Raman spectroscopic characterization of a thiophene-based active material for resistive organic nonvolatile memories

A combined theoretical and experimental Raman study is presented on a diphenyl bithiophene molecule known as a good candidate for the development of organic nonvolatile memory devices. Spectroscopic markers suitable to distinguish the different stable conformers of the molecule have been predicted a...

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Veröffentlicht in:Journal of Raman spectroscopy 2010-04, Vol.41 (4), p.406-413
Hauptverfasser: Fazzi, Daniele, Canesi, Eleonora Valeria, Bertarelli, Chiara, Castiglioni, Chiara, Negri, Fabrizia, Zerbi, Giuseppe
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container_issue 4
container_start_page 406
container_title Journal of Raman spectroscopy
container_volume 41
creator Fazzi, Daniele
Canesi, Eleonora Valeria
Bertarelli, Chiara
Castiglioni, Chiara
Negri, Fabrizia
Zerbi, Giuseppe
description A combined theoretical and experimental Raman study is presented on a diphenyl bithiophene molecule known as a good candidate for the development of organic nonvolatile memory devices. Spectroscopic markers suitable to distinguish the different stable conformers of the molecule have been predicted and detected. The combined analysis of theoretical and experimental Raman spectra recorded in solution indicates that at room temperature a dynamical equilibrium, characterized by interconversion between the two more stable conformers (namely trans and cis), takes place and that the more populated species is the cis form. Referring to the solid phase instead, Raman spectra of single‐crystal samples show the presence of the only trans conformer, as confirmed by X‐ray measurements. Finally, Raman spectra of thin films, as those used for the memory device, were collected; samples just deposited from solution and after few hours from the deposition were analyzed. Following the evolution of selective spectroscopic Raman markers, an isomerization process from the abundant cis (as‐deposited) to the totally trans (after few hours) conformer in the solid phase was detected. These results open the way to the identification of the molecular isomers present in the thin film of the memory cell and finally of the active molecular species involved in the switching mechanism of the operating device. Copyright © 2009 John Wiley & Sons, Ltd. A combined theoretical and experimental Raman study is presented on a diphenyl bithiophene molecule known as a good candidate for organic nonvolatile memory devices. Spectroscopic markers suitable to distinguish the different stable conformers of the molecule have been predicted and detected, thus opening the way to the identification of the molecular isomers present in the thin film of the memory cell and finally of the active molecular species involved in the switching mechanism of the operating device.
doi_str_mv 10.1002/jrs.2449
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Spectroscopic markers suitable to distinguish the different stable conformers of the molecule have been predicted and detected. The combined analysis of theoretical and experimental Raman spectra recorded in solution indicates that at room temperature a dynamical equilibrium, characterized by interconversion between the two more stable conformers (namely trans and cis), takes place and that the more populated species is the cis form. Referring to the solid phase instead, Raman spectra of single‐crystal samples show the presence of the only trans conformer, as confirmed by X‐ray measurements. Finally, Raman spectra of thin films, as those used for the memory device, were collected; samples just deposited from solution and after few hours from the deposition were analyzed. Following the evolution of selective spectroscopic Raman markers, an isomerization process from the abundant cis (as‐deposited) to the totally trans (after few hours) conformer in the solid phase was detected. These results open the way to the identification of the molecular isomers present in the thin film of the memory cell and finally of the active molecular species involved in the switching mechanism of the operating device. Copyright © 2009 John Wiley &amp; Sons, Ltd. A combined theoretical and experimental Raman study is presented on a diphenyl bithiophene molecule known as a good candidate for organic nonvolatile memory devices. 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Raman Spectrosc</addtitle><description>A combined theoretical and experimental Raman study is presented on a diphenyl bithiophene molecule known as a good candidate for the development of organic nonvolatile memory devices. Spectroscopic markers suitable to distinguish the different stable conformers of the molecule have been predicted and detected. The combined analysis of theoretical and experimental Raman spectra recorded in solution indicates that at room temperature a dynamical equilibrium, characterized by interconversion between the two more stable conformers (namely trans and cis), takes place and that the more populated species is the cis form. Referring to the solid phase instead, Raman spectra of single‐crystal samples show the presence of the only trans conformer, as confirmed by X‐ray measurements. 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source Wiley Online Library Journals Frontfile Complete
subjects Data storage
Deposition
DFT
diphenyl bithiophene
isomerization process
Markers
Memory devices
Raman markers
Raman spectra
resistive organic memory
Solid phases
Spectroscopy
Thin films
title Raman spectroscopic characterization of a thiophene-based active material for resistive organic nonvolatile memories
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