. |
author_sort | Chernyadyev, Andrey Yu. |
collection | PubMed |
description | [Image: see text] Studies on copper(II) tetrafluorenyl porphyrinate (CuTFP) and copper(II) tetraphenyl porphyrinate (CuTPP) have been focused on the charge carrier transport in their solid films and electroluminescence of their composites. In the dye layers deposited by resistive thermal evaporation, the mobilities of holes and electrons are on the order of 10(–5) and 10(–6) cm(2) V(–1) s(–1) for the charge transport under the influence of traps, and the charge mobility reaches the order of 10(–3) cm(2) V(–1) s(–1) at space-charge-limited current in the nontrapping mode. For the dye molecules, the correlation between the mobility of charge carriers and the distribution of the electron density on the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO), which serve as hopping sites for holes and electrons, respectively, is considered. Organic light-emitting diodes incorporating the dye molecules as emitting dopants demonstrate electroluminescence in the near-infrared (IR) range. |
format | Online Article Text |
id | pubmed-8928336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-89283362022-03-18 Copper(II) meso-Tetraphenyl- and meso-Tetrafluorenyl Porphyrinates as Charge Carrier Transporting and Electroluminescent Compounds Chernyadyev, Andrey Yu. Aleksandrov, Alexey E. Lypenko, Dmitry A. Tyurin, Vladimir S. Tameev, Alexey R. Tsivadze, Aslan Yu. ACS Omega [Image: see text] Studies on copper(II) tetrafluorenyl porphyrinate (CuTFP) and copper(II) tetraphenyl porphyrinate (CuTPP) have been focused on the charge carrier transport in their solid films and electroluminescence of their composites. In the dye layers deposited by resistive thermal evaporation, the mobilities of holes and electrons are on the order of 10(–5) and 10(–6) cm(2) V(–1) s(–1) for the charge transport under the influence of traps, and the charge mobility reaches the order of 10(–3) cm(2) V(–1) s(–1) at space-charge-limited current in the nontrapping mode. For the dye molecules, the correlation between the mobility of charge carriers and the distribution of the electron density on the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO), which serve as hopping sites for holes and electrons, respectively, is considered. Organic light-emitting diodes incorporating the dye molecules as emitting dopants demonstrate electroluminescence in the near-infrared (IR) range. American Chemical Society 2022-03-01 /pmc/articles/PMC8928336/ /pubmed/35309452 http://dx.doi.org/10.1021/acsomega.1c06557 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Chernyadyev, Andrey Yu. Aleksandrov, Alexey E. Lypenko, Dmitry A. Tyurin, Vladimir S. Tameev, Alexey R. Tsivadze, Aslan Yu. Copper(II) meso-Tetraphenyl- and meso-Tetrafluorenyl Porphyrinates as Charge Carrier Transporting and Electroluminescent Compounds |
title | Copper(II) meso-Tetraphenyl- and meso-Tetrafluorenyl Porphyrinates as Charge Carrier Transporting
and Electroluminescent Compounds |
title_full | Copper(II) meso-Tetraphenyl- and meso-Tetrafluorenyl Porphyrinates as Charge Carrier Transporting
and Electroluminescent Compounds |
title_fullStr | Copper(II) meso-Tetraphenyl- and meso-Tetrafluorenyl Porphyrinates as Charge Carrier Transporting
and Electroluminescent Compounds |
title_full_unstemmed | Copper(II) meso-Tetraphenyl- and meso-Tetrafluorenyl Porphyrinates as Charge Carrier Transporting
and Electroluminescent Compounds |
title_short | Copper(II) meso-Tetraphenyl- and meso-Tetrafluorenyl Porphyrinates as Charge Carrier Transporting
and Electroluminescent Compounds |
title_sort | copper(ii) meso-tetraphenyl- and meso-tetrafluorenyl porphyrinates as charge carrier transporting
and electroluminescent compounds |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8928336/ https://www.ncbi.nlm.nih.gov/pubmed/35309452 http://dx.doi.org/10.1021/acsomega.1c06557 |
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