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Photoactivated Refractive Index Anisotropy in Fluorescent Thiophene Derivatives

[Image: see text] The optical control of anisotropy in materials is highly advantageous for many technological applications, including the real-time modulation of another light signal in photonic switches and sensors. Here, we introduce three thiophene derivatives with a donor–acceptor structure, wh...

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Autores principales: Szukalski, Adam, Haupa, Karolina A., Adamow, Alina, Cheret, Yohan, Hue, Raphael, El-Ghayoury, Abdelkrim, Sahraoui, Bouchta, Pisignano, Dario, Mysliwiec, Jaroslaw, Camposeo, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7706105/
https://www.ncbi.nlm.nih.gov/pubmed/33282054
http://dx.doi.org/10.1021/acs.jpcc.0c07455
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author Szukalski, Adam
Haupa, Karolina A.
Adamow, Alina
Cheret, Yohan
Hue, Raphael
El-Ghayoury, Abdelkrim
Sahraoui, Bouchta
Pisignano, Dario
Mysliwiec, Jaroslaw
Camposeo, Andrea
author_facet Szukalski, Adam
Haupa, Karolina A.
Adamow, Alina
Cheret, Yohan
Hue, Raphael
El-Ghayoury, Abdelkrim
Sahraoui, Bouchta
Pisignano, Dario
Mysliwiec, Jaroslaw
Camposeo, Andrea
author_sort Szukalski, Adam
collection PubMed
description [Image: see text] The optical control of anisotropy in materials is highly advantageous for many technological applications, including the real-time modulation of another light signal in photonic switches and sensors. Here, we introduce three thiophene derivatives with a donor–acceptor structure, which feature different positions of an electron-acceptor nitrile group, and both photoalignment and luminescence properties. Quantum chemical calculations highlight the presence of trans-forms stable at room temperature and metastable cis-isomers. Besides photoluminescence peaked at 440–460 nm and 0.4 ns lifetime, the three nonlinear optical chromophores exhibit photoinduced anisotropy of the refractive index closely depending on the specific molecular structure, with higher values of birefringence at lower driving signal being obtained for ortho substitution of the nitrile group. All-optical modulation of an external light beam at rates of hundreds of hertz is demonstrated in the fluorescent systems. This finding opens an interesting route to multispectral photonic switches embedded in the active layers of light-emitting devices.
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spelling pubmed-77061052020-12-02 Photoactivated Refractive Index Anisotropy in Fluorescent Thiophene Derivatives Szukalski, Adam Haupa, Karolina A. Adamow, Alina Cheret, Yohan Hue, Raphael El-Ghayoury, Abdelkrim Sahraoui, Bouchta Pisignano, Dario Mysliwiec, Jaroslaw Camposeo, Andrea J Phys Chem C Nanomater Interfaces [Image: see text] The optical control of anisotropy in materials is highly advantageous for many technological applications, including the real-time modulation of another light signal in photonic switches and sensors. Here, we introduce three thiophene derivatives with a donor–acceptor structure, which feature different positions of an electron-acceptor nitrile group, and both photoalignment and luminescence properties. Quantum chemical calculations highlight the presence of trans-forms stable at room temperature and metastable cis-isomers. Besides photoluminescence peaked at 440–460 nm and 0.4 ns lifetime, the three nonlinear optical chromophores exhibit photoinduced anisotropy of the refractive index closely depending on the specific molecular structure, with higher values of birefringence at lower driving signal being obtained for ortho substitution of the nitrile group. All-optical modulation of an external light beam at rates of hundreds of hertz is demonstrated in the fluorescent systems. This finding opens an interesting route to multispectral photonic switches embedded in the active layers of light-emitting devices. American Chemical Society 2020-11-09 2020-11-19 /pmc/articles/PMC7706105/ /pubmed/33282054 http://dx.doi.org/10.1021/acs.jpcc.0c07455 Text en © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Szukalski, Adam
Haupa, Karolina A.
Adamow, Alina
Cheret, Yohan
Hue, Raphael
El-Ghayoury, Abdelkrim
Sahraoui, Bouchta
Pisignano, Dario
Mysliwiec, Jaroslaw
Camposeo, Andrea
Photoactivated Refractive Index Anisotropy in Fluorescent Thiophene Derivatives
title Photoactivated Refractive Index Anisotropy in Fluorescent Thiophene Derivatives
title_full Photoactivated Refractive Index Anisotropy in Fluorescent Thiophene Derivatives
title_fullStr Photoactivated Refractive Index Anisotropy in Fluorescent Thiophene Derivatives
title_full_unstemmed Photoactivated Refractive Index Anisotropy in Fluorescent Thiophene Derivatives
title_short Photoactivated Refractive Index Anisotropy in Fluorescent Thiophene Derivatives
title_sort photoactivated refractive index anisotropy in fluorescent thiophene derivatives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7706105/
https://www.ncbi.nlm.nih.gov/pubmed/33282054
http://dx.doi.org/10.1021/acs.jpcc.0c07455
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