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Conjoint use of Naphthalene Diimide and Fullerene Derivatives to Generate Organic Semiconductors for n–type Organic Thin Film Transistors

In this paper, we described the design, synthesis, and characterization of two novel naphthalene diimide (NDI) core‐based targets modified with terminal fullerene (C(60)) yield – so called S4 and S5, in which NDI bearing 1 and 2 molecules of C(60), respectively. The absorption, electrochemical and t...

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Autores principales: Birajdar, Shailesh S., Brixi, Samantha, Rao, Pedada Srinivasa, Bhosale, Rajesh S., Kobaisi, Mohammad Al, Gupta, Akhil, Lessard, Benoît H., Bhosale, Sidhanath V., Bhosale, Sheshanath V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015730/
https://www.ncbi.nlm.nih.gov/pubmed/33543836
http://dx.doi.org/10.1002/open.202000230
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author Birajdar, Shailesh S.
Brixi, Samantha
Rao, Pedada Srinivasa
Bhosale, Rajesh S.
Kobaisi, Mohammad Al
Gupta, Akhil
Lessard, Benoît H.
Bhosale, Sidhanath V.
Bhosale, Sheshanath V.
author_facet Birajdar, Shailesh S.
Brixi, Samantha
Rao, Pedada Srinivasa
Bhosale, Rajesh S.
Kobaisi, Mohammad Al
Gupta, Akhil
Lessard, Benoît H.
Bhosale, Sidhanath V.
Bhosale, Sheshanath V.
author_sort Birajdar, Shailesh S.
collection PubMed
description In this paper, we described the design, synthesis, and characterization of two novel naphthalene diimide (NDI) core‐based targets modified with terminal fullerene (C(60)) yield – so called S4 and S5, in which NDI bearing 1 and 2 molecules of C(60), respectively. The absorption, electrochemical and thin‐film transistor characteristics of the newly developed targets were investigated in detail. Both S4 and S5 displayed broad absorption in the 450–500 nm region, owing to the effect of conjugation due to fullerene functionalities. The electrochemical measurement suggested that the HOMO and the LUMO energy levels can be altered with the number of C(60) units. Both S4 and S5 were employed as organic semiconductor materials in n‐channel transistors. The thin film transistor based on S4 exhibited superior electron mobility (μe) values ranging from 1.20×10(−4) to 3.58×10(−4) cm(2) V(−1) s(−1) with a current on‐off ratio varying from 10(2) to 10(3) in comparison with the performance of S5 based transistor, which exhibited μe ranging from 8.33×10(−5) to 2.03×10(−4) cm(2) V(−1) s(−1) depending on channel lengths.
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spelling pubmed-80157302021-04-02 Conjoint use of Naphthalene Diimide and Fullerene Derivatives to Generate Organic Semiconductors for n–type Organic Thin Film Transistors Birajdar, Shailesh S. Brixi, Samantha Rao, Pedada Srinivasa Bhosale, Rajesh S. Kobaisi, Mohammad Al Gupta, Akhil Lessard, Benoît H. Bhosale, Sidhanath V. Bhosale, Sheshanath V. ChemistryOpen Full Papers In this paper, we described the design, synthesis, and characterization of two novel naphthalene diimide (NDI) core‐based targets modified with terminal fullerene (C(60)) yield – so called S4 and S5, in which NDI bearing 1 and 2 molecules of C(60), respectively. The absorption, electrochemical and thin‐film transistor characteristics of the newly developed targets were investigated in detail. Both S4 and S5 displayed broad absorption in the 450–500 nm region, owing to the effect of conjugation due to fullerene functionalities. The electrochemical measurement suggested that the HOMO and the LUMO energy levels can be altered with the number of C(60) units. Both S4 and S5 were employed as organic semiconductor materials in n‐channel transistors. The thin film transistor based on S4 exhibited superior electron mobility (μe) values ranging from 1.20×10(−4) to 3.58×10(−4) cm(2) V(−1) s(−1) with a current on‐off ratio varying from 10(2) to 10(3) in comparison with the performance of S5 based transistor, which exhibited μe ranging from 8.33×10(−5) to 2.03×10(−4) cm(2) V(−1) s(−1) depending on channel lengths. John Wiley and Sons Inc. 2021-02-05 /pmc/articles/PMC8015730/ /pubmed/33543836 http://dx.doi.org/10.1002/open.202000230 Text en © 2021 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full Papers
Birajdar, Shailesh S.
Brixi, Samantha
Rao, Pedada Srinivasa
Bhosale, Rajesh S.
Kobaisi, Mohammad Al
Gupta, Akhil
Lessard, Benoît H.
Bhosale, Sidhanath V.
Bhosale, Sheshanath V.
Conjoint use of Naphthalene Diimide and Fullerene Derivatives to Generate Organic Semiconductors for n–type Organic Thin Film Transistors
title Conjoint use of Naphthalene Diimide and Fullerene Derivatives to Generate Organic Semiconductors for n–type Organic Thin Film Transistors
title_full Conjoint use of Naphthalene Diimide and Fullerene Derivatives to Generate Organic Semiconductors for n–type Organic Thin Film Transistors
title_fullStr Conjoint use of Naphthalene Diimide and Fullerene Derivatives to Generate Organic Semiconductors for n–type Organic Thin Film Transistors
title_full_unstemmed Conjoint use of Naphthalene Diimide and Fullerene Derivatives to Generate Organic Semiconductors for n–type Organic Thin Film Transistors
title_short Conjoint use of Naphthalene Diimide and Fullerene Derivatives to Generate Organic Semiconductors for n–type Organic Thin Film Transistors
title_sort conjoint use of naphthalene diimide and fullerene derivatives to generate organic semiconductors for n–type organic thin film transistors
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015730/
https://www.ncbi.nlm.nih.gov/pubmed/33543836
http://dx.doi.org/10.1002/open.202000230
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