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A flexible plasma-treated silver-nanowire electrode for organic light-emitting devices

Silver nanowires (AgNWs) are a promising candidate to replace indium tin oxide (ITO) as transparent electrode material. However, the loose contact at the junction of the AgNWs and residual surfactant polyvinylpyrrolidone (PVP) increase the sheet resistance of the AgNWs. In this paper, an argon (Ar)...

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Detalles Bibliográficos
Autores principales: Li, Jun, Tao, Ye, Chen, Shufen, Li, Huiying, Chen, Ping, Wei, Meng-zhu, Wang, Hu, Li, Kun, Mazzeo, Marco, Duan, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705724/
https://www.ncbi.nlm.nih.gov/pubmed/29184113
http://dx.doi.org/10.1038/s41598-017-16721-7
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author Li, Jun
Tao, Ye
Chen, Shufen
Li, Huiying
Chen, Ping
Wei, Meng-zhu
Wang, Hu
Li, Kun
Mazzeo, Marco
Duan, Yu
author_facet Li, Jun
Tao, Ye
Chen, Shufen
Li, Huiying
Chen, Ping
Wei, Meng-zhu
Wang, Hu
Li, Kun
Mazzeo, Marco
Duan, Yu
author_sort Li, Jun
collection PubMed
description Silver nanowires (AgNWs) are a promising candidate to replace indium tin oxide (ITO) as transparent electrode material. However, the loose contact at the junction of the AgNWs and residual surfactant polyvinylpyrrolidone (PVP) increase the sheet resistance of the AgNWs. In this paper, an argon (Ar) plasma treatment method is applied to pristine AgNWs to remove the PVP layer and enhance the contact between AgNWs. By adjusting the processing time, we obtained AgNWs with a sheet resistance of 7.2Ω/□ and a transmittance of 78% at 550 nm. To reduce the surface roughness of the AgNWs, a peel-off process was used to transfer the AgNWs to a flexible NOA63 substrate. Then, an OLED was fabricated with the plasma-treated AgNWs electrode as anode. The highest brightness (27000 cd/m(2)) and current efficiency (11.8 cd/A) was achieved with a 30 nm thick light emitting layer of tris-(8-hydroxyquinoline) aluminum doped with 1% 10-(2-benzothiazolyl)-2,3,6,7-tetrahydro-1,1,7,7-tetramethyl-1H,5 H,11H-(1)-benzopyropyrano(6,7-8-I,j)quinolizin-11-one. Compared to thermal annealing, the plasma-treated AgNW film has a lower sheet resistance, a shorter processing time, and a better hole-injection. Our results indicate that plasma treatment is an effective and efficient method to enhance the conductivity of AgNW films, and the plasma-treated AgNW electrode is suitable to manufacture flexible organic optoelectronic devices.
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spelling pubmed-57057242017-12-05 A flexible plasma-treated silver-nanowire electrode for organic light-emitting devices Li, Jun Tao, Ye Chen, Shufen Li, Huiying Chen, Ping Wei, Meng-zhu Wang, Hu Li, Kun Mazzeo, Marco Duan, Yu Sci Rep Article Silver nanowires (AgNWs) are a promising candidate to replace indium tin oxide (ITO) as transparent electrode material. However, the loose contact at the junction of the AgNWs and residual surfactant polyvinylpyrrolidone (PVP) increase the sheet resistance of the AgNWs. In this paper, an argon (Ar) plasma treatment method is applied to pristine AgNWs to remove the PVP layer and enhance the contact between AgNWs. By adjusting the processing time, we obtained AgNWs with a sheet resistance of 7.2Ω/□ and a transmittance of 78% at 550 nm. To reduce the surface roughness of the AgNWs, a peel-off process was used to transfer the AgNWs to a flexible NOA63 substrate. Then, an OLED was fabricated with the plasma-treated AgNWs electrode as anode. The highest brightness (27000 cd/m(2)) and current efficiency (11.8 cd/A) was achieved with a 30 nm thick light emitting layer of tris-(8-hydroxyquinoline) aluminum doped with 1% 10-(2-benzothiazolyl)-2,3,6,7-tetrahydro-1,1,7,7-tetramethyl-1H,5 H,11H-(1)-benzopyropyrano(6,7-8-I,j)quinolizin-11-one. Compared to thermal annealing, the plasma-treated AgNW film has a lower sheet resistance, a shorter processing time, and a better hole-injection. Our results indicate that plasma treatment is an effective and efficient method to enhance the conductivity of AgNW films, and the plasma-treated AgNW electrode is suitable to manufacture flexible organic optoelectronic devices. Nature Publishing Group UK 2017-11-28 /pmc/articles/PMC5705724/ /pubmed/29184113 http://dx.doi.org/10.1038/s41598-017-16721-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Jun
Tao, Ye
Chen, Shufen
Li, Huiying
Chen, Ping
Wei, Meng-zhu
Wang, Hu
Li, Kun
Mazzeo, Marco
Duan, Yu
A flexible plasma-treated silver-nanowire electrode for organic light-emitting devices
title A flexible plasma-treated silver-nanowire electrode for organic light-emitting devices
title_full A flexible plasma-treated silver-nanowire electrode for organic light-emitting devices
title_fullStr A flexible plasma-treated silver-nanowire electrode for organic light-emitting devices
title_full_unstemmed A flexible plasma-treated silver-nanowire electrode for organic light-emitting devices
title_short A flexible plasma-treated silver-nanowire electrode for organic light-emitting devices
title_sort flexible plasma-treated silver-nanowire electrode for organic light-emitting devices
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5705724/
https://www.ncbi.nlm.nih.gov/pubmed/29184113
http://dx.doi.org/10.1038/s41598-017-16721-7
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