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Ornamenting of Blue Thermally Activated Delayed Fluorescence Emitters by Anchor Groups for the Minimization of Solid-State Solvation and Conformation Disorder Corollaries in Non-Doped and Doped Organic Light-Emitting Diodes

[Image: see text] Motivated to minimize the effects of solid-state solvation and conformation disorder on emission properties of donor–acceptor-type emitters, we developed five new asymmetric multiple donor–acceptor type derivatives of tert-butyl carbazole and trifluoromethyl benzene exploiting diff...

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Autores principales: Mahmoudi, Malek, Gudeika, Dalius, Kutsiy, Stepan, Simokaitiene, Jurate, Butkute, Rita, Skhirtladze, Levani, Woon, Kai Lin, Volyniuk, Dmytro, Grazulevicius, Juozas Vidas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9460442/
https://www.ncbi.nlm.nih.gov/pubmed/36000983
http://dx.doi.org/10.1021/acsami.2c12475
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author Mahmoudi, Malek
Gudeika, Dalius
Kutsiy, Stepan
Simokaitiene, Jurate
Butkute, Rita
Skhirtladze, Levani
Woon, Kai Lin
Volyniuk, Dmytro
Grazulevicius, Juozas Vidas
author_facet Mahmoudi, Malek
Gudeika, Dalius
Kutsiy, Stepan
Simokaitiene, Jurate
Butkute, Rita
Skhirtladze, Levani
Woon, Kai Lin
Volyniuk, Dmytro
Grazulevicius, Juozas Vidas
author_sort Mahmoudi, Malek
collection PubMed
description [Image: see text] Motivated to minimize the effects of solid-state solvation and conformation disorder on emission properties of donor–acceptor-type emitters, we developed five new asymmetric multiple donor–acceptor type derivatives of tert-butyl carbazole and trifluoromethyl benzene exploiting different electron-accepting anchoring groups. Using this design strategy, for a compound containing four di-tert-butyl carbazole units as donors as well as 5-methyl pyrimidine and trifluoromethyl acceptor moieties, small singlet-triplet splitting of ca. 0.03 eV, reverse intersystem crossing rate of 1 × 10(6) s(–1), and high photoluminescence quantum yield of neat film of ca. 75% were achieved. This compound was also characterized by the high value of hole and electron mobilities of 8.9 × 10(–4) and 5.8 × 10(–4) cm(2) V(–1) s(–1) at an electric field of 4.7 × 10(5) V/cm, showing relatively good hole/electron balance, respectively. Due to the lowest conformational disorder and solid-state solvation effects, this compound demonstrated very similar emission properties (emission colors) in non-doped and differently doped organic light-emitting diodes (OLEDs). The lowest conformational disorder was observed for the compound with the additional accepting moiety inducing steric hindrance, limiting donor–acceptor dihedral rotational freedom. It can be exploited in the multi-donor–acceptor approach, increasing the efficiency. Using an emitter exhibiting the minimized solid-state solvation and conformation disorder effects, the sky blue OLED with the emitting layer of this compound dispersed in host 1,3-bis(N-carbazolyl)benzene displayed an emission peak at 477 nm, high brightness over 39 000 cd/m(2), and external quantum efficiency up to 15.9% along with a maximum current efficiency of 42.6 cd/A and a maximum power efficiency of 24.1 lm/W.
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spelling pubmed-94604422022-09-10 Ornamenting of Blue Thermally Activated Delayed Fluorescence Emitters by Anchor Groups for the Minimization of Solid-State Solvation and Conformation Disorder Corollaries in Non-Doped and Doped Organic Light-Emitting Diodes Mahmoudi, Malek Gudeika, Dalius Kutsiy, Stepan Simokaitiene, Jurate Butkute, Rita Skhirtladze, Levani Woon, Kai Lin Volyniuk, Dmytro Grazulevicius, Juozas Vidas ACS Appl Mater Interfaces [Image: see text] Motivated to minimize the effects of solid-state solvation and conformation disorder on emission properties of donor–acceptor-type emitters, we developed five new asymmetric multiple donor–acceptor type derivatives of tert-butyl carbazole and trifluoromethyl benzene exploiting different electron-accepting anchoring groups. Using this design strategy, for a compound containing four di-tert-butyl carbazole units as donors as well as 5-methyl pyrimidine and trifluoromethyl acceptor moieties, small singlet-triplet splitting of ca. 0.03 eV, reverse intersystem crossing rate of 1 × 10(6) s(–1), and high photoluminescence quantum yield of neat film of ca. 75% were achieved. This compound was also characterized by the high value of hole and electron mobilities of 8.9 × 10(–4) and 5.8 × 10(–4) cm(2) V(–1) s(–1) at an electric field of 4.7 × 10(5) V/cm, showing relatively good hole/electron balance, respectively. Due to the lowest conformational disorder and solid-state solvation effects, this compound demonstrated very similar emission properties (emission colors) in non-doped and differently doped organic light-emitting diodes (OLEDs). The lowest conformational disorder was observed for the compound with the additional accepting moiety inducing steric hindrance, limiting donor–acceptor dihedral rotational freedom. It can be exploited in the multi-donor–acceptor approach, increasing the efficiency. Using an emitter exhibiting the minimized solid-state solvation and conformation disorder effects, the sky blue OLED with the emitting layer of this compound dispersed in host 1,3-bis(N-carbazolyl)benzene displayed an emission peak at 477 nm, high brightness over 39 000 cd/m(2), and external quantum efficiency up to 15.9% along with a maximum current efficiency of 42.6 cd/A and a maximum power efficiency of 24.1 lm/W. American Chemical Society 2022-08-24 2022-09-07 /pmc/articles/PMC9460442/ /pubmed/36000983 http://dx.doi.org/10.1021/acsami.2c12475 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Mahmoudi, Malek
Gudeika, Dalius
Kutsiy, Stepan
Simokaitiene, Jurate
Butkute, Rita
Skhirtladze, Levani
Woon, Kai Lin
Volyniuk, Dmytro
Grazulevicius, Juozas Vidas
Ornamenting of Blue Thermally Activated Delayed Fluorescence Emitters by Anchor Groups for the Minimization of Solid-State Solvation and Conformation Disorder Corollaries in Non-Doped and Doped Organic Light-Emitting Diodes
title Ornamenting of Blue Thermally Activated Delayed Fluorescence Emitters by Anchor Groups for the Minimization of Solid-State Solvation and Conformation Disorder Corollaries in Non-Doped and Doped Organic Light-Emitting Diodes
title_full Ornamenting of Blue Thermally Activated Delayed Fluorescence Emitters by Anchor Groups for the Minimization of Solid-State Solvation and Conformation Disorder Corollaries in Non-Doped and Doped Organic Light-Emitting Diodes
title_fullStr Ornamenting of Blue Thermally Activated Delayed Fluorescence Emitters by Anchor Groups for the Minimization of Solid-State Solvation and Conformation Disorder Corollaries in Non-Doped and Doped Organic Light-Emitting Diodes
title_full_unstemmed Ornamenting of Blue Thermally Activated Delayed Fluorescence Emitters by Anchor Groups for the Minimization of Solid-State Solvation and Conformation Disorder Corollaries in Non-Doped and Doped Organic Light-Emitting Diodes
title_short Ornamenting of Blue Thermally Activated Delayed Fluorescence Emitters by Anchor Groups for the Minimization of Solid-State Solvation and Conformation Disorder Corollaries in Non-Doped and Doped Organic Light-Emitting Diodes
title_sort ornamenting of blue thermally activated delayed fluorescence emitters by anchor groups for the minimization of solid-state solvation and conformation disorder corollaries in non-doped and doped organic light-emitting diodes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9460442/
https://www.ncbi.nlm.nih.gov/pubmed/36000983
http://dx.doi.org/10.1021/acsami.2c12475
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