Issue 29, 2015

Vibrational modes of aminothiophenol: a TERS and DFT study

Abstract

We report Tip Enhanced Raman Spectroscopy (TERS) mapping and Density Functional (DFT) calculations of aminothiophenol (ATP) grafted on a gold surface. The TERS mapping has demonstrated Raman modes of (ATP) and its dimerised derivative Dimercaptoazobenzene (DMAB). This feature confirms that the plasmon activated chemical reaction of ATP has occurred during TERS measurements. In some specific part of the samples some unidentified Raman modes are observed. We suggest that they could come from intermediate species formed during the conversion of ATP into DMAB. These modes are compared with calculated Raman spectra of some possible intermediate species. These results confirm the high potentiality of TERS measurements for nanochemistry.

Graphical abstract: Vibrational modes of aminothiophenol: a TERS and DFT study

Article information

Article type
Paper
Submitted
18 Mar 2015
Accepted
25 Jun 2015
First published
26 Jun 2015

Phys. Chem. Chem. Phys., 2015,17, 19134-19138

Author version available

Vibrational modes of aminothiophenol: a TERS and DFT study

A. Merlen, M. Chaigneau and S. Coussan, Phys. Chem. Chem. Phys., 2015, 17, 19134 DOI: 10.1039/C5CP01579K

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