Raman polarization studies of highly oriented organic thin films

In this work we report on the capability of polarized Raman spectroscopy to investigate the structure of thin organic films. Diindenoperylene (DIP) thin films on (1 × 1)‐rutile(110) were prepared via organic molecular beam deposition (OMBD). Raman spectra of DIP thin films showed several strong Rama...

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Published inJournal of Raman spectroscopy Vol. 40; no. 12; pp. 2015 - 2022
Main Authors Presser, V., Schuster, B.-E., Casu, M. B., Heinemeyer, U., Schreiber, F., Nickel, K. G., Chassé, T.
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.12.2009
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Summary:In this work we report on the capability of polarized Raman spectroscopy to investigate the structure of thin organic films. Diindenoperylene (DIP) thin films on (1 × 1)‐rutile(110) were prepared via organic molecular beam deposition (OMBD). Raman spectra of DIP thin films showed several strong Raman modes in the wavenumber region from 1200 to 1650 cm−1. The Ag mode at 1284 cm−1 shows two contributions, thereby indicating the coexistence of at least two DIP film structures. Polarized Raman spectroscopy was applied to characterize the molecular orientation and the dominance of the σ‐configuration (i.e. upright standing DIP molecules) was found. Copyright © 2009 John Wiley & Sons, Ltd. Polarized Raman spectroscopy is a powerful tool to investigate the structure of thin organic films. In the present study, diindenoperylene (DIP) thin films on (1 × 1)‐rutile(110) were prepared via organic molecular beam deposition (OMBD). As a result, the coexistence of at least two DIP film structures is indicated because of the contribution of two Raman modes. Polarized Raman spectra used to characterize the actual orientation showed that the DIP molecules are predominantly present in the so‐called σ‐configuration (i.e. upright standing).
Bibliography:istex:35309A85CA507872025AD8A62BC8E6FDA356D16B
ark:/67375/WNG-WKKR2C4M-V
ArticleID:JRS2361
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0377-0486
1097-4555
DOI:10.1002/jrs.2361