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Interplay between Long-Range Crystal Order and Short-Range Molecular Interactions Tunes Carrier Mobility in Liquid Crystal Dyes

[Image: see text] We investigated the influence of molecular packing on the optical and electrical properties of the liquid crystalline dye 4,7-bis[5-(2-fluoro-4-pentyl-phenyl)-2-thienyl]-2,1,3-benzothiadiazole (FPPTB). FPPTB is crystalline at room temperature, exhibits a nematic phase at temperatur...

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Autores principales: Tchamba Yimga, Nadine, Ramanan, Charusheela, Borchert, Holger, Parisi, Jürgen, Untenecker, Harald, Kirsch, Peer, von Hauff, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330658/
https://www.ncbi.nlm.nih.gov/pubmed/28139915
http://dx.doi.org/10.1021/acsami.6b14715
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author Tchamba Yimga, Nadine
Ramanan, Charusheela
Borchert, Holger
Parisi, Jürgen
Untenecker, Harald
Kirsch, Peer
von Hauff, Elizabeth
author_facet Tchamba Yimga, Nadine
Ramanan, Charusheela
Borchert, Holger
Parisi, Jürgen
Untenecker, Harald
Kirsch, Peer
von Hauff, Elizabeth
author_sort Tchamba Yimga, Nadine
collection PubMed
description [Image: see text] We investigated the influence of molecular packing on the optical and electrical properties of the liquid crystalline dye 4,7-bis[5-(2-fluoro-4-pentyl-phenyl)-2-thienyl]-2,1,3-benzothiadiazole (FPPTB). FPPTB is crystalline at room temperature, exhibits a nematic phase at temperatures above 149 °C and is in an isotropic melt at temperatures above 230 °C. Solution processed FPPTB films were subject to thermal annealing through these phase transition temperatures and characterized with X-ray diffraction and polarized optical microscopy. Cooling FPPTB films from the nematic and isotropic phases increased crystal domain size, but also induced local structural variations in the molecular packing of crystalline FPPTB. The decrease in long-range order was correlated with an increase in short-range π–π interactions, leading to changes in molecular aggregation which persisted even when the FPPTB films were cooled to room temperature. Annealing-induced changes in molecular aggregation were confirmed with optical spectroscopy. The carrier mobility in FPPTB films increased over 2 orders of magnitude from (2.2 ± 0.4) × 10(–5) cm(2) V(–1) s(–1) in as-spun films to μ = (5.0 ± 0.8) × 10(–3) cm(2) V(–1) s(–1) in films cooled from the isotropic melt. We discuss the relationship between thermal stability and high carrier mobility values in terms of the interplay between long-range molecular order and increased π–π interactions between molecular pairs in the FPPTB film.
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spelling pubmed-53306582017-03-02 Interplay between Long-Range Crystal Order and Short-Range Molecular Interactions Tunes Carrier Mobility in Liquid Crystal Dyes Tchamba Yimga, Nadine Ramanan, Charusheela Borchert, Holger Parisi, Jürgen Untenecker, Harald Kirsch, Peer von Hauff, Elizabeth ACS Appl Mater Interfaces [Image: see text] We investigated the influence of molecular packing on the optical and electrical properties of the liquid crystalline dye 4,7-bis[5-(2-fluoro-4-pentyl-phenyl)-2-thienyl]-2,1,3-benzothiadiazole (FPPTB). FPPTB is crystalline at room temperature, exhibits a nematic phase at temperatures above 149 °C and is in an isotropic melt at temperatures above 230 °C. Solution processed FPPTB films were subject to thermal annealing through these phase transition temperatures and characterized with X-ray diffraction and polarized optical microscopy. Cooling FPPTB films from the nematic and isotropic phases increased crystal domain size, but also induced local structural variations in the molecular packing of crystalline FPPTB. The decrease in long-range order was correlated with an increase in short-range π–π interactions, leading to changes in molecular aggregation which persisted even when the FPPTB films were cooled to room temperature. Annealing-induced changes in molecular aggregation were confirmed with optical spectroscopy. The carrier mobility in FPPTB films increased over 2 orders of magnitude from (2.2 ± 0.4) × 10(–5) cm(2) V(–1) s(–1) in as-spun films to μ = (5.0 ± 0.8) × 10(–3) cm(2) V(–1) s(–1) in films cooled from the isotropic melt. We discuss the relationship between thermal stability and high carrier mobility values in terms of the interplay between long-range molecular order and increased π–π interactions between molecular pairs in the FPPTB film. American Chemical Society 2017-01-31 2017-02-22 /pmc/articles/PMC5330658/ /pubmed/28139915 http://dx.doi.org/10.1021/acsami.6b14715 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Tchamba Yimga, Nadine
Ramanan, Charusheela
Borchert, Holger
Parisi, Jürgen
Untenecker, Harald
Kirsch, Peer
von Hauff, Elizabeth
Interplay between Long-Range Crystal Order and Short-Range Molecular Interactions Tunes Carrier Mobility in Liquid Crystal Dyes
title Interplay between Long-Range Crystal Order and Short-Range Molecular Interactions Tunes Carrier Mobility in Liquid Crystal Dyes
title_full Interplay between Long-Range Crystal Order and Short-Range Molecular Interactions Tunes Carrier Mobility in Liquid Crystal Dyes
title_fullStr Interplay between Long-Range Crystal Order and Short-Range Molecular Interactions Tunes Carrier Mobility in Liquid Crystal Dyes
title_full_unstemmed Interplay between Long-Range Crystal Order and Short-Range Molecular Interactions Tunes Carrier Mobility in Liquid Crystal Dyes
title_short Interplay between Long-Range Crystal Order and Short-Range Molecular Interactions Tunes Carrier Mobility in Liquid Crystal Dyes
title_sort interplay between long-range crystal order and short-range molecular interactions tunes carrier mobility in liquid crystal dyes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5330658/
https://www.ncbi.nlm.nih.gov/pubmed/28139915
http://dx.doi.org/10.1021/acsami.6b14715
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